{"title":"Boronic Acids and Derivatives [Organoboron]","description":"\u003cp\u003eBoronic Acids and Derivatives [Organoboron] — reagen TCI untuk riset dan industri. Tersedia di Indonesia melalui AMI Scientific.\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\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eTCI B5580 merupakan reagen organoboron berbasis fluorena yang berfungsi sebagai building block penting dalam sintesis organik, khususnya pada reaksi kopling silang Suzuki-Miyaura. Senyawa ini mengandung gugus dioxaborolane yang reaktif serta substituen bromo pada posisi 7 dari kerangka fluorena, menjadikannya prekursor serbaguna untuk konstruksi molekul kompleks berbasis fluorena tersubstitusi.\u003c\/p\u003e\n\u003cp\u003eSenyawa ini banyak diaplikasikan dalam pengembangan material organik fungsional, seperti Organic Light-Emitting Diodes (OLED), sel surya organik (organic photovoltaics), dan semikonduktor organik. Selain itu, turunan fluorena yang dihasilkan dari reagen ini juga digunakan dalam riset sensor fluoresen, polimer konjugasi, serta material elektroaktif untuk perangkat elektronik dan optoelektronik.\u003c\/p\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek\/Vendor: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 620624-96-6\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003eVarian\/Kemasan: 200 mg\u003c\/li\u003e\n\u003cli\u003eCatatan: Simpan pada suhu dingin (refrigerator), dalam wadah tertutup rapat, terlindung dari cahaya dan kelembaban; tangani dalam lemari asam karena bersifat iritan pada kulit, mata, dan saluran pernapasan\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eEnglish\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":3908000.0,"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\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eN-(tert-Butoxycarbonyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline merupakan reagen organoboron serbaguna yang berfungsi sebagai building block penting dalam sintesis organik, khususnya untuk reaksi kopling silang Suzuki-Miyaura. Senyawa ini memiliki gugus boronat pinakol ester pada posisi para dari cincin anilin, sekaligus dilindungi oleh gugus tert-butoxycarbonyl (Boc) pada fungsi amina, sehingga memberikan selektivitas dan kestabilan tinggi selama proses sintesis bertahap.\u003c\/p\u003e\n\u003cp\u003eReagen ini banyak diaplikasikan dalam riset kimia medisinal dan pengembangan obat untuk mensintesis senyawa biaril tersubstitusi amina, yang merupakan kerangka struktural penting pada berbagai kandidat farmasi. Selain itu, senyawa ini juga digunakan dalam sintesis material fungsional, ligan, serta intermediat kimia halus yang memerlukan gugus anilin terlindungi untuk modifikasi lebih lanjut.\u003c\/p\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 330793-01-6\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003eVarian Kemasan: 1g, 5g\u003c\/li\u003e\n\u003cli\u003ePenyimpanan: Simpan dalam wadah tertutup rapat pada suhu dingin (disarankan refrigerator), hindari paparan kelembapan dan cahaya langsung\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eEnglish\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":1153000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085889384666,"sku":"TCI2510B558812257","price":3964000.0,"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\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eTCI B5656 adalah reagen organoboron berbasis spirobifluorene yang berfungsi sebagai building block serbaguna dalam sintesis organik lanjutan. Senyawa ini mengandung dua gugus boronat ester (pinacol ester) pada posisi 2 dan 7 dari kerangka spirobifluorene, menjadikannya prekursor ideal untuk reaksi kopling silang Suzuki-Miyaura. Laboratorium penelitian kimia material banyak mengandalkan senyawa ini untuk membangun polimer terkonjugasi dan material molekuler dengan kemurnian tinggi.\u003c\/p\u003e\n\u003cp\u003eAplikasi utamanya mencakup fabrikasi material Organic Light-Emitting Diode (OLED), sensor fluoresensi, dan semikonduktor organik. Kerangka spirobifluorene yang kaku dan ortogonal memberikan stabilitas termal serta mencegah agregasi molekuler yang tidak diinginkan, sehingga material yang dihasilkan memiliki efisiensi emisi cahaya yang unggul. Senyawa ini juga digunakan dalam pengembangan porous organic polymers dan covalent organic frameworks (COF).\u003c\/p\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek\/Vendor: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 728911-52-2\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron\u003c\/li\u003e\n\u003cli\u003eVarian\/Kemasan: 1 g\u003c\/li\u003e\n\u003cli\u003eCatatan: Simpan di tempat sejuk dan kering, terlindung dari kelembapan; senyawa organoboron dapat terhidrolisis jika terpapar udara lembap dalam waktu lama\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eEnglish\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":3993000.0,"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\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003e2,2'-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,1'-biphenyl merupakan reagen organoboron bifungsional yang banyak digunakan dalam reaksi kopling silang Suzuki-Miyaura untuk membangun ikatan biaril secara efisien. Senyawa ini berperan sebagai donor boron ganda yang memungkinkan konstruksi rantai polimer terkonjugasi dan kerangka molekul kompleks dalam satu tahap sintesis.