{"title":"Fluorenes, Fluorenones [Small Molecule Semiconductor Building Blocks]","description":"\u003cp\u003e\u003cstrong\u003eFluorenes, Fluorenones [Small Molecule Semiconductor Building Blocks]\u003c\/strong\u003e — mencakup kerangka fluorena dan fluorenon terhalogenasi maupun tersubstitusi gugus boronat, amina, atau aril, yang berfungsi sebagai unit penyusun molekul semikonduktor organik. Struktur planar terkonjugasi pada inti fluorena memberi sifat elektronik dan optik yang dapat disetel lewat substitusi.\u003c\/p\u003e\u003cp\u003eFluorenes dan Fluorenones dipakai peneliti material organik dalam sintesis senyawa untuk OLED, transistor organik, dan sel surya organik melalui reaksi kopling seperti Suzuki atau Buchwald-Hartwig. Turunan terbrominasi atau teriodinasi berperan sebagai titik awal fungsionalisasi, sedangkan turunan boronat langsung dipakai sebagai mitra kopling dalam pembangunan struktur oligomer dan polimer terkonjugasi.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510i079336057\"\u003eTCI I0793 2523-42-4 2-Iodofluorene\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b552112171\"\u003eTCI B5521 4269-17-4 4-Bromo-9H-fluoren-9-one\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510i087536166\"\u003eTCI I0875 144981-85-1 2-Iodo-9,9-dimethylfluorene\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b558012243\"\u003eTCI B5580 620624-96-6 2-(7-Bromo-9,9-di-n-octyl-9H-fluoren-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t391655629\"\u003eTCI T3916 171408-77-8 2,2',7-Tribromo-9,9'-spirobi[fluorene]\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b558112244\"\u003eTCI B5581 1196107-75-1 2-Bromo-13,13-dimethyl-6,11-di(naphthalen-2-yl)-13H-indeno[1,2-b]anthracene\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t380755499\"\u003eTCI T3807 1372778-68-1 N-([1,1':3',1''-Terphenyl]-5'-yl)-9,9-dimethyl-9H-fluoren-2-amine\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b561612303\"\u003eTCI B5616 1257251-75-4 9-(3-Bromophenyl)-9-phenyl-9H-fluorene\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan posisi dan jenis halogen atau gugus boronat pada cincin aromatik, tingkat kemurnian untuk aplikasi elektronik, serta kelarutan pada pelarut organik yang dipakai dalam proses sintesis. Seluruh produk merupakan produk asli Tokyo Chemical Industry (TCI) Jepang, dengan kemurnian, kemasan, dan kondisi penyimpanan tercantum pada halaman masing-masing item.\u003c\/p\u003e\u003cp\u003eKategori lain yang sejajar di bawah Small Molecule Semiconductor Building Blocks, sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-carbazoles-small-molecule-semiconductor-building-blocks\"\u003eCarbazoles [Small Molecule Semiconductor Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-thiophenes-small-molecule-semiconductor-building-blocks\"\u003eThiophenes [Small Molecule Semiconductor Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-anthracenes-anthraquinones-small-molecule-semiconductor-building-blocks\"\u003eAnthracenes, Anthraquinones [Small Molecule Semiconductor Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-small-molecule-semiconductor-building-blocks-others\"\u003eSmall Molecule Semiconductor Building Blocks (Others)\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-secondary-arylamines-small-molecule-semiconductor-building-blocks\"\u003eSecondary Arylamines [Small Molecule Semiconductor Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-benzothiophenes-small-molecule-semiconductor-building-blocks\"\u003eBenzothiophenes [Small Molecule Semiconductor Building Blocks]\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l3-small-molecule-semiconductor-building-blocks\"\u003eSmall Molecule Semiconductor Building Blocks\u003c\/a\u003e. Untuk pengadaan volume besar, kemasan khusus, atau grade tertentu, hubungi tim AMI Scientific — distributor resmi TCI Japan di Indonesia — untuk pengecekan ketersediaan dan lead time langsung ke Jepang.\u003c\/p\u003e","products":[{"product_id":"tci2510b552112171","title":"TCI B5521 4269-17-4 4-Bromo-9H-fluoren-9-one","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e4-Bromo-9H-fluoren-9-one (CAS 4269-17-4) is a brominated fluorenone derivative that serves as a versatile intermediate in organic synthesis, particularly for cross-coupling reactions. It is widely used as a building block in the preparation of pharmaceuticals, dyes, and functional materials. This product is suitable for organic chemistry research and material science applications in academic and industrial laboratories.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085885124826,"sku":"TCI2510B552112171","price":2699000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5521.jpg?v=1767092457"},{"product_id":"tci2510b558012243","title":"TCI B5580 620624-96-6 2-(7-Bromo-9,9-di-n-octyl-9H-fluoren-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5580 is an organoboron reagent featuring a 9,9-di-n-octylfluorene core with a bromo substituent at the 7-position and a reactive dioxaborolane group, serving as a versatile building block for Suzuki-Miyaura cross-coupling reactions. This compound is widely employed in the synthesis of functional organic materials, including OLED emitters, organic photovoltaics, and conjugated polymers for optoelectronic applications. Its well-defined structure and reliable reactivity make it a valuable precursor for constructing fluorene-based molecular architectures in academic and industrial research settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085887975642,"sku":"TCI2510B558012243","price":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":"tci2510b561712305","title":"TCI B5617 117766-40-2 9,9-Bis(4-methoxyphenyl)-9H-fluorene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5617 9,9-Bis(4-methoxyphenyl)-9H-fluorene (CAS 117766-40-2) is a high-purity small molecule semiconductor building block designed for advanced materials research. This fluorene-based compound serves as a key precursor for synthesizing hole-transporting layers, host materials, and conjugated polymers in organic electronics. It is widely applied in the development of OLEDs, organic photovoltaics, perovskite solar cells, and organic field-effect transistors (OFETs).