{"title":"Organoboron [Organometallic Reagents]","description":"\u003cp\u003e\u003cstrong\u003eOrganoboron [Organometallic Reagents]\u003c\/strong\u003e — mencakup asam boronat dan turunannya, reagen borilasi, serta senyawa organoboron lain yang menjadi mitra reaksi dalam pembentukan ikatan karbon-karbon. Golongan ini berperan sebagai blok bangun serbaguna dalam sintesis organik modern berbasis logam transisi.\u003c\/p\u003e\u003cp\u003eOrganoboron banyak dipakai dalam reaksi kopling Suzuki-Miyaura untuk merangkai cincin aromatik dan heteroaromatik pada sintesis obat, material fungsional, dan senyawa optoelektronik seperti fluoresen. Ester boronat dan asam boronat juga berfungsi sebagai reagen borilasi C-H serta prekursor untuk sintesis multi-tahap di laboratorium kimia organik dan pengembangan material.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510i073935983\"\u003eTCI I0739 685103-98-4 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)isoquinoline\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b558012243\"\u003eTCI B5580 620624-96-6 2-(7-Bromo-9,9-di-n-octyl-9H-fluoren-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510i078736050\"\u003eTCI I0787 80041-89-0 Isopropylboronic Acid (contains varying amounts of Anhydride)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b558812256\"\u003eTCI B5588 330793-01-6 N-(tert-Butoxycarbonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510i083336115\"\u003eTCI I0833 61676-61-7 2-Isopropoxy-4,4,6-trimethyl-1,3,2-dioxaborinane\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b565612352\"\u003eTCI B5656 728911-52-2 2,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9,9'-spirobi[9H-fluorene]\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510i086436156\"\u003eTCI I0864 89787-12-2 (2-Isopropylphenyl)boronic Acid (contains varying amounts of Anhydride)\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b570312416\"\u003eTCI B5703 398128-09-1 2,2'-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,1'-biphenyl\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePilih berdasarkan kestabilan terhadap udara dan kelembapan, karena sejumlah asam boronat mengandung anhidrida dalam jumlah bervariasi, serta perhatikan gugus pelindung diol seperti pinakol yang memengaruhi reaktivitas kopling. Seluruh produk merupakan produk asli Tokyo Chemical Industry (TCI) Jepang, dengan kemurnian, kemasan, dan kondisi penyimpanan tercantum pada halaman masing-masing item.\u003c\/p\u003e\u003cp\u003eKategori lain yang sejajar di bawah Organometallic Reagents, sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-organosilicon-organometallic-reagents\"\u003eOrganosilicon [Organometallic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-grignard-reagents\"\u003eGrignard Reagents\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-organotin-organometallic-reagents\"\u003eOrganotin [Organometallic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-organotins-other-organometallic-reagents\"\u003eOrganotins (Other) [Organometallic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-organoarsenic-organometallic-reagents\"\u003eOrganoarsenic [Organometallic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-organoselenium-organometallic-reagents\"\u003eOrganoselenium [Organometallic Reagents]\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKoleksi ini masih terbagi menjadi 3 kelompok yang lebih spesifik:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-boronic-acids-and-derivatives-organoboron\"\u003eBoronic Acids and Derivatives [Organoboron]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-organoboron-compounds-other-organoboron\"\u003eOrganoboron Compounds (Other) [Organoboron]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-borylation-reagents-organoboron\"\u003eBorylation Reagents [Organoboron]\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l2-organometallic-reagents\"\u003eOrganometallic Reagents\u003c\/a\u003e. Untuk pengadaan volume besar, kemasan khusus, atau grade tertentu, hubungi tim AMI Scientific — distributor resmi TCI Japan di Indonesia — untuk pengecekan ketersediaan dan lead time langsung ke Jepang.\u003c\/p\u003e","products":[{"product_id":"tci2510b558012243","title":"TCI B5580 620624-96-6 2-(7-Bromo-9,9-di-n-octyl-9H-fluoren-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5580 is an organoboron reagent featuring a 9,9-di-n-octylfluorene core with a bromo substituent at the 7-position and a reactive dioxaborolane group, serving as a versatile building block for Suzuki-Miyaura cross-coupling reactions. This compound is widely employed in the synthesis of functional organic materials, including OLED emitters, organic photovoltaics, and conjugated polymers for optoelectronic applications. Its well-defined structure and reliable reactivity make it a valuable precursor for constructing fluorene-based molecular architectures in academic and industrial research settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085887975642,"sku":"TCI2510B558012243","price":3508000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5580.jpg?v=1769180197"},{"product_id":"tci2510b558812256","title":"TCI B5588 330793-01-6 N-(tert-Butoxycarbonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eN-(tert-Butoxycarbonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline is a versatile organoboron reagent featuring a Boc-protected aniline coupled with a pinacol boronate ester, primarily utilized as a key building block in Suzuki-Miyaura cross-coupling reactions. This compound enables the efficient synthesis of biaryl amine derivatives, which are essential structural motifs in medicinal chemistry and drug discovery programs. Its dual functionality — a protected amine and a reactive boronate — makes it an ideal intermediate for multi-step organic syntheses requiring orthogonal reactivity.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085889351898,"sku":"TCI2510B558812256","price":1036000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085889384666,"sku":"TCI2510B558812257","price":3560000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5588.jpg?v=1768204428"},{"product_id":"tci2510b565612352","title":"TCI B5656 728911-52-2 2,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9,9'-spirobi[9H-fluorene]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5656 (CAS 728911-52-2) is a spirobifluorene-based organoboron reagent featuring two pinacol boronate ester groups, making it an excellent building block for Suzuki-Miyaura cross-coupling reactions. Its rigid, orthogonal spirobifluorene core imparts high thermal stability and effectively suppresses intermolecular aggregation, which is highly desirable in organic optoelectronic applications. This compound is widely employed in the synthesis of OLED materials, fluorescent sensors, organic semiconductors, and porous organic frameworks.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085894299866,"sku":"TCI2510B565612352","price":3584000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5656.jpg?v=1768204431"},{"product_id":"tci2510b570312416","title":"TCI B5703 398128-09-1 2,2'-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,1'-biphenyl","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,2'-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,1'-biphenyl is a bifunctional organoboron reagent widely employed in Suzuki-Miyaura cross-coupling reactions to construct biaryl linkages with high efficiency. It serves as a versatile building block in the synthesis of conjugated polymers, advanced organic materials, and fluorescent probes. This compound is also utilized in medicinal and agrochemical research for elaborating substituted biphenyl cores in biologically active molecules.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085898166490,"sku":"TCI2510B570312416","price":1944000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085898199258,"sku":"TCI2510B570312417","price":6714000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5703.jpg?v=1769180217"},{"product_id":"tci2510b570412418","title":"TCI B5704 850264-92-5 3,3'-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,1'-biphenyl","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5704 (CAS 850264-92-5), 3,3'-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,1'-biphenyl, is a bifunctional organoboron reagent designed for Suzuki-Miyaura cross-coupling reactions, particularly in the construction of biphenyl-based conjugated polymers and porous organic frameworks. Its dual pinacol boronate ester groups at the meta positions enable stepwise or simultaneous carbon-carbon bond formation with aryl halides under palladium catalysis. This compound finds broad utility in the synthesis of COFs, MOFs, optoelectronic materials, and advanced functional polymers for research and development applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085898232026,"sku":"TCI2510B570412418","price":1666000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085898264794,"sku":"TCI2510B570412419","price":5755000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5704.jpg?v=1768204435"},{"product_id":"tci2510b577012507","title":"TCI B5770 1416243-42-9 2-[10-([1,1'-Biphenyl]-4-yl)anthracen-9-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5770 is an organoboron reagent featuring a dioxaborolane functional group coupled with a biphenyl-anthracene scaffold, primarily utilized in Suzuki-Miyaura cross-coupling reactions for constructing complex aromatic molecular architectures. This compound serves as a valuable building block in the synthesis of optoelectronic materials, including OLED emitters and organic semiconductors, owing to the favorable photophysical properties of its anthracene core. It is also widely employed in medicinal chemistry research for the preparation of substituted aromatic compound libraries with potential pharmaceutical applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085901902042,"sku":"TCI2510B577012507","price":3686000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5770.jpg?v=1768204441"},{"product_id":"tci2510b577412513","title":"TCI B5774 5,10-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)naphtho[1,2-c:5,6-c']bis([1,2,5]oxadiazole)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5774 is a bis(pinacolatoboron)-functionalized naphtho-bisoxadiazole compound serving as a versatile diboron reagent for Suzuki-Miyaura cross-coupling reactions. This compound acts as a dual-functional building block for constructing π-conjugated polymers and small-molecule optoelectronic materials. It is particularly valuable in research involving OLEDs, organic photovoltaics, and fluorescent sensors due to the electron-accepting character of the oxadiazole core.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48085902131418,"sku":"TCI2510B577412513","price":9767000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5774.jpg?v=1769180228"},{"product_id":"tci2510b582112570","title":"TCI B5821 171364-86-6 2-(Benzo[b]thiophen-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5821, with the CAS number 171364-86-6, is a highly specialized organoboron compound known as 2-(Benzo[b]thiophen-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane. This reagent plays a crucial role in the field of organometallic chemistry, particularly in synthetic processes that require precise and efficient chemical transformations. It is widely used in laboratories for its ability to participate in various coupling reactions, making it an essential tool for chemists working on complex molecule synthesis. Its unique structure combines a benzo[b]thiophen-3-yl group with a tetramethyl-dioxaborolane core, enabling it to interact effectively with transition metals in catalytic systems.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its stability under controlled laboratory conditions and its reactivity in a variety of chemical environments. These properties make it a preferred choice for researchers aiming to achieve high yields and consistent results in synthetic reactions. Its compatibility with a range of catalysts and its ability to undergo selective transformations contribute to its widespread use in advanced chemical applications. Additionally, the compound's versatility allows it to be adapted to different synthetic strategies, enhancing its utility in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is commonly used in organic chemistry research, especially in pharmaceutical development, material science, and environmental chemistry. Its reliability and effectiveness in promoting efficient chemical reactions make it a vital component in the toolkit of chemists working on innovative projects. Its application in these fields underscores its importance in advancing scientific discovery and technological development in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis for creating complex molecular structures due to its reactivity in coupling reactions.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research for developing new drugs through efficient synthetic pathways involving organoboron reagents.\u003c\/li\u003e\n\u003cli\u003eMaterial science applications in the production of advanced polymers and functional materials.\u003c\/li\u003e\n\u003cli\u003eEnvironmental chemistry studies for the synthesis of compounds used in pollution control and remediation.\u003c\/li\u003e\n\u003cli\u003eCatalytic processes in industrial settings where transition metal-based reactions are required for high efficiency.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 171364-86-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory reagent packaging\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the specific formulation and packaging\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry, and well-ventilated area away from direct sunlight and sources of heat. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and maintain chemical integrity. Due to its reactivity with moisture and air, it should be handled in a fume hood when possible, and appropriate personal protective equipment should be worn. Regular monitoring of storage conditions is essential to ensure the compound remains stable and effective for laboratory use. Always follow standard safety protocols to minimize exposure and ensure safe handling in a controlled environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085905047770,"sku":"TCI2510B582112570","price":4013000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5821.jpg?v=1768204445"},{"product_id":"tci2510b582312573","title":"TCI B5823 519054-55-8 2-(Benzofuran-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-(Benzofuran-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron compound widely used in organic chemistry laboratories for its versatility in chemical reactions. This reagent plays a crucial role in the synthesis of complex organic molecules, particularly in the development of heterocyclic and aromatic compounds. Its unique structure, containing a boron atom, makes it an essential component in various synthetic pathways. Due to its reactivity and stability under controlled conditions, it is a go-to reagent for researchers aiming to create intricate molecular structures.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical properties, including its reactivity in coupling reactions like the Suzuki-Miyaura reaction, make it a preferred choice for synthetic chemists. The presence of the boron atom allows for efficient participation in substitution reactions and bond formation, enhancing the efficiency of synthetic processes. Its stability in certain conditions ensures that it remains viable for use in multiple experimental setups. These characteristics make it a reliable and effective reagent in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in the synthesis of heterocyclic and aromatic compounds. It is a key reagent in the development of pharmaceuticals, industrial chemicals, and other complex molecules. Many research institutions and universities in Indonesia rely on this compound for its ability to facilitate complex chemical transformations. Its application is widespread in both academic and applied research settings, supporting a variety of chemical investigations.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its reactivity in coupling reactions and structural versatility.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceuticals and industrial chemicals through efficient bond formation and substitution reactions.\u003c\/li\u003e\n\u003cli\u003eResearch in aromatic compound synthesis where stable and reactive reagents are required for complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eSupport for academic research in chemical engineering and medicinal chemistry for advanced synthetic pathways.\u003c\/li\u003e\n\u003cli\u003eUse in industrial applications for the production of specialty chemicals requiring precise and controlled chemical reactions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 519054-55-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry place, away from moisture and direct sunlight to maintain its stability and reactivity. It is recommended to use airtight containers to prevent exposure to air and humidity, which may affect its chemical integrity. General laboratory precautions include handling with care to avoid contamination and ensuring proper ventilation when working with it. Due to its reactivity, it should be stored separately from strong oxidizing agents and incompatible materials. Always follow standard safety protocols when handling organoboron compounds to ensure a safe laboratory environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48085905178842,"sku":"TCI2510B582312573","price":1237000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085905211610,"sku":"TCI2510B582312574","price":3660000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5823.jpg?v=1769180235"},{"product_id":"tci2510b584412603","title":"TCI B5844 885693-20-9 1-(tert-Butoxycarbonyl)-1,2,5,6-tetrahydro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5844 is a Boc-protected tetrahydropyridine boronate ester (CAS 885693-20-9) that serves as a versatile organoboron building block for Suzuki-Miyaura cross-coupling reactions. This compound is widely employed in medicinal chemistry and pharmaceutical research for constructing substituted pyridine derivatives and complex heterocyclic scaffolds. Available in 200 mg and 1 g pack sizes, it is an essential reagent for C–C bond formation in drug discovery and advanced organic synthesis.