\u003c\/p\u003e\n\u003cp\u003eSenyawa ini umum diaplikasikan dalam sintesis bahan organik fungsional seperti OLED, sensor fluoresensi, serta material semikonduktor organik. Selain itu, reagen ini juga dimanfaatkan dalam pengembangan senyawa farmasi dan agrokimia yang memerlukan struktur bifenil tersubstitusi sebagai inti aktifnya.\u003c\/p\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI\u003c\/li\u003e\n\u003cli\u003eNomor Katalog: B5703\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 398128-09-1\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron\u003c\/li\u003e\n\u003cli\u003eVarian Kemasan: 200 mg, 1 g\u003c\/li\u003e\n\u003cli\u003eSimpan dalam kondisi kering dan sejuk, hindari paparan kelembapan berlebih untuk menjaga stabilitas gugus boronat ester.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eEnglish\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":2166000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085898199258,"sku":"TCI2510B570312417","price":7478000.0,"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\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003e3,3'-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,1'-biphenyl adalah reagen organoboron bifungsional yang banyak digunakan dalam reaksi kopling silang Suzuki-Miyaura, khususnya untuk sintesis polimer konjugatif dan kerangka organik berbasis bifenil. Senyawa ini berperan sebagai building block penting karena memiliki dua gugus boronat ester yang reaktif pada posisi meta, memungkinkan pembentukan ikatan karbon-karbon secara selektif dengan berbagai aril halida.\u003c\/p\u003e\n\u003cp\u003eDi laboratorium, reagen ini umum diaplikasikan dalam sintesis material fungsional seperti covalent organic frameworks (COFs), metal-organic frameworks (MOFs), dan polimer konduktif yang memerlukan unit penghubung bifenil kaku. Selain itu, senyawa ini juga dimanfaatkan dalam pengembangan sensor kimia, material optoelektronik, serta sebagai prekursor untuk ligan dalam katalisis homogen.\u003c\/p\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 850264-92-5\u003c\/li\u003e\n\u003cli\u003eKode Produk: B5704\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron\u003c\/li\u003e\n\u003cli\u003eVarian\/Kemasan: 200 mg dan 1 g\u003c\/li\u003e\n\u003cli\u003eSimpan di tempat sejuk dan kering, wadah tertutup rapat, serta terlindung dari kelembapan untuk mencegah hidrolisis gugus boronat ester.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eEnglish\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":1857000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085898264794,"sku":"TCI2510B570412419","price":6409000.0,"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\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eTCI B5770 adalah reagen organoboron berbasis dioxaborolane yang dirancang untuk reaksi kopling silang, khususnya pada sintesis senyawa aromatik kompleks. Senyawa ini mengandung gugus bifenil dan antrasena yang membuatnya ideal sebagai prekursor dalam pembentukan ikatan karbon-karbon melalui reaksi Suzuki-Miyaura, salah satu metode paling andal dalam kimia organik sintetik modern.\u003c\/p\u003e\n\u003cp\u003eReagen ini umum digunakan dalam pengembangan material optoelektronik, seperti organic light-emitting diode (OLED) dan semikonduktor organik, karena kerangka antrasena yang dimilikinya memiliki sifat fluoresensi yang unggul. Selain itu, senyawa ini juga diaplikasikan dalam riset farmasi untuk membangun perpustakaan molekul aromatik tersubstitusi yang berpotensi sebagai kandidat obat baru.\u003c\/p\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek\/Vendor: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 1416243-42-9\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003eVarian\/Kemasan: 1g\u003c\/li\u003e\n\u003cli\u003ePenyimpanan: Simpan pada suhu ruang, dalam wadah tertutup rapat, terlindung dari kelembapan dan cahaya langsung.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eEnglish\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":4105000.0,"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\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eTCI B5774 adalah pereaksi organoboron berbasis bis(pinacolatoboron) yang terikat pada kerangka nafto-bisoksadiazol, menjadikannya senyawa kunci untuk reaksi kopling silang Suzuki-Miyaura di laboratorium sintesis organik. Senyawa ini dirancang sebagai building block dwifungsi yang memungkinkan konstruksi polimer konjugasi dan material molekuler berbasis heterosiklik secara presisi.\u003c\/p\u003e\n\u003cp\u003eDi ranah riset, senyawa ini banyak dimanfaatkan dalam pengembangan material optoelektronik seperti Organic Light-Emitting Diodes (OLED), sel surya organik (OPV), dan sensor fluoresensi berkat sifat akseptor elektron dari unit oksadiazol. Selain itu, senyawa ini juga relevan untuk studi kimia material supramolekul dan sintesis ligan berstruktur rigid.\u003c\/p\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek\/Vendor: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eNomor CAS: Tidak tercantum dalam data\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003eVarian\/Kemasan: 100 mg\u003c\/li\u003e\n\u003cli\u003ePenyimpanan: Simpan di tempat kering dan sejuk, hindari paparan kelembapan berlebih untuk menjaga stabilitas gugus boronat ester\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eEnglish\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":10877000.0,"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\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003e2-(Benzo[b]thiophen-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane merupakan reagen organoboron berbentuk ester pinakol dari benzotiofena yang umum digunakan sebagai building block dalam reaksi kopling silang Suzuki-Miyaura. Senyawa ini berfungsi sebagai donor gugus aril heterosiklik yang memungkinkan pembentukan ikatan karbon-karbon antara cincin benzotiofena dengan berbagai substrat aril halida atau triflat.