\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085891317978,"sku":"TCI2510B561712305","price":2419000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085891350746,"sku":"TCI2510B561712306","price":8320000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5617.jpg?v=1768815838"},{"product_id":"tci2510b565612352","title":"TCI B5656 728911-52-2 2,7-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9,9'-spirobi[9H-fluorene]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5656 (CAS 728911-52-2) is a spirobifluorene-based organoboron reagent featuring two pinacol boronate ester groups, making it an excellent building block for Suzuki-Miyaura cross-coupling reactions. Its rigid, orthogonal spirobifluorene core imparts high thermal stability and effectively suppresses intermolecular aggregation, which is highly desirable in organic optoelectronic applications. This compound is widely employed in the synthesis of OLED materials, fluorescent sensors, organic semiconductors, and porous organic frameworks.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085894299866,"sku":"TCI2510B565612352","price":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":"tci2510b567312376","title":"TCI B5673 2041-19-2 3-Bromo-9H-fluoren-9-one","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5673 3-Bromo-9H-fluoren-9-one (CAS 2041-19-2) is a brominated fluorenone derivative widely utilized as a non-heterocyclic building block in organic synthesis laboratories. Its reactive bromo substituent at the 3-position makes it an excellent substrate for cross-coupling reactions, including Suzuki, Heck, and Sonogashira couplings, enabling the construction of complex molecular architectures. This compound is particularly valuable in research involving optoelectronic materials, OLED development, organic semiconductors, and pharmaceutical intermediate synthesis.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085895250138,"sku":"TCI2510B567312376","price":4442000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5673.jpg?v=1767092651"},{"product_id":"tci2510b567812382","title":"TCI B5678 736928-22-6 2-Bromo-9-phenyl-9H-fluoren-9-ol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Bromo-9-phenyl-9H-fluoren-9-ol is a non-heterocyclic building block featuring a substituted fluorene core with a reactive bromo group and a tertiary hydroxyl group. This compound serves as a versatile precursor in cross-coupling reactions and structural elaboration for advanced organic synthesis. It is commonly employed in the development of functional organic materials, fluorescent compounds, and as an intermediate in pharmaceutical research and medicinal chemistry.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085895577818,"sku":"TCI2510B567812382","price":1827000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5678.jpg?v=1768815858"},{"product_id":"tci2510b584212599","title":"TCI B5842 899422-06-1 2-Bromospiro[9H-fluorene-9,9'-[9H]xanthene]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Bromospiro[9H-fluorene-9,9'-[9H]xanthene] is a heterocyclic building block featuring a distinctive spiro architecture that combines fluorene and xanthene frameworks. This compound serves as a versatile precursor in advanced organic synthesis, particularly for constructing complex spiro-based molecules for materials science applications such as OLEDs and organic semiconductors. Its rigid spiro structure also makes it a valuable scaffold in chiral ligand design and heterocyclic drug discovery research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48276770750682,"sku":"TCI2510B584212599","price":1322000.0,"currency_code":"IDR","in_stock":false}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5842_e2ad23d0-bb0e-4716-9985-8039749f6ec4.jpg?v=1767863565"},{"product_id":"tci2510b612812947","title":"TCI B6128 1609484-45-8 4-Bromospiro[fluorene-9,9'-xanthene]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6128 4-Bromospiro[fluorene-9,9'-xanthene] (CAS 1609484-45-8) is a heterocyclic building block featuring a rigid spirocyclic framework, widely employed in advanced organic synthesis. It serves as a key precursor for constructing functional organic materials, particularly in the development of OLED emitters and organic photovoltaic devices. Its unique spiro structure suppresses intermolecular aggregation, making it valuable for optoelectronic and materials science research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085921202394,"sku":"TCI2510B612812947","price":1885000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085921235162,"sku":"TCI2510B612812948","price":6718000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6128_fe88d307-c572-4814-af85-1f0a974fa6c3.jpg?v=1767864632"},{"product_id":"tci2510b618013007","title":"TCI B6180 6051-98-5 7H-Benzo[c]fluoren-7-one","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e7H-Benzo[c]fluoren-7-one (CAS 6051-98-5) is a polycyclic aromatic ketone widely employed as a non-heterocyclic building block in advanced organic synthesis. Its highly conjugated structure makes it suitable for materials science research, particularly in the development of organic electronic devices such as OLEDs and organic semiconductors. This compound is also utilized in the design of fluorescent probes and photochemical studies across academic and industrial laboratories.