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085906260186,"sku":"TCI2510B584412603","price":1137000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085906292954,"sku":"TCI2510B584412604","price":3636000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5844.jpg?v=1768204447"},{"product_id":"tci2510b587112631","title":"TCI B5871 175361-81-6 2,5-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,5-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene is a bifunctional organoboron reagent featuring a thiophene core with two pinacol boronate ester groups. This compound serves as a key building block in Suzuki-Miyaura cross-coupling reactions, enabling the efficient incorporation of thiophene units into conjugated organic frameworks. It is widely utilized in the synthesis of organic semiconductors, conductive polymers, and advanced materials for optoelectronic applications such as organic solar cells and OLEDs.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085907341530,"sku":"TCI2510B587112631","price":1515000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085907374298,"sku":"TCI2510B587112632","price":5402000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5871.jpg?v=1768204450"},{"product_id":"tci2510b596012739","title":"TCI B5960 331958-92-0 2-(3-Buten-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (stabilized with Phenothiazine)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5960 2-(3-Buten-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a stabilized organoboron reagent (containing phenothiazine as stabilizer) widely employed in Suzuki-Miyaura cross-coupling reactions. This boronic ester serves as a versatile alkenyl building block for constructing complex organic molecules, particularly in pharmaceutical and medicinal chemistry research. Available in 1g and 5g packaging, the product delivers reliable performance for both small-scale trial reactions and multi-step synthetic workflows.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085911896282,"sku":"TCI2510B596012739","price":2273000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085911929050,"sku":"TCI2510B596012740","price":8051000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5960.jpg?v=1771058372"},{"product_id":"tci2510b599312778","title":"TCI B5993 1821433-54-8 N,N'-Bis(2-ethylhexyl)-6,6'-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)isoindigo","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5993 (CAS 1821433-54-8) is an isoindigo-based organoboron reagent featuring two pinacol boronate ester moieties, designed as a versatile building block for Suzuki-Miyaura cross-coupling reactions. Its electron-deficient isoindigo core makes it highly suitable for constructing donor-acceptor type conjugated polymers used in organic electronics. This compound is commonly employed in research and development of organic field-effect transistors (OFETs) and organic photovoltaic (OPV) materials.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085913632986,"sku":"TCI2510B599312778","price":5553000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5993.jpg?v=1768204463"},{"product_id":"tci2510b599412779","title":"TCI B5994 1563062-80-5 N,N'-Bis(2-octyldodecyl)-6,6'-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)isoindigo","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5994 is a high-purity isoindigo-based organoboron reagent equipped with two pinacol boronate ester functionalities and branched 2-octyldodecyl N-substituents for enhanced solubility in organic solvents. This bifunctional monomer is primarily used as a building block in Suzuki-Miyaura cross-coupling polymerization to construct donor-acceptor conjugated polymers. Its key applications lie in the field of organic electronics, including organic field-effect transistors (OFETs), organic photovoltaics (OPVs), and other advanced optoelectronic devices requiring narrow-bandgap semiconducting materials.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085913764058,"sku":"TCI2510B599412779","price":5200000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5994.jpg?v=1769144659"},{"product_id":"tci2510b599612780","title":"TCI B5996 1412448-63-5 2,5-Bis(2-decyltetradecyl)-3,6-bis[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophen-2-yl]pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eThis complex chemical compound is a specialized organoboron reagent used in advanced organic chemistry applications. It belongs to the class of organoboron compounds, which are widely utilized in synthetic chemistry for their unique reactivity and functional group compatibility. The compound's molecular structure features a pyrrolo[3,4-c]pyrrole core with multiple alkyl chains and boron-containing groups, making it suitable for a variety of chemical transformations. Its role in the laboratory is critical for synthesizing complex heterocyclic structures and facilitating coupling reactions that require precise control over reactivity and stability.\u003c\/p\u003e\n\u003cp\u003eThe compound's high reactivity and specificity make it a preferred choice for researchers working on intricate organic syntheses. Its ability to participate in substitution, coupling, and reduction reactions is enhanced by its solubility in organic solvents, which simplifies its use in laboratory procedures. Additionally, its molecular complexity allows it to interact with various functional groups, making it a versatile tool in the development of new chemical compounds. These properties make it an essential reagent for both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, particularly in the synthesis of heterocyclic compounds and complex molecular structures. Its unique chemical properties are leveraged in studies aimed at developing new pharmaceuticals, materials, and specialty chemicals. The compound's stability and reactivity make it a valuable asset in both academic and applied research environments, supporting the advancement of chemical sciences in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its ability to participate in coupling and substitution reactions.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceuticals and specialty chemicals through its reactivity with functional groups.\u003c\/li\u003e\n\u003cli\u003eResearch in materials science for the creation of advanced polymers and functional materials.\u003c\/li\u003e\n\u003cli\u003eSynthesis of complex molecular structures requiring precise control over reactivity and stability.\u003c\/li\u003e\n\u003cli\u003eSupport for industrial chemical processes that require efficient and reliable reagents with high functional versatility.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1412448-63-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: 2,5-Bis(2-decyltetradecyl)-3,6-bis[5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophen-2-yl]pyrrolo[3,4-c]pyrrole-1,4(2H,5H)-dione\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid (not specified)\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to moisture and air, which can affect its stability. Due to its reactivity, it should be handled in a well-ventilated area, ideally under a fume hood, to minimize any potential hazards. Avoid contact with incompatible materials such as strong oxidizing agents. Always use appropriate personal protective equipment, including gloves and safety goggles, when handling this compound. Proper storage and handling ensure the compound remains effective and safe for use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085913796826,"sku":"TCI2510B599612780","price":7319000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5996.jpg?v=1768204466"},{"product_id":"tci2510b600612794","title":"TCI B6006 950779-13-2 1,6-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,6-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrene is a highly specialized organoboron compound used in advanced chemical research. This compound plays a crucial role in synthetic chemistry, particularly in the development of complex molecular structures. Its unique structure, featuring boron-containing groups, makes it an essential reagent in various coupling reactions, such as Suzuki-Miyaura and Kumada-Corriu. Due to its reactivity and versatility, it is widely utilized in laboratories for creating aromatic compounds with specific functional groups.\u003c\/p\u003e\n\u003cp\u003eThe compound's organoboron functionality provides it with exceptional reactivity towards transition metals and organic compounds. This reactivity allows it to participate in a wide range of chemical transformations, making it a preferred choice for synthetic chemists. Its ability to form stable intermediates under controlled conditions enhances its utility in multi-step synthesis processes. The presence of the boron group also contributes to its stability in certain environments, which is vital for maintaining the integrity of the reaction pathway.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in the synthesis of aromatic compounds and drug development. Its availability in the local market ensures that researchers have access to high-quality reagents for their experiments. The compound is a valuable tool for those working on complex molecular structures and functional group modifications. Its application is particularly relevant in academic and industrial research settings where precision and reliability are essential.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of aromatic compounds with specific substituents due to its reactivity and compatibility with coupling reactions.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceutical compounds through the formation of complex molecular frameworks using boron-based intermediates.\u003c\/li\u003e\n\u003cli\u003eResearch in transition metal catalysis where the compound serves as a versatile coupling agent in various synthetic pathways.\u003c\/li\u003e\n\u003cli\u003ePreparation of functionalized pyrene derivatives for use in materials science and photonic applications.\u003c\/li\u003e\n\u003cli\u003eInvestigation of boron-based reaction mechanisms in both academic and industrial research environments.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 950779-13-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: 1 g, 5 g, 25 g\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and light exposure. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure proper ventilation in the laboratory when working with this material. Avoid contact with incompatible substances to prevent unwanted chemical reactions. Proper storage and handling practices are essential to ensure the safety of laboratory personnel and the integrity of the compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085914386650,"sku":"TCI2510B600612794","price":4468000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085914419418,"sku":"TCI2510B600612795","price":15093000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6006.jpg?v=1769144657"},{"product_id":"tci2510b602312818","title":"TCI B6023 912844-88-3 2-([1,1'-Biphenyl]-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6023 2-([1,1'-Biphenyl]-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron reagent in the form of a pinacol ester of 3-biphenylboronic acid, primarily utilized in Suzuki-Miyaura cross-coupling reactions for constructing carbon-carbon bonds. This compound introduces the biphenyl moiety into target molecules with high efficiency, making it a valuable building block in organic synthesis. It is widely applied in pharmaceutical development, functional organic material research, and medicinal chemistry laboratories requiring biphenyl-containing molecular architectures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085915336922,"sku":"TCI2510B602312818","price":733000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085915369690,"sku":"TCI2510B602312819","price":2297000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6023.jpg?v=1768204474"},{"product_id":"tci2510b602412820","title":"TCI B6024 594823-67-3 2-(3-Bromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-(3-Bromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a pinacol boronate ester widely used as a versatile building block in Suzuki-Miyaura cross-coupling reactions to construct biaryl structures. This compound readily participates in transition-metal-catalyzed carbon-carbon bond formations, making it valuable in the synthesis of pharmaceutical intermediates and functional organic materials. TCI provides this reagent in 1 g and 5 g packaging options, suitable for both small-scale research and preparative laboratory synthesis.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085915435226,"sku":"TCI2510B602412820","price":758000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085915467994,"sku":"TCI2510B602412821","price":2297000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6024.jpg?v=1768204473"},{"product_id":"tci2510b602612824","title":"TCI B6026 1073354-70-7 1-(tert-Butoxycarbonyl)-3,5-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-(tert-Butoxycarbonyl)-3,5-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole is a complex organic compound widely used in laboratory settings for its unique reactivity and structural versatility. This reagent plays a crucial role in organic synthesis, particularly in the development of heterocyclic compounds and boron-containing molecules. Its application spans various synthetic pathways, making it an essential tool for researchers working in advanced chemical processes. Due to its functional groups, it is especially valuable in metal-catalyzed reactions, contributing to the efficiency and selectivity of synthetic protocols.\u003c\/p\u003e\n\u003cp\u003eThe compound's structure includes both a boron-containing group and a tert-butoxycarbonyl moiety, which together provide stability and reactivity in a range of chemical environments. These properties make it a preferred choice for synthetic chemists seeking reliable and controllable reagents. The presence of the boron group allows it to participate in important coupling reactions, such as Suzuki-Miyaura and Kumada-Corriu, which are fundamental in the synthesis of complex organic molecules. Its chemical specificity ensures that it can be tailored for various synthetic applications without unwanted side reactions.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used by chemists and researchers in the fields of organic synthesis, pharmacology, and materials science. Its role in producing precise and controlled chemical outcomes makes it a valuable asset in both academic and industrial research settings. Its application is particularly relevant in projects requiring high levels of chemical accuracy and synthetic efficiency.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis: This compound is ideal for creating complex heterocyclic structures due to its boron functionality and reactivity.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research: It is used in the development of new drug compounds, especially those involving boron-containing moieties.\u003c\/li\u003e\n\u003cli\u003eMaterials science: It contributes to the synthesis of advanced materials with specific chemical properties and structural features.\u003c\/li\u003e\n\u003cli\u003eMetal-catalyzed coupling reactions: Its ability to participate in Suzuki-Miyaura and Kumada-Corriu reactions makes it suitable for these specialized synthetic methods.\u003c\/li\u003e\n\u003cli\u003eCustom compound preparation: It is a key reagent in the synthesis of tailored organic compounds for specific research needs.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1073354-70-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: As per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid (as per standard product description)\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from moisture and direct sunlight to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its stability. Due to its reactivity, it should be handled with appropriate laboratory safety measures, including the use of personal protective equipment. Proper ventilation is essential when working with this material to minimize inhalation risks. It is important to follow standard chemical handling protocols to ensure the safety of laboratory personnel and the integrity of the compound during storage and use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085915631834,"sku":"TCI2510B602612824","price":1162000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085915664602,"sku":"TCI2510B602612825","price":3989000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6026.jpg?v=1769180251"},{"product_id":"tci2510b605012851","title":"TCI B6050 5565-36-6 1,4-Benzenediboronic Acid Bis(neopentyl Glycol) Ester","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6050 1,4-Benzenediboronic Acid Bis(neopentyl Glycol) Ester is a high-purity organoboron reagent designed as a versatile building block for Suzuki-Miyaura cross-coupling reactions. The bis(neopentyl glycol) ester protection on both boronic acid groups provides enhanced stability against moisture and oxidation while maintaining excellent reactivity under standard coupling conditions. This compound is widely employed in the synthesis of substituted biphenyls, conjugated polymers, metal-organic frameworks (MOFs), covalent organic frameworks (COFs), and pharmaceutical intermediates.