\u003c\/p\u003e\n\u003cp\u003eAplikasi utama reagen ini mencakup sintesis senyawa heterosiklik kompleks untuk riset farmasi, pengembangan material optoelektronik berbasis tiofena, serta preparasi ligan dan katalis organologam. Benzotiofena tersubstitusi yang dihasilkan dari reagen ini banyak dijumpai sebagai kerangka inti dalam molekul kandidat obat dengan aktivitas biologis beragam.\u003c\/p\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 171364-86-6\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron\u003c\/li\u003e\n\u003cli\u003eVarian\/kemasan: 1 g\u003c\/li\u003e\n\u003cli\u003eSimpan dalam kondisi sejuk dan kering, wadah tertutup rapat, serta terlindung dari kelembapan untuk menjaga stabilitas ester boronat\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eEnglish\u003c\/h3\u003e\n\u003cp\u003eTCI B5821 2-(Benzo[b]thiophen-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS 171364-86-6) is a benzothiophene-derived pinacol boronic ester widely employed as a coupling partner in Suzuki-Miyaura cross-coupling reactions. This organoboron reagent enables the introduction of the benzo[b]thiophene heterocyclic moiety into diverse molecular scaffolds, making it valuable in medicinal chemistry, materials science, and ligand synthesis. Packaged in a 1 g quantity, this reagent is suitable for small-scale exploratory synthesis and reaction optimization studies in research laboratories.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085905047770,"sku":"TCI2510B582112570","price":4470000.0,"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\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003e2-(Benzofuran-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane adalah reagen organoboron dengan gugus benzofuran yang berfungsi sebagai prekursor serbaguna dalam reaksi kopling silang Suzuki-Miyaura. Senyawa ini memungkinkan peneliti untuk memperkenalkan unit benzofuran ke dalam kerangka molekul target secara efisien dan selektif. Dengan kemurnian tinggi standar TCI, reagen ini sangat andal untuk sintesis organik di laboratorium penelitian maupun industri.\u003c\/p\u003e\n\u003cp\u003eSenyawa boronat ester ini banyak diaplikasikan dalam pengembangan kandidat obat dan material fungsional, mengingat benzofuran merupakan inti heterosiklik yang lazim ditemukan pada senyawa bioaktif. Di laboratorium kimia medisinal, reagen ini digunakan untuk membangun pustaka senyawa turunan benzofuran dengan beragam substitusi. Selain itu, senyawa ini juga bermanfaat dalam sintesis material organik seperti polimer terkonjugasi dan senyawa optoelektronik.\u003c\/p\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 519054-55-8\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron\u003c\/li\u003e\n\u003cli\u003eVarian Kemasan: 250 mg, 1 g\u003c\/li\u003e\n\u003cli\u003eSimpan di tempat sejuk dan kering, terlindung dari cahaya dan kelembapan; kemasan dijaga tetap tertutup rapat saat tidak digunakan\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eEnglish\u003c\/h3\u003e\n\u003cp\u003e2-(Benzofuran-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a benzofuran-substituted boronate ester designed for Suzuki-Miyaura cross-coupling reactions, enabling the efficient introduction of the benzofuran moiety into target molecular scaffolds. This organoboron reagent is widely utilized in medicinal chemistry for the synthesis of benzofuran-based compound libraries and drug candidate development. It also finds application in materials science for constructing conjugated polymers and optoelectronic materials.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48085905178842,"sku":"TCI2510B582312573","price":1378000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085905211610,"sku":"TCI2510B582312574","price":4077000.0,"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\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003e1-(tert-Butoxycarbonyl)-1,2,5,6-tetrahydro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine merupakan reagen organoboron berkualitas tinggi dari TCI yang berfungsi sebagai intermediate penting dalam sintesis organik, khususnya pada reaksi kopling silang Suzuki-Miyaura. Senyawa ini dilengkapi gugus pelindung Boc (tert-butoxycarbonyl) pada cincin tetrahidropiridin serta gugus boronat pinakol ester yang reaktif, menjadikannya building block serbaguna untuk konstruksi ikatan karbon-karbon.\u003c\/p\u003e\n\u003cp\u003eSenyawa ini umum digunakan dalam riset kimia medisinal dan pengembangan farmasi untuk sintesis molekul heterosiklik kompleks, terutama derivat piridin tersubstitusi yang banyak ditemukan pada kandidat obat. Selain itu, reagen ini juga diaplikasikan dalam sintesis bahan aktif farmasi (API), pengembangan agrokimia, serta penelitian material fungsional berbasis senyawa heteroaromatik.\u003c\/p\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 885693-20-9\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003eVarian Kemasan: 200 mg, 1 g\u003c\/li\u003e\n\u003cli\u003ePenyimpanan: Simpan dalam wadah tertutup rapat di tempat sejuk dan kering, hindari paparan kelembapan dan cahaya langsung\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eEnglish\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":1266000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085906292954,"sku":"TCI2510B584412604","price":4049000.0,"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\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003e2,5-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thiophene merupakan reagen organoboron bifungsional berbasis tiofena yang banyak digunakan dalam reaksi kopling silang, khususnya kopling Suzuki-Miyaura. Senyawa ini berperan sebagai building block penting untuk memperkenalkan unit tiofena ke dalam kerangka molekul organik melalui pembentukan ikatan karbon-karbon yang efisien dengan adanya katalis paladium.\u003c\/p\u003e\n\u003cp\u003eDi laboratorium riset, reagen ini umum diaplikasikan dalam sintesis polimer konjugasi, material semikonduktor organik, dan senyawa heterosiklik untuk pengembangan sel surya organik (organic photovoltaics), OLED, serta sensor kimia berbasis tiofena. Selain itu, senyawa ini juga dimanfaatkan dalam sintesis farmasi dan agrokimia untuk membangun struktur molekul kompleks yang mengandung cincin tiofena tersubstitusi.\u003c\/p\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 175361-81-6\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron\u003c\/li\u003e\n\u003cli\u003eVarian\/Kemasan: Tersedia dalam ukuran 1g dan 5g\u003c\/li\u003e\n\u003cli\u003ePenyimpanan: Simpan pada suhu rendah (refrigerator) dalam wadah tertutup rapat, terlindung dari cahaya dan kelembapan\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eEnglish\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":1687000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085907374298,"sku":"TCI2510B587112632","price":6016000.0,"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\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eSenyawa 2-(3-Buten-1-il)-4,4,5,5-tetrametil-1,3,2-dioksaborolana merupakan reagen organoboron serbaguna yang banyak digunakan dalam reaksi kopling silang, khususnya reaksi Suzuki-Miyaura. Produk ini distabilkan dengan phenothiazine untuk mencegah degradasi selama penyimpanan dan menjaga kemurnian tinggi dalam aplikasi sintesis organik.\u003c\/p\u003e\n\u003cp\u003eReagen ini berperan sebagai prekursor boronat ester yang dapat bereaksi dengan berbagai elektrofil untuk membentuk ikatan karbon-karbon baru. Aplikasi utamanya meliputi sintesis senyawa farmasi, pengembangan material fungsional, serta penelitian kimia medisinal yang memerlukan gugus alkenil sebagai building block.\u003c\/p\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 331958-92-0\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron\u003c\/li\u003e\n\u003cli\u003eVarian kemasan: 1g dan 5g\u003c\/li\u003e\n\u003cli\u003eCatatan: Distabilkan dengan Phenothiazine; simpan dalam wadah tertutup rapat pada suhu ruang, hindari kelembapan\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eEnglish\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":2531000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085911929050,"sku":"TCI2510B596012740","price":8966000.0,"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\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eN,N'-Bis(2-ethylhexyl)-6,6'-bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)isoindigo merupakan reagen organoboron berbasis isoindigo yang berfungsi sebagai building block penting dalam sintesis organik. Senyawa ini mengandung dua gugus pinacol boronate ester yang siap digunakan dalam reaksi cross-coupling, khususnya reaksi Suzuki-Miyaura, untuk membangun ikatan karbon-karbon pada kerangka molekul kompleks.\u003c\/p\u003e\n\u003cp\u003eSenyawa ini banyak diaplikasikan dalam pengembangan material semikonduktor organik, terutama untuk fabrikasi organic field-effect transistors (OFETs) dan organic photovoltaics (OPVs). Struktur isoindigo yang bersifat electron-deficient menjadikannya kandidat unggul sebagai akseptor elektron dalam polimer donor-akseptor untuk divais elektronik fleksibel.\u003c\/p\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 1821433-54-8\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron\u003c\/li\u003e\n\u003cli\u003eVarian\/Kemasan: 200 mg\u003c\/li\u003e\n\u003cli\u003eSimpan pada suhu dingin (2–8°C), dalam wadah tertutup rapat, serta terlindung dari kelembapan dan cahaya langsung.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eEnglish\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":6184000.0,"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\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eTCI B5994 merupakan reagen organoboron bifungsional berbasis isoindigo yang dirancang sebagai blok penyusun (building block) untuk sintesis polimer terkonjugasi dan molekul kecil dalam riset material organik. Senyawa ini memiliki dua gugus pinakol boronat ester yang reaktif dalam reaksi kopling silang Suzuki-Miyaura, memungkinkan polimerisasi terarah dengan unit donor-akseptor lainnya. Kehadiran rantai alkil bercabang 2-oktildodesil pada atom nitrogen memberikan kelarutan tinggi pada produk polimer yang dihasilkan, sebuah karakteristik penting untuk pemrosesan larutan dalam fabrikasi perangkat.