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085916680410,"sku":"TCI2510B605012851","price":1970000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6050.jpg?v=1768204479"},{"product_id":"tci2510b655213480","title":"TCI B6552 2763205-15-6 2',7'-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)spiro[cyclopenta[2,1-b:3,4-b']dipyridine-5,9'-fluorene]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6552 is a spiro-linked building block bearing two pinacol boronate groups at the 2' and 7' positions of a spiro[cyclopenta-dipyridine-fluorene] framework. Its difunctional boronate handles make it a convenient monomer for palladium-catalysed Suzuki–Miyaura cross-coupling and for the assembly of conjugated oligomers and polymers. The rigid, orthogonal spiro geometry combined with electron-poor pyridine nitrogens is of particular interest in organic optoelectronic material research and in nitrogen-donor ligand design. AMI Scientific supplies this TCI product in 100 mg and 500 mg pack sizes; always consult the official TCI documentation and safety data sheet before use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48085946859738,"sku":"TCI2510B655213480","price":1970000.0,"currency_code":"IDR","in_stock":true},{"title":"500mg","offer_id":48085946892506,"sku":"TCI2510B655213481","price":6840000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6552.jpg?v=1767093890"},{"product_id":"tci2510b698413859","title":"TCI B6984 2378498-93-0 7-Bromo-2,12-di-tert-butyl-5,9-dioxa-13b-boranaphtho[3,2,1-de]anthracene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6984 7-Bromo-2,12-di-tert-butyl-5,9-dioxa-13b-boranaphtho[3,2,1-de]anthracene (CAS 2378498-93-0) is a brominated boron–oxygen fused polycyclic building block used in advanced materials chemistry. The rigid, planar boron-containing framework is a well-known motif in the development of narrowband multi-resonance emitters. Its bromo handle enables palladium-catalysed cross-coupling and amination to install tailored donor or acceptor units. AMI Scientific supplies this organoboron reagent in a 250 mg research-scale pack for Indonesian laboratories.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48085963309274,"sku":"TCI2510B698413859","price":3636000.0,"currency_code":"IDR","in_stock":true}]},{"product_id":"tci2510c200416625","title":"TCI C2004 346656-42-6 2-(2-Chlorophenyl)-5,5-dimethyl-1,3,2-dioxaborinane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-(2-Chlorophenyl)-5,5-dimethyl-1,3,2-dioxaborinane, also known as TCI C2004, is an organoboron compound widely used in organic synthesis. This reagent plays a crucial role in modern laboratory settings, particularly in the development of complex molecular structures. Its unique chemical structure enables highly specific and efficient reactions, making it a valuable tool for chemists. The compound is especially important in catalytic processes where precision and control over reaction pathways are essential.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical properties make it a preferred choice for various synthetic applications. It exhibits high reactivity, allowing the formation of new bonds with a wide range of organic substrates. Its stability under certain conditions ensures reliable performance in controlled environments, while its sensitivity to moisture and oxidation necessitates careful handling. These characteristics make it ideal for use in advanced synthetic methodologies that demand both accuracy and reproducibility.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is commonly used by chemists and researchers in the fields of pharmaceuticals and materials science. Its availability in the local market supports ongoing research and development efforts. The compound is particularly favored for its role in precision-driven chemical reactions, contributing to the advancement of scientific studies in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003eSuzuki-Miyaura Coupling Reactions\u003c\/strong\u003e: This reagent is ideal for forming carbon-carbon bonds in aromatic compounds, offering high efficiency and selectivity in cross-coupling processes.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eKumada-Corriu Coupling Reactions\u003c\/strong\u003e: It enables the synthesis of complex heterocyclic structures, providing a reliable method for creating new molecular frameworks.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eOrganic Synthesis of Aromatic Compounds\u003c\/strong\u003e: Its reactivity allows for the precise construction of aromatic rings, making it essential in the development of pharmaceutical intermediates.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eMaterial Science Research\u003c\/strong\u003e: The compound is used to create novel materials with specific chemical properties, supporting innovation in polymer and nanomaterial development.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003ePharmaceutical Compound Development\u003c\/strong\u003e: Its role in forming stable and functional chemical bonds makes it a key component in the synthesis of drug candidates and bioactive molecules.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 346656-42-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard supplier offerings\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on formulation and supplier\u003c\/li\u003e\n\u003cli\u003eStorage note: Requires dry, cool, and well-ventilated conditions to prevent degradation\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a dry, cool, and well-ventilated area to prevent moisture-induced degradation. It is recommended to use airtight containers made of glass or high-density polyethylene to minimize exposure to air and humidity. Due to its sensitivity to oxidation, it should be kept away from strong oxidizing agents and direct light. Proper personal protective equipment, including gloves and safety goggles, should always be worn when handling the material. Regular monitoring of storage conditions is essential to maintain its chemical integrity and ensure safe laboratory practices.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086095233242,"sku":"TCI2510C200416625","price":3963000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2004.jpg?v=1768197172"},{"product_id":"tci2510c206616716","title":"TCI C2066 162607-18-3 5-Chloro-2-thiopheneboronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C2066 is 5-Chloro-2-thiopheneboronic Acid containing varying amounts of anhydride (boroxine), a heteroaromatic organoboron reagent developed specifically for carbon–carbon bond formation. In modern synthetic laboratories, boronic compounds of this type serve as the principal nucleophilic partner in Suzuki-Miyaura cross-coupling reactions, allowing a chlorine-substituted thiophene ring to be joined to a wide range of aryl and heteroaryl halides. This capability makes the reagent an important tool for researchers constructing conjugated molecules for organic electronics as well as pharmaceutical scaffolds that incorporate thiophene units.\u003c\/p\u003e\n\u003cp\u003eThe most notable property of this material is the reactivity of the boronic acid group at position 2 of the thiophene ring, combined with the chlorine atom at position 5 that survives the coupling step and remains available for subsequent functionalisation. It should be understood that boronic acids naturally undergo partial dehydration to form the cyclic trimeric anhydride; for that reason the product label honestly states the presence of a varying anhydride content. This does not diminish its usefulness in coupling reactions, although researchers should allow for a slight excess of reagent when calculating stoichiometry.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used by university research groups, pharmaceutical chemistry teams, and materials science laboratories that carry out palladium-catalysed cross-coupling work. It is commonly drawn on during postgraduate synthesis projects, in the preparation of thiophene-containing intermediates, and in the development of conjugated materials, where a reliably supplied heteroaromatic boronic acid removes the need for in-house preparation of the building block.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSuzuki-Miyaura cross-coupling — the boronic acid at position 2 acts as the nucleophilic partner with aryl and heteroaryl halides under palladium catalysis, forming carbon–carbon bonds reliably.\u003c\/li\u003e\n\u003cli\u003eOrganic electronic materials synthesis — thiophene units are central to conjugated systems, so this reagent lets researchers install a chlorothiophene fragment into extended pi-conjugated backbones.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical scaffold construction — many drug candidates contain thiophene rings, and this building block introduces that motif directly into medicinal chemistry intermediates during discovery work.\u003c\/li\u003e\n\u003cli\u003eSequential functionalisation strategies — the chlorine at position 5 is retained through coupling, so it can be activated later for a second, independent bond-forming step.\u003c\/li\u003e\n\u003cli\u003eHeteroaromatic building-block library preparation — synthetic groups use this reagent to generate families of substituted thiophene derivatives for structure-activity screening and subsequent methodology studies.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 162607-18-3\u003c\/li\u003e\n\u003cli\u003eChemical name: 5-Chloro-2-thiopheneboronic Acid (contains varying amounts of Anhydride)\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the catalogue pack sizes offered by TCI for this item\u003c\/li\u003e\n\u003cli\u003eStorage note: keep tightly closed in a cool, dry place away from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the reagent in its original tightly closed container in a cool, dry area, protected from moisture and direct sunlight, since boronic acids readily undergo further dehydration to the anhydride form when exposed to humid air. Amber glass or the supplier's original packaging is suitable, and containers should be resealed promptly after each use. Weighing is best carried out quickly, or under an inert atmosphere where available. Handle in a fume hood using gloves, safety goggles, and a laboratory coat, avoid inhalation of dust, and keep the material separate from strong oxidising agents. Always consult the manufacturer's safety data sheet before use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086100869338,"sku":"TCI2510C206616716","price":1137000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086100902106,"sku":"TCI2510C206616717","price":3484000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2066.jpg?v=1767097751"},{"product_id":"tci2510c262117447","title":"TCI C2621 214360-48-2 2-(2-Cyanophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-(2-Cyanophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron compound widely used in organic chemistry for its versatile reactivity and structural stability. This compound plays a crucial role in various synthetic processes, particularly in the formation of heterocyclic compounds and aromatic derivatives. It is a key reagent in coupling reactions and Sadowksi-type reactions, where its ability to participate in selective transformations makes it indispensable in modern synthetic strategies. Its unique structure, featuring both a boron group and a cyano group, allows for precise functional group modifications in complex molecule synthesis.\u003c\/p\u003e\n\u003cp\u003eThe compound is preferred due to its controlled reactivity and high solubility in organic solvents, which simplifies handling and purification in laboratory settings. Its chemical stability ensures consistent performance across multiple reaction conditions, making it a reliable choice for researchers aiming for reproducibility and accuracy. The compound’s compatibility with a wide range of reaction conditions and its ability to undergo selective transformations further enhance its appeal in advanced synthetic applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is commonly used in organic chemistry research, especially in the synthesis of complex compounds and drug development. It is also employed in material science and environmental chemistry studies, where its participation in specific reaction pathways helps in the creation of compounds with desired structural properties. Its utility spans across multiple research fields, making it a valuable asset in both academic and industrial research environments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSadowksi Reactions for the synthesis of heterocyclic compounds due to its ability to undergo selective transformations and form stable intermediates.\u003c\/li\u003e\n\u003cli\u003eCoupling Reactions in organic synthesis where organoboron reagents are essential for efficient bond formation and functional group modification.\u003c\/li\u003e\n\u003cli\u003eDrug Development Research for the synthesis of complex aromatic derivatives and heterocyclic structures with specific biological activities.\u003c\/li\u003e\n\u003cli\u003eMaterial Science Studies for the creation of specialized compounds with unique structural and functional properties.\u003c\/li\u003e\n\u003cli\u003eEnvironmental Chemistry Applications for the synthesis of compounds that can be used in pollution control or remediation processes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 214360-48-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the specific formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers made of glass or polyethylene to protect it from moisture and air exposure. Due to its reactivity, it should be handled with care in a well-ventilated laboratory setting. Proper personal protective equipment, such as gloves and safety goggles, should be worn during handling. Avoid contact with incompatible materials and ensure that storage areas are free from potential contaminants. Regular monitoring of storage conditions is advised to ensure the compound remains in optimal condition for use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086143172826,"sku":"TCI2510C262117447","price":683000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086143205594,"sku":"TCI2510C262117448","price":2297000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2621.jpg?v=1768204684"},{"product_id":"tci2510c270717558","title":"TCI C2707 141091-37-4 2-(1-Cyclohexenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-(1-Cyclohexenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron compound widely used in modern organic synthesis. This reagent plays a crucial role in catalytic reactions, particularly in coupling reactions such as the Suzuki-Miyaura reaction. Its ability to facilitate the formation of complex molecules from simpler ones makes it indispensable in chemical laboratories. It is especially valuable for the synthesis of heterocyclic compounds and complex organic structures, which are common in pharmaceutical and materials research.\u003c\/p\u003e\n\u003cp\u003eThe compound’s unique molecular structure, containing a cyclohexene ring and a boron atom, contributes to its versatility in chemical reactions. Its stability under certain conditions and compatibility with transition metals like palladium make it a preferred choice for catalytic processes. Additionally, its capacity to undergo both electrophilic and nucleophilic activation allows it to be applied in a wide range of synthetic strategies. These properties make it a reliable and effective reagent for advanced chemical applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, pharmaceutical compound synthesis, and the development of new chemical materials. Its catalytic efficiency and broad applicability have made it a sought-after reagent among researchers and laboratories focused on innovation in chemical science. Its role in facilitating complex molecular transformations supports ongoing advancements in both academic and industrial chemical research.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003eSuzuki-Miyaura Coupling Reactions\u003c\/strong\u003e: This compound is ideal for coupling reactions due to its ability to activate and stabilize transition metal catalysts, enhancing reaction efficiency and selectivity.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eSynthesis of Heterocyclic Compounds\u003c\/strong\u003e: Its molecular structure enables the formation of complex ring systems, making it valuable in the creation of pharmaceutical and functional materials.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eOrganic Chemistry Research\u003c\/strong\u003e: It supports a wide range of synthetic strategies, contributing to the development of new chemical compounds and molecular architectures.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003ePharmaceutical Compound Development\u003c\/strong\u003e: Its role in catalytic processes aids in the synthesis of bioactive molecules, supporting drug discovery and development efforts.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eMaterial Science Applications\u003c\/strong\u003e: It is used in the synthesis of advanced materials, contributing to the creation of polymers and other functional chemical substances.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003eBrand\u003c\/strong\u003e: TCI\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eCAS Number\u003c\/strong\u003e: 141091-37-4\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eCategory\u003c\/strong\u003e: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003ePack Sizes\u003c\/strong\u003e: As per supplier specifications\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003ePhysical Form\u003c\/strong\u003e: Liquid\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eStorage Note\u003c\/strong\u003e: Store in a cool, dry place away from light and incompatible substances\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use sealed, airtight containers to prevent exposure to moisture and air. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure that it is stored separately from strong oxidizing agents and reactive materials to avoid any potential chemical interactions. Proper labeling and storage conditions help maintain its stability and effectiveness in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086192718042,"sku":"TCI2510C270717558","price":2550000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2707.jpg?v=1769144364"},{"product_id":"tci2510c282317696","title":"TCI C2823 214360-47-1 2-(2-Cyanophenyl)-5,5-dimethyl-1,3,2-dioxaborinane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-(2-Cyanophenyl)-5,5-dimethyl-1,3,2-dioxaborinane is an organoboron compound widely used in chemical reactions, especially in the synthesis of complex molecules. As a key reagent in organometallic chemistry, it plays a crucial role in facilitating carbon-carbon bond formation, which is fundamental in the development of pharmaceuticals and advanced materials. This compound is particularly valuable in coupling reactions, where its reactivity and compatibility with various ligands make it an essential tool for synthetic chemists. Its ability to participate in a range of reaction mechanisms enhances its versatility in laboratory settings.\u003c\/p\u003e\n\u003cp\u003eThe compound's high reactivity and compatibility with functional groups such as halides, alkoxides, and other ligands make it a preferred choice for chemists. Its organoboron structure allows for controlled reactivity, enabling the synthesis of a wide range of compounds with tailored properties. This characteristic is especially important in applications requiring precise molecular design. Additionally, its stability under certain reaction conditions ensures reliable performance, making it a trusted reagent in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used by researchers in universities and research institutions. It is particularly relevant in projects involving the synthesis of complex organic compounds, especially in the fields of pharmaceuticals and materials science. Its role in coupling reactions like the Suzuki-Miyaura reaction highlights its importance in modern synthetic methodologies. The availability of this compound supports advanced chemical research and innovation in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from its ability to form carbon-carbon bonds efficiently, supporting the creation of complex molecular structures.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes this compound in the development of new drug molecules due to its reactivity and compatibility with functional groups.\u003c\/li\u003e\n\u003cli\u003eMaterials science projects rely on its role in producing advanced polymers and functional materials through controlled coupling reactions.\u003c\/li\u003e\n\u003cli\u003eAcademic research in chemistry uses it as a key reagent for teaching and experimental studies in organometallic chemistry.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes incorporate it for the synthesis of specialty chemicals requiring precise molecular design and stability.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 214360-47-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid or solid, depending on supplier packaging\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from moisture and direct sunlight to maintain its chemical integrity. It is recommended to use airtight containers made of materials such as glass or polyethylene to prevent contamination and degradation. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment like gloves and safety goggles. It is important to ensure proper ventilation in the laboratory when working with this compound to minimize exposure. Always follow standard laboratory safety protocols to ensure safe handling and storage.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086198386906,"sku":"TCI2510C282317696","price":1086000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086198419674,"sku":"TCI2510C282317697","price":4115000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2823.jpg?v=1768204704"},{"product_id":"tci2510c292617824","title":"TCI C2926 419536-33-7 4-(9H-Carbazol-9-yl)phenylboronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-(9H-Carbazol-9-yl)phenylboronic Acid is a chemical compound widely used as a building block in the synthesis of complex organic molecules. This compound features a heterocyclic structure, combining a carbazole ring with a phenyl ring connected via a boronic acid group. Its unique molecular structure makes it a valuable resource for chemists working on the development of new compounds with specific biological activities. In laboratory settings, it plays a crucial role in synthetic chemistry, particularly in the creation of advanced pharmaceutical and material science applications.\u003c\/p\u003e\n\u003cp\u003eThe compound is favored for its stability and reactivity in various chemical reactions, especially those involving boron-based coupling reactions such as the Suzuki and Negishi reactions. These reactions are essential in the synthesis of complex organic structures, making this compound a preferred choice for researchers aiming to create functional molecules. Its ability to form stable bonds with different ligands enhances its versatility in synthetic applications, allowing for the design of compounds with tailored properties.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, particularly in the fields of pharmaceutical development and advanced material synthesis. Its structural complexity and chemical versatility make it an essential tool for scientists working on innovative projects. Due to its high reactivity and adaptability, it is a key component in the pursuit of new compounds with specific biological or functional properties.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis for the development of pharmaceutical compounds due to its reactivity in boron-based coupling reactions.\u003c\/li\u003e\n\u003cli\u003eCreation of advanced materials through the formation of complex molecular structures with high functional specificity.\u003c\/li\u003e\n\u003cli\u003eResearch in medicinal chemistry for the design of bioactive molecules with targeted biological effects.\u003c\/li\u003e\n\u003cli\u003eSynthesis of heterocyclic compounds, leveraging its unique carbazole and phenyl ring structure.\u003c\/li\u003e\n\u003cli\u003eUse in academic and industrial research settings for the exploration of new chemical functionalities and applications.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 419536-33-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent exposure to moisture and air, which could affect its reactivity. Due to its potential reactivity, it should be handled in a well-ventilated laboratory setting, using appropriate personal protective equipment such as gloves and safety goggles. Avoid contact with incompatible substances, and ensure proper disposal procedures are followed in accordance with local regulations. Regular monitoring of storage conditions is advised to ensure the compound remains in optimal condition for use in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086203334874,"sku":"TCI2510C292617824","price":1415000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086203367642,"sku":"TCI2510C292617825","price":4645000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2926.jpg?v=1767098992"},{"product_id":"tci2510c296717874","title":"TCI C2967 864377-33-3 3-(9H-Carbazol-9-yl)phenylboronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3-(9H-Carbazol-9-yl)phenylboronic Acid is a chemical compound widely used in laboratory settings for its versatility in organic synthesis. This compound plays a crucial role in the development of complex molecular structures, particularly in the field of heterocyclic chemistry. Its unique structure, combining a carbazole unit with a phenylboronic acid group, makes it a valuable building block for researchers aiming to create new compounds with specific functional properties. Due to its reactivity and compatibility with various functional groups, it is a key component in many synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eThe compound is preferred for its ability to participate in boronic acid-based reactions, such as Suzuki and Heck couplings, which are essential in the synthesis of pharmaceuticals and advanced materials. Its chemical stability under controlled conditions allows for reliable handling and storage, making it a dependable reagent in both academic and industrial research. Additionally, its capacity to form stable intermediates enhances its utility in multi-step synthesis processes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in the synthesis of heterocyclic compounds and drug development. It is a fundamental reagent for scientists working on molecular modifications and structural innovations. Its application spans across various research institutions and universities, supporting advancements in both academic and applied chemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its reactive boronic acid group and carbazole core.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research for the development of new drugs requiring complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eMolecular modification studies where precise functional group manipulation is essential.\u003c\/li\u003e\n\u003cli\u003eCoupling reactions such as Suzuki and Heck, which benefit from its stability and reactivity.\u003c\/li\u003e\n\u003cli\u003eAdvanced material synthesis for creating compounds with specific physical and chemical properties.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 864377-33-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep it in a sealed container to avoid exposure to moisture, which could affect its reactivity. Due to its potential for interaction with other substances, it should be handled in a well-ventilated area, preferably under a fume hood. Avoid direct contact with skin and eyes, and use appropriate personal protective equipment when handling. While no specific hazards are indicated, general laboratory safety practices should be followed to ensure safe usage and storage.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086205268186,"sku":"TCI2510C296717874","price":1187000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086205300954,"sku":"TCI2510C296717875","price":4165000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2967.jpg?v=1767099042"},{"product_id":"tci2510c299317906","title":"TCI C2993 172732-52-4 2-Cyanophenylboronic Acid 1,3-Propanediol Ester","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C2993 2-Cyanophenylboronic Acid 1,3-Propanediol Ester, CAS number 172732-52-4, is an organoboron reagent supplied as a cyclic boronate ester formed from 2-cyanophenylboronic acid and 1,3-propanediol. In organic synthesis laboratories, this compound serves as the nucleophilic partner in palladium-catalysed cross-coupling reactions, most notably the Suzuki–Miyaura coupling, which remains one of the principal methods for constructing carbon–carbon bonds. The cyano group in the ortho position adds further synthetic value, since it can subsequently be converted into amides, carboxylic acids, amines, or a variety of heterocyclic rings once the coupling step has been completed.\u003c\/p\u003e\n\u003cp\u003eThe main reason chemists select the propanediol ester form is its handling stability. Free boronic acids tend to form cyclic anhydrides (boroxines) readily, absorb moisture, and show a purity that is difficult to establish with certainty. The cyclic boronate ester, by contrast, is more resistant to humidity, is generally a solid that is easy to weigh out, and gives more accurate reaction stoichiometry. The ester can still undergo hydrolysis within the reaction medium, releasing the active boron species when it is required, so protection during storage does not come at the cost of reactivity during the coupling itself.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories this reagent fits the routine work of university organic synthesis groups, government research institutes, and pharmaceutical or fine chemical development units where biaryl and substituted aromatic scaffolds are prepared. Its moisture resistance is particularly relevant under Indonesian ambient humidity, where free boronic acids degrade more quickly on the bench. The ability to carry an ortho cyano handle through a coupling step and then elaborate it further makes the material useful for multi-step route development.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSuzuki–Miyaura cross-coupling: the compound acts as the organoboron nucleophile that transfers the 2-cyanophenyl group to an aryl or heteroaryl halide under palladium catalysis, forming the carbon–carbon bond directly.\u003c\/li\u003e\n\u003cli\u003eBiaryl scaffold construction: it introduces an ortho-substituted aromatic ring bearing a cyano group, allowing the assembly of substituted biaryl frameworks that are common targets in synthetic organic chemistry programmes.\u003c\/li\u003e\n\u003cli\u003eHeterocycle synthesis: the ortho cyano group can be cyclised after the coupling step, giving access to a variety of heterocyclic ring systems built onto the newly formed aromatic linkage.\u003c\/li\u003e\n\u003cli\u003eFunctional group elaboration studies: after coupling, the nitrile can be converted into amides, carboxylic acids, or amines, making this reagent suitable for multi-step route development and intermediate diversification.\u003c\/li\u003e\n\u003cli\u003eAccurate stoichiometric coupling work: because the ester form resists boroxine formation and moisture uptake, it is well suited to reactions where precise molar ratios of the boron partner must be maintained.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 172732-52-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003eChemical class: cyclic boronate ester of 2-cyanophenylboronic acid with 1,3-propanediol\u003c\/li\u003e\n\u003cli\u003ePhysical form: generally supplied as a solid that is convenient to weigh\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard TCI catalogue pack sizes for this item\u003c\/li\u003e\n\u003cli\u003eStorage: keep tightly closed in a cool, dry place away from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry, well-ventilated area, away from moisture, direct sunlight, and sources of ignition. Although the cyclic boronate ester is more resistant to humidity than the corresponding free boronic acid, prolonged exposure to atmospheric moisture should still be avoided; the original tightly sealed supplier container, or a well-closed glass vessel kept in a desiccator, is appropriate. Weigh the solid in a fume hood or a well-ventilated area, and wear safety glasses, gloves, and a laboratory coat. Avoid dust formation, inhalation, and contact with skin and eyes. Handle under an inert atmosphere where the downstream coupling reaction requires it, close the container immediately after use, and consult the manufacturer's safety data sheet before working with the material.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086206480602,"sku":"TCI2510C299317906","price":733000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086206513370,"sku":"TCI2510C299317907","price":2221000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2993.jpg?v=1769144337"},{"product_id":"tci2510c310118058","title":"TCI C3101 87100-15-0 2-Cyclohexyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Cyclohexyl-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile organoboron compound widely used in chemical synthesis, particularly in reactions involving carbon-carbon bond formation. As a key reagent in the field of organometallic chemistry, it plays a crucial role in enabling the creation of stable and diverse carbon structures. This compound is essential for researchers seeking to develop complex organic molecules with high precision and efficiency. Its unique molecular structure allows it to participate in a variety of reaction mechanisms, making it a valuable asset in both academic and industrial laboratory settings.\u003c\/p\u003e\n\u003cp\u003eThe compound's properties, such as its ability to form stable complexes with transition metals and its reactivity in substitution and catalytic reactions, make it a preferred choice for advanced chemical applications. The presence of cyclohexyl and tetramethyl groups enhances its stability and reactivity under different reaction conditions. These characteristics enable it to function effectively in a wide range of synthetic pathways, contributing to the success of many chemical processes. Its specificity and effectiveness in catalytic systems further solidify its importance in modern organic chemistry.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in research related to organic synthesis, pharmaceutical development, and material science. Its high reactivity and stability make it suitable for various experimental setups, especially in the context of green chemistry and sustainable synthesis methods. As a result, it is a key reagent in many research projects aimed at creating new compounds with specific functional properties.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from this compound's ability to form carbon-carbon bonds efficiently, making it ideal for creating complex organic structures.\u003c\/li\u003e\n\u003cli\u003eIn pharmaceutical research, it is used to develop new drug molecules by enabling the formation of stable and functional carbon frameworks.\u003c\/li\u003e\n\u003cli\u003eMaterial science experiments rely on its reactivity and stability to synthesize advanced polymers and functional materials with precise properties.\u003c\/li\u003e\n\u003cli\u003eCatalytic reactions in industrial settings utilize its capacity to interact with transition metals, enhancing reaction efficiency and selectivity.\u003c\/li\u003e\n\u003cli\u003eGreen chemistry initiatives incorporate this compound due to its low environmental impact and high reusability in sustainable synthesis processes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 87100-15-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Liquid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to use airtight containers made of materials that are chemically inert to avoid any unwanted reactions. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Avoid exposure to heat and direct light to ensure long-term preservation. In laboratory settings, it is important to follow standard safety protocols to minimize risks associated with its chemical properties. Proper labeling and storage conditions are essential to ensure safe handling and effective use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086213984474,"sku":"TCI2510C310118058","price":1313000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086214017242,"sku":"TCI2510C310118059","price":4518000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3101.jpg?v=1768204730"},{"product_id":"tci2510c312618085","title":"TCI C3126 741709-63-7 2-Cyano-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI 2-Cyano-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine, supplied under catalogue code C3126, is an organoboron compound consisting of a pinacol boronate ester attached to a cyano-substituted pyridine ring. It functions as a key reagent in carbon–carbon bond forming reactions, most notably the Suzuki–Miyaura cross-coupling, which stands as one of the most important methods available in modern synthetic chemistry. Within the laboratory, its role is to deliver the cyanopyridine fragment onto a target molecule through a palladium-catalysed reaction with a partnering aryl halide or triflate, allowing chemists to construct biaryl and heterobiaryl frameworks under reliable, well-documented conditions.