\u003c\/p\u003e\n\u003cp\u003eSenyawa ini umum diaplikasikan dalam pengembangan material semikonduktor organik untuk transistor efek medan organik (OFET) dan sel surya organik (OPV). Unit isoindigo yang kekurangan elektron menjadikannya akseptor yang sangat baik dalam arsitektur polimer donor-akseptor, menghasilkan celah pita sempit yang menguntungkan untuk penyerapan cahaya tampak hingga inframerah dekat. Peneliti di bidang elektronik organik, sensor, dan perangkat optoelektronik sering menggunakan monomer ini untuk mengeksplorasi polimer konjugasi baru dengan mobilitas muatan tinggi dan efisiensi konversi energi yang optimal.\u003c\/p\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 1563062-80-5\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron\u003c\/li\u003e\n\u003cli\u003eVarian\/Kemasan: 200mg\u003c\/li\u003e\n\u003cli\u003eSimpan di tempat sejuk dan kering, sebaiknya dalam atmosfer inert serta terlindung dari cahaya dan kelembapan\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eEnglish\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":5791000.0,"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\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003e2,5-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 merupakan senyawa organoboron berbasis inti diketopyrrolopyrrole (DPP) yang difungsionalisasi dengan gugus ester boronat pada rantai tiofena. Senyawa ini berperan sebagai building block penting dalam sintesis material semikonduktor organik melalui reaksi kopling silang, khususnya kopling Suzuki-Miyaura, untuk menghasilkan polimer konjugasi dengan sifat elektronik yang dapat disetel.\u003c\/p\u003e\n\u003cp\u003eSenyawa ini banyak diaplikasikan dalam riset pengembangan perangkat elektronik organik seperti sel surya organik (OPV), transistor efek medan organik (OFET), dan dioda pemancar cahaya organik (OLED). Kehadiran rantai alkil bercabang 2-decyltetradecyl memberikan kelarutan tinggi dalam pelarut organik umum, sehingga memudahkan pemrosesan larutan dan fabrikasi film tipis untuk karakterisasi perangkat.\u003c\/p\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eNomor Katalog: B5996\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 1412448-63-5\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron\u003c\/li\u003e\n\u003cli\u003eKemasan: 200 mg\u003c\/li\u003e\n\u003cli\u003eSimpan pada suhu dingin (refrigerator), dalam wadah tertutup rapat, terlindung dari cahaya dan kelembapan\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eEnglish\u003c\/h3\u003e\n\u003cp\u003eTCI B5996 is a diketopyrrolopyrrole (DPP)-based organoboron compound featuring boronic ester groups on thiophene side chains, designed as a versatile building block for Suzuki-Miyaura cross-coupling reactions in conjugated polymer synthesis. Its branched 2-decyltetradecyl alkyl chains impart excellent solubility in common organic solvents, facilitating solution-processed device fabrication. This reagent is widely utilized in research on organic photovoltaics (OPV), organic field-effect transistors (OFET), and related optoelectronic applications requiring high-purity organometallic precursors.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085913796826,"sku":"TCI2510B599612780","price":8152000.0,"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\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eTCI B6006 1,6-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrene merupakan reagen organoboron bifungsional berbasis pirena yang berperan sebagai building block penting dalam sintesis organik. Senyawa ini mengandung dua gugus boronat ester pada posisi 1 dan 6 cincin pirena, menjadikannya sangat reaktif dalam reaksi kopling silang Suzuki-Miyaura untuk membangun sistem aromatik polisiklik yang lebih kompleks.\u003c\/p\u003e\n\u003cp\u003eDi laboratorium, reagen ini banyak diaplikasikan dalam sintesis material organik fungsional seperti Organic Light-Emitting Diodes (OLED), sensor fluoresen, dan Metal-Organic Frameworks (MOF) berbasis pirena. Selain itu, senyawa ini juga digunakan dalam pengembangan konduktor organik, semikonduktor molekuler, serta studi fotofisika karena sifat fluoresensi intrinsik inti pirenanya yang tinggi.\u003c\/p\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 950779-13-2\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003eVarian\/Kemasan: 1 g, 5 g\u003c\/li\u003e\n\u003cli\u003eSimpan di tempat sejuk dan kering, hindari paparan kelembapan berlebih; wadah harus selalu tertutup rapat setelah digunakan.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eEnglish\u003c\/h3\u003e\n\u003cp\u003eTCI B6006 1,6-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrene is a bifunctional organoboron reagent featuring two pinacol boronate ester groups attached to a pyrene core, making it an excellent cross-coupling partner for Suzuki-Miyaura reactions. This compound serves as a key building block in the construction of extended π-conjugated systems for advanced functional materials, including OLED emitters, fluorescent sensors, and porous organic frameworks. Its pyrene backbone also imparts strong fluorescence properties, enabling applications in molecular electronics and photophysical investigations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085914386650,"sku":"TCI2510B600612794","price":4975000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085914419418,"sku":"TCI2510B600612795","price":16808000.0,"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\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eTCI B6023 2-([1,1'-Biphenyl]-3-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane merupakan reagen organoboron berupa pinacol ester dari asam 3-bifenilboronat yang dirancang untuk reaksi kopling Suzuki-Miyaura. Senyawa ini menyediakan gugus bifenil dalam bentuk boronat yang stabil dan siap digunakan untuk membentuk ikatan karbon-karbon (C–C) dengan berbagai aril halida atau pseudohalida di laboratorium sintesis organik.