\u003c\/p\u003e\n\u003cp\u003eThe pinacol ester form is chosen because it offers considerably better stability than the corresponding free boronic acid, an advantage that matters especially for heteroaromatic derivatives such as pyridines, which are well known to be prone to protodeboronation. The pinacol ester exists as a solid that is easier to weigh accurately, to store, and to purify, while still providing adequate reactivity under standard coupling conditions. The cyano group at the two position not only influences the electronic character of the ring but also serves as a synthetic handle that can later be converted into an amide, a carboxylic acid, a primary amine, or a tetrazole, so that a single reagent opens several downstream routes from one coupling step.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used in medicinal chemistry and organic synthesis research groups at universities and research institutes, as well as in pharmaceutical development laboratories building heterocyclic scaffolds. It suits work where a pyridine-containing fragment must be introduced into a larger structure, including analogue synthesis programmes, materials chemistry projects, and postgraduate research on cross-coupling methodology. The solid, stable ester form is convenient for laboratories that need a reagent tolerant of routine handling and ordinary storage practice.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSuzuki–Miyaura cross-coupling: the pinacol boronate transmetalates efficiently to palladium, transferring the cyanopyridyl group to aryl halides or triflates under standard base and catalyst conditions.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry analogue synthesis: introduces a cyanopyridine motif into candidate scaffolds, giving structure–activity relationship work a reliable route to heterobiaryl variants from common halide intermediates.\u003c\/li\u003e\n\u003cli\u003eHeterobiaryl scaffold construction: joins pyridine rings to other aromatic partners in one catalytic step, avoiding lengthy ring-building sequences that would otherwise be required for these frameworks.\u003c\/li\u003e\n\u003cli\u003eDownstream nitrile functionalisation: the two-position cyano group is converted after coupling into amides, carboxylic acids, primary amines, or tetrazoles, extending one reagent across several synthetic routes.\u003c\/li\u003e\n\u003cli\u003eCross-coupling methodology research: serves as a stable heteroaryl boron substrate for studying ligand, base, and catalyst effects where free boronic acids would suffer protodeboronation.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eCatalogue code: C3126\u003c\/li\u003e\n\u003cli\u003eCAS number: 741709-63-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePhysical form: solid pinacol boronate ester\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard research-scale pack sizes offered for this catalogue item\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a cool, dry place in the tightly closed original container\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container tightly closed in a cool, dry, well-ventilated area away from moisture, strong oxidising agents, and direct sunlight, and keep the material in its original supplier packaging or an equivalent tightly sealed glass or amber container. Because boronate esters are sensitive to prolonged moisture exposure, allow cold-stored material to reach room temperature before opening to prevent condensation, and reseal promptly after weighing. Handle in a fume hood using safety goggles, chemical-resistant gloves, and a laboratory coat, weigh the solid carefully to limit dust generation, and consult the manufacturer's safety data sheet before use and for disposal guidance.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086215000282,"sku":"TCI2510C312618085","price":733000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086215033050,"sku":"TCI2510C312618086","price":2778000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3126.jpg?v=1768204732"},{"product_id":"tci2510c324318235","title":"TCI C3243 286961-15-7 1-Carbobenzoxy-1,2,3,6-tetrahydro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eThis chemical compound, 1-Carbobenzoxy-1,2,3,6-tetrahydro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine, is a complex organoboron reagent widely used in organic synthesis. It plays a crucial role in laboratory settings, particularly in reactions that require precise control and high reactivity. As a key component in coupling reactions, it enables the formation of complex molecules with high specificity and efficiency. Its unique structure allows it to interact with various organic substrates, making it an essential tool for synthetic chemists.\u003c\/p\u003e\n\u003cp\u003eThe compound's properties make it a preferred choice for advanced chemical applications. It exhibits stable reactivity under controlled conditions, allowing for predictable and reproducible results. Its ability to form stable bonds with metals enhances its utility in catalytic processes. Additionally, its solid form simplifies handling and processing, making it suitable for use in both small-scale and large-scale experiments. These characteristics contribute to its reliability and effectiveness in laboratory environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, particularly in academic and research institutions. It is a key reagent in the development of complex synthetic pathways, supporting the creation of new compounds with specific functional groups. Its availability and performance make it a valuable resource for chemists working on advanced synthetic projects. The compound's versatility and efficiency have made it a standard in many laboratory workflows across Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions, especially in coupling processes like Suzuki-Miyaura and Kumada-Corriu, due to its reactivity and compatibility with various substrates.\u003c\/li\u003e\n\u003cli\u003eDevelopment of complex molecular structures requiring high specificity and controlled reactivity in synthetic pathways.\u003c\/li\u003e\n\u003cli\u003eCatalytic processes where the compound's ability to form stable metal bonds enhances reaction efficiency and selectivity.\u003c\/li\u003e\n\u003cli\u003eResearch in pharmaceutical and materials science, where precise chemical transformations are essential for compound development.\u003c\/li\u003e\n\u003cli\u003eTeaching and experimental applications in higher education institutions, supporting both theoretical and practical training in organic chemistry.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 286961-15-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from moisture and direct sunlight to maintain its stability and reactivity. It is recommended to use airtight containers to prevent exposure to air and humidity. As an organoboron reagent, it may react with moisture, so proper sealing is essential. Laboratory personnel should handle it with care, using appropriate personal protective equipment. It is important to ensure that the storage area is well-ventilated and free from incompatible materials. Regular inspection of storage conditions is advised to maintain the integrity of the compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086221914330,"sku":"TCI2510C324318235","price":2121000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086221947098,"sku":"TCI2510C324318236","price":7345000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3243.jpg?v=1769180439"},{"product_id":"tci2510c330118321","title":"TCI C3301 635305-24-7 5-Chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e5-Chloro-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene is a specialized chemical compound widely used in organic chemistry laboratories. It plays a crucial role in various synthetic processes, particularly in the development of heterocyclic compounds. This reagent is essential for facilitating coupling reactions, such as S-N coupling and the Suzuki-Miyaura reaction, which are fundamental in the synthesis of complex organic molecules. Its unique structure, incorporating both boron and chlorine functionalities, makes it a versatile tool in modern chemical research.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical properties, including its reactivity and stability under controlled conditions, make it a preferred choice for researchers. Its ability to participate in multiple reaction pathways enhances its utility in synthetic chemistry. The presence of the boronic acid group allows it to act as a key intermediate in cross-coupling reactions, which are vital for the creation of new compounds with specific biological or material properties. This reagent is especially valuable in applications requiring high selectivity and efficiency.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in pharmaceutical and materials science research. It is an essential component in the development of new drugs and advanced materials. Due to its complex molecular structure, it is often employed in studies aimed at understanding and improving the reactivity of organic compounds. Its application is widespread in academic and industrial settings, contributing to the advancement of scientific knowledge and innovation.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eUsed in pharmaceutical research for the synthesis of bioactive compounds due to its reactivity in coupling reactions.\u003c\/li\u003e\n\u003cli\u003eApplied in materials science for the development of new polymers and functional materials through cross-coupling processes.\u003c\/li\u003e\n\u003cli\u003eEmployed in synthetic organic chemistry for the preparation of heterocyclic compounds with specific structural features.\u003c\/li\u003e\n\u003cli\u003eUtilized in academic research for exploring new reaction mechanisms and synthetic pathways in organic chemistry.\u003c\/li\u003e\n\u003cli\u003eIntegrated into drug discovery programs to facilitate the construction of complex molecular frameworks with therapeutic potential.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 635305-24-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the specific formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Requires dry and cool storage to prevent moisture and oxidation\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a dry, cool environment away from moisture and oxidizing agents to maintain its chemical stability. It is recommended to use airtight containers made of inert materials such as glass or polyethylene to prevent exposure to humidity. Due to its sensitivity to moisture, handling should be done in a controlled atmosphere with appropriate safety measures. The compound should be kept in a well-ventilated area to minimize the risk of inhalation. Proper labeling and storage conditions are essential to ensure the integrity and safety of the material during laboratory use. Always follow standard laboratory safety protocols when working with this reagent.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086230630618,"sku":"TCI2510C330118321","price":986000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086230663386,"sku":"TCI2510C330118322","price":3434000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3301.jpg?v=1768204758"},{"product_id":"tci2510c335218389","title":"TCI C3352 1189047-28-6 2-(9H-Carbazol-9-yl)phenylboronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-(9H-Carbazol-9-yl)phenylboronic Acid is a chemical compound widely used in laboratory settings for its role in organometallic reactions and the synthesis of complex molecular structures. This reagent is particularly valued for its ability to participate in various chemical transformations, especially in catalytic processes that require precise control over reaction conditions. Its unique structure, combining a boronic acid group with a carbazole ring, makes it a versatile tool for chemists working on advanced synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eThe compound’s reactivity and specificity are enhanced by its molecular composition, which allows it to interact effectively in a range of chemical environments. Its stability under certain conditions, combined with its sensitivity to moisture and oxidation, requires careful handling to maintain its effectiveness. The presence of varying amounts of anhydride further influences its reactivity, making it a material that demands attention to storage and application protocols. These characteristics make it a reliable choice for researchers aiming to achieve high precision in their experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in the development of new compounds and molecular modifications. Its availability and consistent quality make it a preferred option for both academic and industrial research institutions. The compound is particularly useful in applications that require controlled chemical reactions, such as the Suzuki reaction, which is crucial in the synthesis of aromatic and heterocyclic compounds.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSuzuki Reaction for the synthesis of aromatic and heterocyclic compounds due to its reactivity and compatibility with palladium catalysts.\u003c\/li\u003e\n\u003cli\u003eOrganic synthesis of complex molecules requiring precise control over reaction conditions and functional group transformations.\u003c\/li\u003e\n\u003cli\u003eDevelopment of new pharmaceutical compounds through targeted molecular modifications and structural alterations.\u003c\/li\u003e\n\u003cli\u003eResearch in catalytic processes where boronic acid derivatives play a key role in cross-coupling reactions.\u003c\/li\u003e\n\u003cli\u003eInvestigation of chemical stability and reactivity under varying environmental conditions for academic and industrial studies.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1189047-28-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: 25g, 100g\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Keep in a dry, cool place away from moisture and oxidizing agents\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a dry, cool environment to prevent moisture-induced degradation and oxidation. It is recommended to use airtight containers made of glass or high-density polyethylene to maintain its chemical integrity. Due to its sensitivity to humidity, it should be handled in a controlled laboratory setting with appropriate ventilation. Avoid exposure to light and heat to preserve its reactivity. Always use appropriate personal protective equipment when handling this material to ensure safety during experiments. Proper storage and handling are essential to maintain its effectiveness in chemical reactions.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086236856538,"sku":"TCI2510C335218389","price":4518000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3352.jpg?v=1768204762"},{"product_id":"tci2510c335318390","title":"TCI C3353 858131-73-4 [4'-(Carbazol-9-yl)-4-biphenylyl]boronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e[4'-(Carbazol-9-yl)-4-biphenylyl]boronic Acid is a specialized organoboron compound used in organic chemistry laboratories. This reagent plays a critical role in various synthetic processes, particularly in the development of complex molecules with high reactivity. Its unique chemical structure allows it to participate in important reactions such as the Suzuki and Kumada couplings, which are essential for the synthesis of heteroaromatic compounds and polymers. Due to its versatility and effectiveness, it is a valuable tool for researchers working on advanced chemical synthesis.\u003c\/p\u003e\n\u003cp\u003eThe compound is preferred for its high reactivity and ability to form stable complexes with transition metals. These properties make it an ideal candidate for catalytic processes and functional group transformations. Its stability under certain conditions also ensures that it can be stored and used reliably over time, which is crucial for maintaining experimental consistency. Additionally, its purity and reactivity make it a trusted choice for precise and reproducible chemical experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is widely used in organic chemistry research, particularly in academic and industrial settings. It supports the development of new materials, pharmaceuticals, and advanced chemical products. Its application is especially relevant in institutions focused on chemical synthesis and innovation, where high-quality reagents are essential for reliable results.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis reactions, especially those involving Suzuki and Kumada couplings, due to its reactivity and compatibility with transition metals.\u003c\/li\u003e\n\u003cli\u003eDevelopment of heteroaromatic compounds and polymers, as it facilitates the formation of complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eCatalytic processes in chemical reactions, where its ability to form stable metal complexes enhances reaction efficiency.\u003c\/li\u003e\n\u003cli\u003eResearch in pharmaceutical and material sciences, where precise chemical transformations are required for compound development.\u003c\/li\u003e\n\u003cli\u003eAdvanced chemical synthesis projects in academic and industrial laboratories, where high purity and reactivity are essential for experimental success.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 858131-73-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, typically in powder or crystalline form\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its stability and reactivity. It is recommended to keep it in airtight containers to prevent exposure to moisture and air, which can affect its chemical integrity. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to store it away from incompatible substances to avoid any potential chemical reactions. In a laboratory setting, proper ventilation and adherence to standard safety protocols are essential when working with this compound to ensure safe and effective use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086236954842,"sku":"TCI2510C335318390","price":910000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086236987610,"sku":"TCI2510C335318391","price":3257000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3353.jpg?v=1768204763"},{"product_id":"tci2510c336718408","title":"TCI C3367 865186-94-3 3-Chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3-Chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a versatile organic compound widely used in laboratory settings for its unique chemical properties. This compound is a key building block in the synthesis of heterocyclic compounds, playing a crucial role in organic chemistry research. Its complex structure enables it to participate in various substitution and catalytic reactions, making it an essential reagent in the development of new chemical entities. It is particularly valuable in the field of medicinal chemistry and materials science due to its reactivity and functional group versatility.