\u003c\/p\u003e\n\u003cp\u003eReagen ini banyak diaplikasikan dalam pengembangan senyawa farmasi, material organik fungsional, serta riset kimia medicinal yang memerlukan kerangka bifenil pada struktur molekul target. Kestabilan gugus pinacol ester-nya menjadikan reagen ini mudah ditangani dan disimpan dibandingkan asam boronat bebas yang lebih rentan terhadap kelembaban.\u003c\/p\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 912844-88-3\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003eVarian kemasan: 1 g, 5 g\u003c\/li\u003e\n\u003cli\u003ePenyimpanan: Simpan dalam wadah tertutup rapat di tempat sejuk dan kering, terlindung dari kelembaban dan cahaya langsung\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eEnglish\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":816000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085915369690,"sku":"TCI2510B602312819","price":2559000.0,"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\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003e2-(3-Bromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane adalah reagen organoboron berupa ester pinakol dari asam 3-bromofenilboronat. Senyawa ini berperan penting sebagai building block dalam reaksi kopling Suzuki-Miyaura untuk membentuk ikatan karbon-karbon antara fragmen aromatik dengan berbagai elektrofil organik.\u003c\/p\u003e\n\u003cp\u003eSenyawa ini banyak diaplikasikan dalam sintesis obat-obatan, pengembangan bahan agrokimia, dan riset material organik. Selain reaksi Suzuki, ester boronat ini juga dapat dimanfaatkan dalam reaksi Petasis, homologasi Matteson, serta sebagai prekursor untuk konversi gugus fungsi lainnya dalam jalur sintesis kimia organik.\u003c\/p\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek\/Vendor: TCI\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 594823-67-3\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron\u003c\/li\u003e\n\u003cli\u003eVarian Kemasan: 1 g, 5 g\u003c\/li\u003e\n\u003cli\u003eSimpan pada suhu dingin (refrigerator), wadah tertutup rapat, serta terlindung dari kelembapan dan cahaya langsung\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eEnglish\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":844000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085915467994,"sku":"TCI2510B602412821","price":2559000.0,"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\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003e1-(tert-Butoxycarbonyl)-3,5-dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrazole merupakan reagen organoboron fungsional yang dirancang sebagai building block dalam sintesis organik lanjutan, khususnya pada reaksi kopling silang Suzuki-Miyaura. Senyawa ini menggabungkan gugus pinakol boronat ester dengan cincin pirazol tersubstitusi yang dilindungi gugus Boc, sehingga memungkinkan pembentukan ikatan karbon-karbon secara selektif pada posisi C-4 pirazol.\u003c\/p\u003e\n\u003cp\u003eAplikasi umum reagen ini mencakup sintesis kandidat obat berbasis pirazol, pengembangan bahan agrokimia, serta konstruksi ligan dan material fungsional. Keberadaan gugus pelindung Boc memudahkan deproteksi dan fungsionalisasi lebih lanjut, menjadikannya prekursor serbaguna dalam riset kimia medisinal dan penemuan senyawa bioaktif.\u003c\/p\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eNomor Katalog: B6026\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 1073354-70-7\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron\u003c\/li\u003e\n\u003cli\u003eKemasan Tersedia: 200 mg, 1 g\u003c\/li\u003e\n\u003cli\u003eSimpan pada suhu 2–8 °C, dalam wadah tertutup rapat, terlindung dari kelembapan dan cahaya langsung.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eEnglish\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 versatile organoboron reagent designed for Suzuki-Miyaura cross-coupling reactions. The pinacol boronate ester moiety enables selective C–C bond formation at the pyrazole C-4 position, while the Boc protecting group allows straightforward subsequent deprotection and derivatization. This compound is widely used in medicinal chemistry for constructing pyrazole-based drug candidates, as well as in agrochemical and materials research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085915631834,"sku":"TCI2510B602612824","price":1294000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085915664602,"sku":"TCI2510B602612825","price":4442000.0,"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\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eTCI B6050 1,4-Benzenediboronic Acid Bis(neopentyl Glycol) Ester merupakan reagen organoboron berkualitas tinggi yang berfungsi sebagai prekursor serbaguna dalam reaksi kopling silang Suzuki-Miyaura. Senyawa ini memiliki dua gugus boron ester yang terlindungi oleh neopentyl glycol, membuatnya lebih stabil terhadap oksidasi dan hidrolisis dibandingkan asam boronat bebas, sekaligus tetap reaktif dalam kondisi reaksi yang sesuai. Struktur 1,4-disubstitusi pada cincin benzena memungkinkan pembentukan ikatan karbon-karbon di dua posisi secara simultan atau bertahap.