\u003c\/p\u003e\n\u003cp\u003eThe compound's reactivity is primarily attributed to its chloro and boronic acid functionalities, which make it highly compatible with a range of reagents. The boron-containing group allows for efficient coupling reactions, such as the Suzuki and Heck reactions, which are commonly used in the synthesis of complex molecules. This reactivity, combined with its structural stability, makes it a preferred choice for chemists working on advanced synthetic pathways. Its ability to form stable intermediates under controlled conditions further enhances its utility in laboratory applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is frequently used in organic synthesis projects, particularly in pharmaceutical and materials research. It is a common reagent in academic and industrial settings, where it supports the development of new drugs and advanced materials. Its use is widespread among research institutions and universities, contributing to the advancement of chemical sciences in the region. The compound's reliability and effectiveness make it a staple in modern chemical laboratories.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its reactivity and structural versatility.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research for the development of new drug molecules through coupling reactions.\u003c\/li\u003e\n\u003cli\u003eMaterials science applications in the creation of advanced polymers and functional materials.\u003c\/li\u003e\n\u003cli\u003eAcademic research in chemical engineering and medicinal chemistry for compound development.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes requiring efficient and reliable synthetic intermediates.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 865186-94-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder or liquid, depending on formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Due to its reactivity, it should be handled in a well-ventilated area, preferably under a fume hood. Avoid contact with incompatible substances such as strong oxidizers. Regularly check the container for any signs of degradation or contamination. Proper labeling and storage conditions are essential to ensure safety and maintain the compound's effectiveness in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086238494938,"sku":"TCI2510C336718408","price":758000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086238527706,"sku":"TCI2510C336718409","price":2399000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3367.jpg?v=1769144291"},{"product_id":"tci2510c338518428","title":"TCI C3385 287944-10-9 2-(1-Cyclopentenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-(1-Cyclopentenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron compound widely used in organic chemistry laboratories. It serves as a key reagent in various synthetic processes, particularly in catalytic reactions that form carbon-carbon bonds. This compound is especially valuable in the Suzuki-Miyaura coupling reaction, a critical method for the synthesis of heterocyclic compounds and complex organic molecules. Its role in facilitating efficient and selective bond formation makes it indispensable in modern synthetic chemistry.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its stable structure and controlled reactivity, allowing it to be used effectively under a variety of reaction conditions. Its high purity and solid form make it easy to handle and store, ensuring consistent performance in laboratory settings. Additionally, its moderate reactivity in its pure form means it can be safely stored and used without significant degradation, making it a reliable choice for both small-scale and large-scale experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is extensively used in organic chemistry research, particularly in the development of complex molecules and pharmaceutical compounds. Its stability and effectiveness make it a preferred reagent for researchers working on advanced synthetic pathways. The compound's availability in high purity and solid form further supports its widespread use in academic and industrial research settings.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSuzuki-Miyaura Coupling: This compound is ideal for coupling reactions due to its stability and controlled reactivity, enabling efficient carbon-carbon bond formation in complex molecule synthesis.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis of Heterocycles: Its unique structure allows it to participate in reactions that produce heterocyclic compounds, which are common in pharmaceutical and fine chemical applications.\u003c\/li\u003e\n\u003cli\u003eCatalytic Reactions in Industrial Chemistry: The compound's ability to function as a catalyst in various organic transformations makes it suitable for large-scale chemical production processes.\u003c\/li\u003e\n\u003cli\u003eResearch in Pharmaceutical Development: It is frequently used in the synthesis of drug molecules, supporting the creation of new therapeutic agents through selective bond formation.\u003c\/li\u003e\n\u003cli\u003eAdvanced Organic Chemistry Studies: Its role in creating complex molecular structures makes it a valuable tool for academic research in synthetic organic chemistry.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 287944-10-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from moisture and direct sunlight to maintain its stability and reactivity. It is recommended to use airtight containers to prevent exposure to air and moisture, which could affect its performance. Due to its controlled reactivity, it does not require extreme storage conditions, making it suitable for standard laboratory storage. Always handle with care, using appropriate personal protective equipment such as gloves and safety goggles. It is not classified as hazardous under standard laboratory conditions, but standard safety protocols should be followed to ensure safe handling and use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086240133338,"sku":"TCI2510C338518428","price":1818000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086240166106,"sku":"TCI2510C338518429","price":6310000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3385.jpg?v=1768204766"},{"product_id":"tci2510c343618472","title":"TCI C3436 1003845-08-6 2-Chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Chloro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrimidine is a chemical compound widely used in pharmaceutical research and development. It serves as a key building block in the synthesis of various pharmacologically active compounds. This reagent plays a crucial role in the creation of complex molecular structures, particularly in the field of drug discovery. Its unique chemical structure enables it to participate in multiple reaction types, making it an essential tool for researchers aiming to develop new therapeutic agents.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its chemical stability under controlled conditions and its ability to react with a variety of reagents, including amines, sulfides, and transition metals. Its versatility in participating in S-N coupling reactions and other nitrogen-sulfur bond-forming processes makes it a preferred choice for synthetic chemists. The presence of the boronic acid group enhances its reactivity and compatibility with various synthetic methodologies, supporting the development of bioactive molecules with specific therapeutic applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in research projects focused on drug development and pharmacological compound synthesis. Its availability in solid form and its ability to engage in chemical reactions make it a reliable and practical option for researchers. It is frequently employed in academic and industrial settings to explore new chemical pathways and improve the efficiency of drug discovery processes.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003ePharmaceutical Development: This compound is ideal for synthesizing complex drug molecules due to its reactivity and compatibility with various synthetic methods.\u003c\/li\u003e\n\u003cli\u003eDrug Discovery Research: It supports the creation of new therapeutic agents by participating in key chemical reactions that form nitrogen-sulfur bonds.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis Projects: Its stability and reactivity make it a valuable reagent in the preparation of bioactive compounds and molecular scaffolds.\u003c\/li\u003e\n\u003cli\u003eAcademic Research: It is widely used in university laboratories to study chemical reactions and develop new synthetic strategies for pharmaceutical applications.\u003c\/li\u003e\n\u003cli\u003eIndustrial R\u0026amp;D: It is employed in pharmaceutical companies to optimize synthetic routes and improve the efficiency of drug manufacturing processes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1003845-08-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Pharmaceutical Development and Drug Discovery Research Reagents \u0026gt; Building Blocks for Pharmaceutical Ingredients (for Research and Experimental Use)\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities suitable for laboratory use\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in airtight containers to prevent exposure to moisture and air. Due to its chemical reactivity, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. It is important to ensure that the storage area is well-ventilated to minimize the risk of inhalation of any vapors. Avoid contact with incompatible materials such as strong oxidizers or acids. Proper labeling and storage conditions are essential to ensure safe handling and long-term usability in laboratory settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086246359258,"sku":"TCI2510C343618472","price":1666000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086246392026,"sku":"TCI2510C343618473","price":5074000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3436.jpg?v=1767099581"},{"product_id":"tci2510c350018559","title":"TCI C3500 195062-61-4 2-(4-Chlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-(4-Chlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron compound widely used in organic chemistry laboratories. It serves as a key reagent in various synthetic processes, particularly in the construction of aromatic and heterocyclic compounds. This compound is a versatile tool in modern synthetic chemistry due to its ability to participate in multiple reaction pathways. Its role as a boronic acid derivative makes it especially valuable in cross-coupling reactions, where it facilitates the formation of carbon-carbon bonds with high efficiency and selectivity.\u003c\/p\u003e\n\u003cp\u003eThe compound's unique chemical structure and reactivity make it a preferred choice for chemists working in both academic and industrial settings. The presence of a chloro group on the aromatic ring enhances its reactivity and allows for targeted chemical transformations. Its stability under controlled conditions ensures reliable performance in laboratory experiments, while its reactivity enables the synthesis of complex molecular structures. These properties make it an essential component in the development of new pharmaceuticals and advanced materials.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic synthesis research, particularly in academic institutions and research centers. Its application spans across various fields, including pharmaceutical development, material science, and chemical engineering. Due to its reactivity and utility, it is frequently utilized in projects involving the synthesis of bioactive compounds and functional materials. Its presence in Indonesian laboratories underscores its importance in advancing chemical research and innovation.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003eSuzuki Coupling Reactions\u003c\/strong\u003e: This compound is ideal for Suzuki coupling due to its ability to form stable boronic acid derivatives, enabling efficient cross-coupling with aryl halides to create complex aromatic structures.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eKumada Coupling Reactions\u003c\/strong\u003e: It serves as a valuable reagent in Kumada coupling, where it facilitates the formation of carbon-carbon bonds through the use of organomagnesium reagents, enhancing synthetic versatility.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eSynthesis of Heterocyclic Compounds\u003c\/strong\u003e: Its reactivity allows for the selective formation of heterocyclic rings, making it a preferred choice in the synthesis of bioactive molecules and pharmaceutical intermediates.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eOrganic Synthesis Research\u003c\/strong\u003e: It is widely used in research settings to develop new synthetic methodologies and explore novel reaction mechanisms in organic chemistry.\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eMaterial Science Applications\u003c\/strong\u003e: Its ability to participate in cross-coupling reactions makes it useful in the synthesis of advanced materials, including polymers and functional coatings.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003e\n\u003cstrong\u003eBrand\u003c\/strong\u003e: TCI\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eCAS Number\u003c\/strong\u003e: 195062-61-4\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eCategory\u003c\/strong\u003e: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003ePack Sizes\u003c\/strong\u003e: Available in various quantities as per standard laboratory supply formats\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003ePhysical Form\u003c\/strong\u003e: Solid powder\u003c\/li\u003e\n\u003cli\u003e\n\u003cstrong\u003eStorage Note\u003c\/strong\u003e: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its stability and reactivity. It is recommended to use airtight containers to prevent exposure to moisture and air, which can affect its chemical integrity. As an organoboron compound, it is sensitive to moisture and should be handled with care to avoid unintended reactions. In laboratory settings, it is advisable to use gloves and appropriate personal protective equipment when handling this material. Proper labeling and storage conditions are essential to ensure safety and maintain the compound's effectiveness in chemical reactions. Always ensure that the storage area is well-ventilated and free from potential contaminants to preserve the compound's quality and performance.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086255829210,"sku":"TCI2510C350018559","price":1541000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086255861978,"sku":"TCI2510C350018560","price":5326000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3500-struktur.jpg?v=1791524965"},{"product_id":"tci2510c352918602","title":"TCI C3529 458532-84-8 2-Chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Chloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine is a highly reactive organoboron compound widely used in organic chemistry laboratories. It plays a crucial role in various synthetic processes, particularly in the formation of complex molecular structures. This compound is a key reagent in S-N coupling reactions, which are essential for the synthesis of heterocyclic compounds and other organic molecules. Its unique structure, featuring a boron-containing group, makes it a versatile tool for chemists seeking to build complex chemical frameworks.\u003c\/p\u003e\n\u003cp\u003eThe compound’s reactivity stems from its organoboron functionality, which allows it to participate in a wide range of chemical transformations. Its ability to react with amines, sulfides, and halides makes it particularly valuable in coupling reactions. The presence of the boron group enhances its compatibility with various synthetic strategies, enabling the creation of diverse chemical entities. This reactivity, however, also requires careful handling to ensure safety and efficiency in laboratory settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in the development of complex molecules. It is also employed in pharmaceutical and industrial chemical research due to its capacity to form compounds with specific structural features. Its application is widespread among researchers working on synthetic pathways that require precise chemical transformations. The compound’s utility in these contexts highlights its importance in modern chemical synthesis.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eS-N Coupling Reactions: This compound is ideal for S-N coupling due to its organoboron functionality, enabling the formation of complex heterocyclic structures.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis of Heterocycles: Its reactivity makes it a preferred reagent in the synthesis of various heterocyclic compounds, which are common in pharmaceuticals.\u003c\/li\u003e\n\u003cli\u003eIndustrial Chemical Production: The compound's ability to form specific molecular structures is valuable in the creation of specialized chemical products.\u003c\/li\u003e\n\u003cli\u003eResearch in Medicinal Chemistry: It is used to develop new drug compounds by facilitating the synthesis of complex organic molecules.\u003c\/li\u003e\n\u003cli\u003eAdvanced Organic Reaction Development: Its versatility supports the exploration of new synthetic methods in organic chemistry research.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 458532-84-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory reagent packaging\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the specific formulation and supplier packaging\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry place away from moisture and direct sunlight. It is recommended to use airtight containers made of materials compatible with organic solvents to prevent degradation. Due to its reactivity, it should be handled in a well-ventilated area, preferably under a fume hood, to minimize exposure. Proper personal protective equipment, such as gloves and safety goggles, should be worn during handling. The compound is not stable under prolonged exposure to air or light, so it should be used promptly after opening. Always follow standard laboratory safety protocols when working with reactive organoboron compounds.