\u003c\/p\u003e\n\u003cp\u003eReagen ini banyak diaplikasikan dalam sintesis senyawa bifenil tersubstitusi, polimer konjugasi, serta kerangka metal-organik (MOF) dan covalent organic frameworks (COF). Dalam riset kimia material, senyawa ini digunakan untuk membangun struktur molekul linier dengan presisi tinggi. Selain itu, reagen ini juga bermanfaat dalam sintesis intermediat farmasi dan pengembangan material optoelektronik.\u003c\/p\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 5565-36-6\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron\u003c\/li\u003e\n\u003cli\u003eVarian\/Kemasan: 1 g\u003c\/li\u003e\n\u003cli\u003eCatatan: Simpan di tempat sejuk dan kering, hindari paparan kelembapan berlebih untuk menjaga stabilitas ester boronat\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eEnglish\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":2194000.0,"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\u003eDeskripsi\u003c\/h3\u003e\n\u003cp\u003eTCI B6552 adalah 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], sebuah senyawa spiro terkonjugasi yang membawa dua gugus ester boronat pinakol pada posisi 2' dan 7'. Rangka spiro yang menyatukan unit fluorena dengan unit cyclopenta-dipiridina memberikan struktur tiga dimensi yang kaku dan tegak lurus, arsitektur yang banyak dicari dalam desain material fungsional. Kehadiran atom nitrogen piridinik pada salah satu sisi rangka menjadikan molekul ini tidak sekadar kerangka hidrokarbon, melainkan juga kandidat ligan pendonor nitrogen. Kombinasi tersebut menempatkannya pada kategori Nitrogen-Donor Ligands dalam katalog TCI.\u003c\/p\u003e\n\u003cp\u003eDua gugus pinacol boronate pada molekul ini berfungsi sebagai titik sambung yang sangat andal untuk reaksi kopling silang terkatalisis paladium, terutama kopling Suzuki–Miyaura. Sifat difungsional tersebut memungkinkan senyawa dipakai sebagai monomer inti dalam pembentukan oligomer maupun polimer terkonjugasi, atau sebagai pusat percabangan untuk molekul besar berbentuk bintang. Dibandingkan asam boronat bebas, bentuk ester pinakol umumnya lebih mudah ditangani dan dimurnikan melalui kromatografi. Hal ini memberi keleluasaan bagi peneliti yang membangun pustaka material secara bertahap.\u003c\/p\u003e\n\u003cp\u003eDi laboratorium riset material organik, senyawa dengan pola spiro seperti ini menarik karena mampu menekan agregasi antarmolekul dan menjaga sifat pembentukan lapisan tipis yang baik. Unit dipiridina yang miskin elektron dapat dipadukan dengan segmen kaya elektron untuk menyusun sistem donor–akseptor. AMI Scientific menyediakan produk ini dalam kemasan kecil yang sesuai untuk tahap penapisan sintesis dan optimasi kondisi reaksi. Setiap detail struktur dan data analitik sebaiknya dirujuk pada dokumen resmi TCI yang menyertai produk.\u003c\/p\u003e\n\u003ch3\u003eAplikasi Laboratorium\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eKopling Suzuki–Miyaura — dua gugus boronat pinakol menjadikannya monomer difungsional yang siap disambungkan dengan aril halida.\u003c\/li\u003e\n\u003cli\u003eSintesis polimer terkonjugasi — rangka spiro kaku membantu menghasilkan rantai dengan kelarutan dan morfologi lapisan yang terkendali.\u003c\/li\u003e\n\u003cli\u003eRiset material OLED dan optoelektronik organik — arsitektur spirobifluorena banyak dipelajari sebagai kerangka host maupun pemancar.\u003c\/li\u003e\n\u003cli\u003eDesain ligan pendonor nitrogen — atom nitrogen piridinik dapat berkoordinasi dengan pusat logam transisi untuk kajian katalisis.\u003c\/li\u003e\n\u003cli\u003eKonstruksi molekul donor–akseptor — segmen dipiridina yang miskin elektron cocok dipasangkan dengan blok kaya elektron.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpesifikasi\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMerek: TCI\u003c\/li\u003e\n\u003cli\u003eNomor CAS: 2763205-15-6\u003c\/li\u003e\n\u003cli\u003eKategori: Chemistry \u0026gt; Catalysis and Inorganic Chemistry \u0026gt; Nitrogen-Donor Ligands [Catalysis]\u003c\/li\u003e\n\u003cli\u003eVarian\/kemasan: 100 mg dan 500 mg\u003c\/li\u003e\n\u003cli\u003eBentuk fisik: padatan organik; rujuk label dan lembar data resmi TCI untuk deskripsi rinci\u003c\/li\u003e\n\u003cli\u003ePenyimpanan: tempat sejuk, kering, dan terlindung cahaya, sesuai anjuran pada kemasan\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003ePenanganan dan Penyimpanan\u003c\/h3\u003e\n\u003cp\u003eTangani senyawa ini di dalam lemari asam menggunakan sarung tangan, kacamata pelindung, dan jas laboratorium. Ester boronat sebaiknya dijauhkan dari kelembapan berlebih dan wadah ditutup rapat setiap selesai digunakan, karena paparan uap air dapat memengaruhi kualitas bahan. Ikuti seluruh anjuran penyimpanan dan pembuangan limbah yang tercantum pada lembar data keselamatan resmi produk.