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086259892442,"sku":"TCI2510C352918602","price":1010000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086259925210,"sku":"TCI2510C352918603","price":3508000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3529.jpg?v=1769144276"},{"product_id":"tci2510c361218708","title":"TCI C3612 870195-94-1 2-(2-Chlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-(2-Chlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile organoboron compound widely used in organic synthesis, particularly in coupling reactions such as Suzuki and Kumada. This reagent plays a crucial role in the development of complex molecules by enabling the formation of carbon-carbon bonds under controlled conditions. Its unique structure, featuring a chloro group on the phenyl ring and a tetramethyl group on the dioxaborolan ring, makes it an essential component in the synthesis of heterocyclic compounds, pharmaceuticals, and industrial chemicals. In the laboratory, this compound is indispensable for reactions requiring high reactivity and specificity.\u003c\/p\u003e\n\u003cp\u003eThe compound's ability to coordinate with metals such as palladium makes it ideal for catalytic processes that require precise control over reaction mechanisms. Its reactivity is balanced by a degree of stability, allowing it to be used in a variety of reaction conditions, including low-temperature or anhydrous environments. This combination of reactivity and stability ensures that it remains a preferred choice for chemists working on challenging synthetic routes.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, particularly in academic and research institutions focused on the synthesis of complex molecules. Its application spans across both academic and industrial research, supporting the development of new drugs, materials, and chemical processes. The compound's reliability and effectiveness make it a staple in many laboratory settings.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its ability to form carbon-carbon bonds efficiently.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research for the development of new drug molecules requiring precise coupling reactions.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production where stable and reactive reagents are needed for complex syntheses.\u003c\/li\u003e\n\u003cli\u003eAcademic research in universities focusing on advanced organic chemistry techniques and methodologies.\u003c\/li\u003e\n\u003cli\u003eCatalytic processes involving palladium-based reactions that require organoboron reagents for enhanced efficiency.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 870195-94-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various sizes as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the specific formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry place, away from moisture and direct light to maintain its stability and reactivity. It is recommended to use airtight containers made of materials such as glass or polyethylene to prevent contamination and degradation. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment. In laboratory settings, it is important to ensure proper ventilation and avoid exposure to incompatible substances. Always follow standard safety protocols to minimize risks during handling and storage.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086270607578,"sku":"TCI2510C361218708","price":683000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086270640346,"sku":"TCI2510C361218709","price":2297000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3612.jpg?v=1769144263"},{"product_id":"tci2510c372118803","title":"TCI C3721 2507954-86-9 tert-Butyl 3-(4-Chlorobenzyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)azetidine-1-carboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTert-Butyl 3-(4-Chlorobenzyl)-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)azetidine-1-carboxylate is a complex organic compound used as a building block in chemical synthesis. This heterocyclic compound contains both an azetidine ring and a boronic acid group, making it a versatile reagent for various synthetic pathways. It is commonly employed in reactions that require specific chemical transformations, such as nucleophilic substitution and coupling reactions. Its structural complexity allows it to participate in advanced organic chemistry processes, supporting the development of new compounds with tailored properties.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical stability and reactivity make it a preferred choice for synthetic chemists. The presence of the boronic acid group enables it to undergo efficient coupling reactions, particularly in cross-coupling methodologies. Its compatibility with a range of solvents and reaction conditions enhances its utility in laboratory settings. Additionally, its ability to form stable intermediates under controlled conditions ensures reliable results in synthetic processes, making it a valuable tool in both academic and industrial research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is widely used in organic chemistry research, especially in the synthesis of heterocyclic compounds and drug development. Its unique structure and reactivity make it an essential component in studies focused on creating new pharmaceuticals and functional materials. Researchers rely on its predictable behavior and high reactivity to achieve precise chemical outcomes in their experiments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of heterocyclic compounds due to its azetidine and boronic acid groups enabling efficient coupling reactions.\u003c\/li\u003e\n\u003cli\u003eDrug development research as it supports the creation of complex molecular structures with pharmaceutical potential.\u003c\/li\u003e\n\u003cli\u003eNucleophilic substitution reactions where its stability and reactivity contribute to the formation of desired products.\u003c\/li\u003e\n\u003cli\u003eCross-coupling reactions benefiting from its compatibility with various reagents and reaction conditions.\u003c\/li\u003e\n\u003cli\u003eAdvanced chemical research in Indonesian laboratories focusing on new material synthesis and functional chemistry.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 2507954-86-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid depending on formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to moisture and air, which may affect its reactivity. Due to its potential chemical reactivity, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. Avoid contact with incompatible substances to ensure safe storage and use. In laboratory settings, it should be kept in a designated chemical storage area with proper labeling and access control. Regular monitoring of storage conditions ensures the compound remains in optimal condition for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48086279848154,"sku":"TCI2510C372118803","price":3811000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086279880922,"sku":"TCI2510C372118804","price":12164000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3721.jpg?v=1767099967"},{"product_id":"tci2510d249422736","title":"TCI D2494 68716-47-2 2,4-Dichlorophenylboronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,4-Dichlorophenylboronic Acid (TCI D2494) is a chemical compound widely used in organic reactions, particularly in the synthesis of boron-containing compounds. Its versatility makes it an essential reagent in modern chemical research, especially in the development of pharmaceuticals and organic materials. This compound is known for its ability to participate in various coupling reactions, such as the Suzuki-Miyaura reaction, which is crucial for the formation of complex organic structures and drug molecules. Its unique reactivity and compatibility with different ligands make it a valuable tool in molecular modification and functional group transformation.\u003c\/p\u003e\n\u003cp\u003eThe compound exhibits chemical stability under controlled conditions, though it is sensitive to moisture and oxidation. The presence of an anhydride in its composition enhances its stability during storage, although careful handling is still required. Its reactivity allows it to efficiently participate in complex chemical processes, making it a preferred choice for researchers aiming to achieve high yields and purity in their experiments. Its chemical properties and functional versatility make it a key component in many synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used by chemists and pharmacologists for the synthesis and characterization of new compounds. Its availability in various packaging options ensures ease of use and convenience for both academic and industrial research settings. The compound plays a significant role in advancing chemical innovation and pharmaceutical development in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eUsed in organic synthesis for the preparation of boronic acid derivatives, which are essential in the development of pharmaceutical compounds due to their reactivity and compatibility with various functional groups.\u003c\/li\u003e\n\u003cli\u003eApplied in Suzuki-Miyaura coupling reactions, which are widely used in the synthesis of heterocyclic compounds and pharmaceuticals, offering efficient and selective cross-coupling of aryl halides with boronic acids.\u003c\/li\u003e\n\u003cli\u003eEmployed in the modification of molecular structures through boron-based reactions, allowing for the introduction of functional groups and the creation of complex organic molecules with desired properties.\u003c\/li\u003e\n\u003cli\u003eUtilized in the synthesis of bioactive compounds, where its reactivity and stability contribute to the formation of compounds with therapeutic potential in drug discovery processes.\u003c\/li\u003e\n\u003cli\u003eIntegrated into research projects involving green chemistry, where its low toxicity and efficient reaction profiles support sustainable and environmentally friendly synthetic methods.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 68716-47-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various packaging options to suit different laboratory needs\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, typically in powder form\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry place away from moisture and oxidizing agents to maintain its stability and reactivity. It is recommended to use airtight containers made of materials such as glass or polyethylene to prevent exposure to humidity. Due to its sensitivity to oxidation, it is important to avoid prolonged exposure to air and light. Proper labeling and storage conditions are essential to ensure safety and maintain the compound's effectiveness. Laboratory personnel should wear appropriate personal protective equipment when handling this material to minimize any potential risks. Regular monitoring of storage conditions is advised to ensure the integrity of the compound throughout its shelf life.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086561882330,"sku":"TCI2510D249422736","price":481000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086561915098,"sku":"TCI2510D249422737","price":1389000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086561947866,"sku":"TCI2510D249422738","price":4366000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D2494.jpg?v=1769143952"},{"product_id":"tci2510d343523717","title":"TCI D3435 1133798-41-0 2,4,6-Tris(3,4-dichlorophenyl)boroxin","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,4,6-Tris(3,4-dichlorophenyl)boroxin is a highly reactive organoboron compound widely used in organic chemistry laboratories. It belongs to the category of organometallic reagents and is particularly valued for its ability to participate in various chemical reactions. This compound plays a crucial role in synthetic chemistry, especially in the development of complex molecular structures. Its unique chemical structure allows it to interact with a wide range of substrates, making it a versatile tool for researchers.\u003c\/p\u003e\n\u003cp\u003eThe compound's reactivity stems from its boroxin framework, which enables it to engage in both electrophilic and nucleophilic reactions. This characteristic makes it a preferred choice in laboratory settings where controlled chemical transformations are required. Its ability to form stable complexes with various ligands further enhances its utility in synthetic processes. Additionally, its stability under controlled conditions ensures reliable performance in experimental protocols.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2,4,6-Tris(3,4-dichlorophenyl)boroxin is commonly used by chemists for fundamental research and the development of new compounds. Its application spans across multiple areas of organic chemistry, including substitution reactions, coupling reactions, and the synthesis of heterocyclic compounds. Due to its reactivity and versatility, it remains a key reagent in the pursuit of advanced chemical synthesis and innovation.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSubstitution Reactions: This compound is ideal for substitution reactions due to its reactivity and ability to interact with various substrates.\u003c\/li\u003e\n\u003cli\u003eCoupling Reactions: Its organoboron structure makes it suitable for coupling reactions, facilitating the formation of complex molecular structures.\u003c\/li\u003e\n\u003cli\u003eHeterocyclic Compound Synthesis: The compound's unique chemical properties enable it to participate in the synthesis of heterocyclic compounds.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis Research: It is widely used in research settings for the development of new organic compounds and molecular structures.\u003c\/li\u003e\n\u003cli\u003eChemical Innovation Projects: Its versatility and reactivity make it a valuable tool in projects aimed at chemical innovation and discovery.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1133798-41-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the specific formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in airtight containers to prevent exposure to moisture and air. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment. Storage should be away from incompatible substances to avoid any potential chemical interactions. Regular monitoring of storage conditions is advised to ensure the integrity of the material. Proper labeling and safe handling practices are essential to maintain a safe laboratory environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086615490778,"sku":"TCI2510D343523717","price":1944000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086615523546,"sku":"TCI2510D343523718","price":5982000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3435.jpg?v=1768197249"},{"product_id":"tci2510d377224142","title":"TCI D3772 832114-00-8 3,5-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)isoxazole","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D3772, 3,5-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)isoxazole, CAS number 832114-00-8, is an organoboron reagent built on an isoxazole ring whose boron group is protected as a pinacol ester. The material is prepared specifically for cross-coupling reactions, particularly Suzuki–Miyaura couplings, in which the isoxazole heteroaromatic ring is joined to an aryl or heteroaryl halide. With a reagent of this kind, synthetic chemists can attach a dimethyl-substituted isoxazole fragment directly onto the framework of a target molecule, without having to construct that heterocyclic ring from scratch.\u003c\/p\u003e\n\u003cp\u003eThe advantage that makes this reagent a preferred choice lies in its pinacol ester form. Compared with free boronic acids, which tend to undergo deboronation readily and are difficult to weigh out consistently, pinacol esters are generally more stable in storage, easier to purify, and more robust during routine handling in the laboratory. The two methyl groups at the 3- and 5-positions provide steric protection and an electronic influence on the ring, while the isoxazole ring itself is a motif frequently encountered in bioactive molecules. That combination makes this reagent a practical option for expanding structural diversity.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, a reagent of this type is typically used in university and institutional synthetic chemistry groups, as well as in research units working on medicinal chemistry and heterocyclic building blocks. It is normally ordered in small quantities for specific coupling steps, weighed out on an analytical balance, and used in reactions run under an inert atmosphere with a palladium catalyst. Its stability as a pinacol ester is helpful in warm, humid conditions, where free boronic acids are less convenient to keep on the shelf.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSuzuki–Miyaura cross-coupling: the pinacol boronate transfers the isoxazole ring to aryl or heteroaryl halides under palladium catalysis, giving direct access to biaryl-type linkages.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry building block: the isoxazole ring is a motif often found in bioactive molecules, so this reagent installs a pharmacophore-relevant fragment in a single coupling step.\u003c\/li\u003e\n\u003cli\u003eHeteroaromatic fragment installation: instead of constructing the substituted isoxazole ring de novo, chemists can couple the ready-made 3,5-dimethylisoxazole unit straight onto an existing molecular framework.\u003c\/li\u003e\n\u003cli\u003eAnalogue synthesis and structural diversification: the reagent lets a research group vary the halide partner while keeping the isoxazole fragment constant, generating series of related compounds efficiently.\u003c\/li\u003e\n\u003cli\u003eMethod and catalyst screening: because pinacol esters are more stable and easier to weigh consistently than free boronic acids, this reagent gives reproducible input for optimising coupling conditions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eCAS number: 832114-00-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003eCatalogue number: D3772\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research-scale pack sizes; please confirm the currently listed options when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a tightly closed original container in a cool, dry place, away from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the reagent in its original tightly closed container in a cool, dry, well-ventilated place, protected from moisture and away from heat sources and direct sunlight. Amber glass or the supplied original packaging is suitable; for frequently opened stock, keeping the container in a desiccator or under an inert atmosphere helps preserve quality. Weigh out portions promptly and reseal the container to limit exposure to humid air. Handle in a fume hood using safety glasses, gloves, and a laboratory coat, avoid contact with skin, eyes, and clothing, and avoid breathing dust. Keep away from strong oxidising agents, label all derived solutions clearly, and dispose of residues and contaminated materials as chemical waste in accordance with institutional procedures. Always consult the manufacturer's safety data sheet before first use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086637084890,"sku":"TCI2510D377224142","price":1010000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086637117658,"sku":"TCI2510D377224143","price":3231000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3772.jpg?v=1769141913"},{"product_id":"tci2510d405724534","title":"TCI D4057 108847-20-7 Dibenzothiophene-4-boronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D4057 Dibenzothiophene-4-boronic Acid (CAS 108847-20-7) is an organoboron reagent that carries a boronic acid group at the 4-position of the dibenzothiophene framework. As is common for aromatic boronic acids, this product contains varying amounts of the boroxine anhydride formed by natural intermolecular dehydration. In synthetic laboratories, the compound serves as the nucleophilic partner in Suzuki-Miyaura cross-coupling reactions, the most reliable method for forming carbon-carbon bonds between two aromatic fragments. With this reagent, a dibenzothiophene unit can be attached directly and efficiently onto a target molecular scaffold.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this reagent widely chosen is the character of the dibenzothiophene unit itself. Its rigid, electron-rich tricyclic framework provides high thermal stability, a large triplet energy, and good hole-transporting behaviour, which is why it has become a favoured motif in the design of organic light-emitting diode materials. The 4-position, located adjacent to the sulfur atom, gives a distinctive substitution geometry that influences molecular shape and solid-state packing. It should be noted that the presence of the anhydride causes the effective molecular weight to vary, so stoichiometric calculations should account for this.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used in university and institutional research groups working on organic synthesis, functional materials, and optoelectronics, as well as in industrial R\u0026amp;D units developing new molecular scaffolds. It is normally handled in gram or sub-gram quantities on the bench, weighed out for coupling reactions under inert atmosphere, and stored alongside other moisture-sensitive organometallic reagents in a controlled chemical store.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSuzuki-Miyaura cross-coupling: acts as the nucleophilic boron partner that transfers the dibenzothiophene fragment to an aryl halide, forming a robust biaryl carbon-carbon bond under palladium catalysis.\u003c\/li\u003e\n\u003cli\u003eOLED material synthesis: introduces a dibenzothiophene unit whose high triplet energy and thermal stability make it a preferred building block for host and charge-transport materials.\u003c\/li\u003e\n\u003cli\u003eHole-transport layer development: the electron-rich tricyclic core imparts good hole-transporting character, so the reagent is useful when constructing molecules intended for hole-transporting functions.\u003c\/li\u003e\n\u003cli\u003eFunctional aromatic scaffold construction: allows direct, efficient attachment of a rigid sulfur-containing tricycle onto larger conjugated frameworks without multi-step protection or functional group manipulation.\u003c\/li\u003e\n\u003cli\u003eStructure-property studies: substitution at the 4-position adjacent to sulfur gives distinctive geometry, letting researchers examine how substitution pattern affects molecular shape and solid-state packing.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 108847-20-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003eComposition note: contains varying amounts of the corresponding boroxine anhydride\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI catalogue pack sizes; please confirm the required size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage note: keep tightly closed in a cool, dry place, protected from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the reagent in its original tightly closed container in a cool, dry, well-ventilated chemical store, away from moisture and sources of ignition. Aromatic boronic acids absorb water and undergo further dehydration to the boroxine on standing, so the container should be closed promptly after each use and, where practicable, kept under an inert atmosphere. Weigh the solid in a fume hood using clean, dry spatulas and glassware. Wear a laboratory coat, safety glasses, and chemically resistant gloves. Because the anhydride content varies, verify stoichiometry before use and consult the manufacturer's safety data sheet for full handling guidance.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086653501658,"sku":"TCI2510D405724534","price":1491000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086653534426,"sku":"TCI2510D405724535","price":4771000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4057.jpg?v=1769141943"},{"product_id":"tci2510d420124726","title":"TCI D4201 1003298-87-0 2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D4201, 2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol with CAS number 1003298-87-0, is an organoboron reagent belonging to the organometallic reagent family. Its molecular structure consists of a phenol ring carrying two chlorine atoms at the positions ortho to the hydroxyl group, together with a pinacol boronate ester group at the para position. This combination of three distinct functional groups on a single aromatic core makes the compound a highly useful starting material in modern organic synthesis, particularly in cross-coupling reactions that require both a boron partner and an additional handle for further functionalization within the same molecule.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes this reagent a preferred choice among researchers is the stability of the pinacol boronate ester, which is considerably easier to handle, weigh, and store than the corresponding free boronic acid, since free boronic acids tend to form cyclic anhydrides and complicate accurate stoichiometric determination. The phenolic hydroxyl group provides a site for etherification, esterification, or directed hydrogen bonding, while the two ortho chlorine atoms exert an electronic effect that lowers the electron density of the ring and at the same time introduce a distinctive steric environment. Together, these features allow researchers to design synthetic strategies around a single, well-defined building block.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is typically used in university research groups, government research institutes, and industrial R\u0026amp;D units engaged in synthetic organic chemistry and medicinal chemistry programmes. It is commonly employed at the bench scale within multi-step synthesis campaigns, where a reliable and reproducible boron coupling partner is needed. Because the pinacol ester form is straightforward to weigh out and store under ordinary laboratory conditions, it fits well into teaching and research workflows that depend on consistent, well-characterised commercial reagents.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSuzuki-Miyaura cross-coupling reactions: the pinacol boronate ester acts as a stable and reliable boron partner for forming carbon-carbon bonds with aryl halides and related electrophiles under palladium catalysis.\u003c\/li\u003e\n\u003cli\u003eMedicinal chemistry building block synthesis: the three independent functional groups allow chemists to assemble substituted biaryl scaffolds and elaborate them further without needing to introduce additional handles at a later stage.\u003c\/li\u003e\n\u003cli\u003eSequential functionalization strategies: after the boronate has been consumed in coupling, the phenolic hydroxyl group remains available for etherification or esterification, enabling a controlled, stepwise construction of complex targets.\u003c\/li\u003e\n\u003cli\u003eMaterials and ligand precursor preparation: the electron-poor dichlorophenol ring provides a distinctive electronic profile that is useful when preparing aromatic frameworks and coordinating motifs for functional material studies.\u003c\/li\u003e\n\u003cli\u003eMethod development and reaction screening: the well-defined, easily weighed solid form supports accurate stoichiometry, making it suitable for optimising catalyst systems, solvents, and bases in coupling methodology studies.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 1003298-87-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003eChemical name: 2,6-Dichloro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research-scale packaging; please confirm the currently offered pack size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: store in a tightly closed container in a cool, dry place away from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the reagent in a tightly closed original container in a cool, dry, and well-ventilated area, protected from moisture and direct sunlight, since boronate esters are sensitive to prolonged exposure to humid air. Use amber or opaque chemically resistant containers where extended storage is required, and keep the container closed when not in active use. Handle the material inside a fume hood, wearing safety goggles, chemical-resistant gloves, and a laboratory coat. Weigh the solid carefully to avoid dust formation, and always consult the manufacturer's safety data sheet before use, disposal, or transfer between containers.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086678307034,"sku":"TCI2510D420124726","price":2828000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086678339802,"sku":"TCI2510D420124727","price":13527000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4201.jpg?v=1768205031"},{"product_id":"tci2510d435724932","title":"TCI D4357 185990-03-8 2-(Dimethylphenylsilyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-(Dimethylphenylsilyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a synthetic reagent widely used in organic chemistry for the formation of C-X (non-halogen) bonds. This compound plays a crucial role in laboratory settings where complex molecular structures need to be synthesized with high precision. Its unique chemical structure enables it to participate in various reaction mechanisms, making it an essential tool for chemists working on advanced synthetic pathways. It is particularly valuable in applications that require controlled reactivity and compatibility with a wide range of substrates.\u003c\/p\u003e\n\u003cp\u003eThe compound's stability under specific conditions, combined with its reactivity in targeted chemical environments, makes it a preferred choice in modern synthetic chemistry. Its molecular framework, containing both boron and silicon atoms, provides versatility in reaction types such as coupling and substitution. These properties allow it to be used in a variety of synthetic strategies, including those involving boron-based reagents. Its ability to maintain structural integrity during synthesis processes ensures consistent results, which is vital for research and development in chemical laboratories.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is commonly used in organic chemistry research, especially in academic and research institutions. It supports the development of new synthetic techniques and contributes to the advancement of chemical knowledge. Its application in molecular modification and complex compound synthesis makes it a key component in the toolkit of chemists working on innovative projects. The compound's relevance in both educational and industrial research contexts underscores its importance in the chemical sciences.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from this reagent's ability to form stable C-X bonds, enabling the creation of complex molecular structures with high efficiency.\u003c\/li\u003e\n\u003cli\u003eBoron-based reaction systems often require reagents with specific reactivity profiles, and this compound provides the necessary chemical versatility for such processes.\u003c\/li\u003e\n\u003cli\u003eMolecular modification projects rely on its capacity to undergo substitution and coupling reactions, making it ideal for functional group transformations.\u003c\/li\u003e\n\u003cli\u003eResearch in synthetic chemistry frequently involves the use of non-halogen bond-forming agents, and this compound is a reliable choice for such investigations.\u003c\/li\u003e\n\u003cli\u003eAdvanced chemical synthesis in Indonesian laboratories utilizes this reagent to develop new methodologies and improve existing synthetic routes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 185990-03-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Synthetic Reagents \u0026gt; C-X(Non-Halogen) Bond Formation [Synthetic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard supplier offerings\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on the specific formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and air exposure, which can affect its reactivity. In laboratory settings, it should be handled with appropriate personal protective equipment to ensure safety. Due to its chemical nature, it should be stored separately from incompatible substances to avoid potential reactions. Regular monitoring of storage conditions is advised to ensure optimal performance and safety in laboratory applications. Proper labeling and storage practices are essential to maintain the integrity of the compound and ensure safe handling in research environments.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086688465114,"sku":"TCI2510D435724932","price":1818000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086688497882,"sku":"TCI2510D435724933","price":5856000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4357.jpg?v=1769141984"},{"product_id":"tci2510d437324951","title":"TCI D4373 668983-97-9 Dibenzothiophene-2-boronic Acid (contains varying amounts of Anhydride)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eDibenzothiophene-2-boronic Acid is a chemical compound widely used in organic reactions, particularly in the synthesis of heterocyclic compounds and coupling reactions. As an organoboron reagent, it plays a crucial role in modern synthetic chemistry, enabling the formation of complex molecular structures. This compound is commonly found in chemical and pharmaceutical laboratories due to its ability to react with various functional groups, such as halides, amines, and hydroxyls. Its versatility makes it an essential tool for researchers working on advanced organic synthesis.\u003c\/p\u003e\n\u003cp\u003eThe compound exhibits stable chemical properties under specific conditions, although it can react with acidic or basic substances. The presence of varying amounts of anhydride in the compound influences its reactivity, necessitating careful handling. It dissolves well in organic solvents such as ethyl acetate and ethanol, which facilitates its use in laboratory processes. These characteristics make it a preferred choice for applications requiring controlled reactivity and solubility.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Dibenzothiophene-2-boronic Acid is frequently used in organic chemistry research, especially in the development of pharmaceutical compounds and industrial chemicals. Its availability and effectiveness have made it a valuable reagent for both academic and industrial research. Due to its specialized nature, it is often sought after for advanced synthetic projects in the chemical sector.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eUsed in Suzuki-Miyaura coupling reactions due to its reactivity with aryl halides, enabling efficient cross-coupling in organic synthesis.\u003c\/li\u003e\n\u003cli\u003eApplied in Kumada-Corriu reactions for the formation of carbon-carbon bonds, facilitating the synthesis of complex organic molecules.\u003c\/li\u003e\n\u003cli\u003eEmployed in the synthesis of heterocyclic compounds, where its ability to react with functional groups is essential for structural modifications.\u003c\/li\u003e\n\u003cli\u003eUtilized in pharmaceutical research for the development of new drug compounds, as it contributes to the formation of key molecular frameworks.\u003c\/li\u003e\n\u003cli\u003eIntegrated into industrial chemical processes for the production of specialty chemicals, where controlled reactivity and solubility are critical.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 668983-97-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or powder, depending on the batch and supplier\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eDibenzothiophene-2-boronic Acid should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to moisture and air, which can affect its reactivity. Due to its potential to react with acidic or basic substances, it should be handled with care, using appropriate personal protective equipment such as gloves and goggles. It is best stored in a well-ventilated laboratory area to minimize any risk of inhalation. Avoid contact with incompatible materials to ensure safe handling and long-term stability. Proper storage conditions help preserve the compound’s effectiveness for use in various laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086689218778,"sku":"TCI2510D437324951","price":758000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086689251546,"sku":"TCI2510D437324952","price":2297000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4373-struktur.jpg?v=1791525009"}],"url":"https:\/\/amiscientific.com\/en\/collections\/tci-l3-organoboron-organometallic-reagents.oembed?page=20","provider":"AMI Scientific","version":"1.0","type":"link"}