\u003c\/p\u003e\n\u003ch3\u003eEnglish\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":2194000.0,"currency_code":"IDR","in_stock":true},{"title":"500mg","offer_id":48085946892506,"sku":"TCI2510B655213481","price":7618000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6552.jpg?v=1767093890"},{"product_id":"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":4414000.0,"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":1266000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086100902106,"sku":"TCI2510C206616717","price":3880000.0,"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":760000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086143205594,"sku":"TCI2510C262117448","price":2559000.0,"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 organic chemistry for its unique reactivity and versatility. This reagent plays a critical role in various synthetic processes, particularly in the formation of complex organic molecules. Its ability to participate in coupling reactions, such as the Suzuki-Miyaura reaction, makes it an essential component in the development of pharmaceuticals and advanced materials. Due to its structural complexity, it offers precise control over reaction outcomes, enhancing the efficiency of laboratory workflows.\u003c\/p\u003e\n\u003cp\u003eThe compound's organoboron structure provides high reactivity under specific conditions, making it a preferred choice for chemists working on intricate synthesis pathways. Its stability in controlled environments ensures consistent performance, while its reactivity with transition metals enables the synthesis of a wide range of compounds. The presence of cyclohexene in its molecular framework adds to its reactivity, allowing for the creation of diverse chemical structures. These properties make it a reliable and powerful tool in modern organic synthesis.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in research focused on organic chemistry, particularly in the synthesis of pharmaceutical compounds and new materials. Its high reactivity and specificity make it ideal for applications requiring precise chemical transformations. Researchers in Indonesia rely on this reagent for its ability to facilitate complex reactions, supporting advancements in both academic and industrial chemical research.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis for the creation of heterocyclic and aromatic compounds due to its reactivity and coupling capabilities.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research for the development of new drug molecules through efficient synthetic pathways.\u003c\/li\u003e\n\u003cli\u003eMaterial science applications in the production of advanced polymers and functional materials.\u003c\/li\u003e\n\u003cli\u003eCatalytic reactions involving transition metals, where its organoboron structure enhances reaction efficiency.\u003c\/li\u003e\n\u003cli\u003eSynthetic chemistry projects requiring precise control over reaction outcomes and molecular structure formation.\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: 141091-37-4\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, away from moisture and direct sunlight to maintain its chemical stability. It is recommended to use airtight containers made of glass or polyethylene to prevent contamination and degradation. 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 exposure to incompatible substances, and always follow standard laboratory safety protocols to minimize risks associated with its use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086192718042,"sku":"TCI2510C270717558","price":2840000.0,"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":1210000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086198419674,"sku":"TCI2510C282317697","price":4582000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C2823.jpg?v=1768204704"},{"product_id":"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":816000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086206513370,"sku":"TCI2510C299317907","price":2475000.0,"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":1462000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086214017242,"sku":"TCI2510C310118059","price":5032000.0,"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":816000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086215033050,"sku":"TCI2510C312618086","price":3092000.0,"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":2362000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086221947098,"sku":"TCI2510C324318236","price":8180000.0,"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":1097000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086230663386,"sku":"TCI2510C330118322","price":3824000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3301.jpg?v=1768204758"},{"product_id":"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":844000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086238527706,"sku":"TCI2510C336718409","price":2671000.0,"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":2025000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086240166106,"sku":"TCI2510C338518429","price":7027000.0,"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":1857000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086246392026,"sku":"TCI2510C343618473","price":5651000.0,"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":1715000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086255861978,"sku":"TCI2510C350018560","price":5932000.0,"currency_code":"IDR","in_stock":true}]},{"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":1125000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086259925210,"sku":"TCI2510C352918603","price":3908000.0,"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":760000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086270640346,"sku":"TCI2510C361218709","price":2559000.0,"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. 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