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085923627226,"sku":"TCI2510B618013007","price":4526000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6180.jpg?v=1767093271"},{"product_id":"tci2510b622313051","title":"TCI B6223 182121-12-6 9,9-Bis(methoxymethyl)-9H-fluorene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e9,9-Bis(methoxymethyl)-9H-fluorene (CAS 182121-12-6, TCI B6223) is a non-heterocyclic building block primarily used as a versatile precursor in organic synthesis for constructing substituted fluorene frameworks. It is widely applied in the development of conjugated polymers, electroluminescent materials for OLED devices, and organometallic chemistry. Its dual methoxymethyl groups at the 9-position offer excellent reactivity for further functionalization in advanced material science and sensor research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085925200090,"sku":"TCI2510B622313051","price":1434000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085925232858,"sku":"TCI2510B622313052","price":5032000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6223.jpg?v=1768816008"},{"product_id":"tci2510b698113857","title":"TCI B6981 2192306-77-5 9-Bromospiro[benzo[c]fluorene-7,9'-xanthene]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6981 9-Bromospiro[benzo[c]fluorene-7,9'-xanthene] (CAS 2192306-77-5) is a spiro-configured heterocyclic building block combining a benzofluorene unit with a xanthene moiety. The orthogonal spiro geometry restricts molecular aggregation and supports amorphous film formation, a property widely exploited in organic electronic materials research. Its aryl bromide handle allows straightforward elaboration through Suzuki–Miyaura coupling and Buchwald–Hartwig amination. AMI Scientific supplies this building block in 200 mg and 1 g pack sizes for synthetic and materials laboratories.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085963210970,"sku":"TCI2510B698113857","price":1603000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085963243738,"sku":"TCI2510B698113858","price":5509000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6981.jpg?v=1767094456"},{"product_id":"tci2510c354318627","title":"TCI C3543 1459162-69-6 2-Chloro-4,6-bis(9,9-dimethyl-9H-fluoren-2-yl)-1,3,5-triazine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Chloro-4,6-bis(9,9-dimethyl-9H-fluoren-2-yl)-1,3,5-triazine is a complex organic compound widely used in laboratory settings for its versatility in chemical synthesis. As a heterocyclic building block, it plays a crucial role in the development of new materials and compounds with specific functional properties. Its unique molecular structure allows for the incorporation of various functional groups, making it an essential tool for researchers working in organic chemistry and material science. This compound is particularly valuable for its ability to participate in a range of chemical reactions, enabling the synthesis of compounds with tailored optical and electronic properties.\u003c\/p\u003e\n\u003cp\u003eThe compound's stability and reactivity make it a preferred choice for advanced chemical research. Its molecular structure includes both chloro and fluorene groups, which contribute to its chemical stability and optical properties. These characteristics allow it to be used in applications requiring precise control over molecular behavior, such as in the development of fluorescent materials or electronic components. The compound's ability to interact with multiple functional groups further enhances its utility in the synthesis of complex molecules. Its chemical inertness under controlled conditions also ensures reliable performance in laboratory experiments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in research related to organic chemistry, material science, and optical technologies. It is a key component in the development of new materials with specific functional properties, such as fluorescence or conductivity. Many research institutions and universities in Indonesia utilize this compound for both fundamental research and applied projects, contributing to advancements in scientific innovation and industrial applications.\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 stable intermediates and participate in various reaction pathways.\u003c\/li\u003e\n\u003cli\u003eMaterial science research uses it to develop fluorescent materials and electronic components due to its optical and chemical properties.\u003c\/li\u003e\n\u003cli\u003eOptical technology development leverages its fluorescence characteristics for creating advanced light-emitting materials.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research may utilize its structure for designing compounds with specific biological activities and reactivity.\u003c\/li\u003e\n\u003cli\u003eIndustrial applications in chemical manufacturing benefit from its role as a versatile building block for complex molecule synthesis.\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: 1459162-69-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical stability. It is recommended to use airtight containers made of glass or high-density polyethylene to prevent contamination and degradation. Due to its chemical nature, it should be handled with appropriate personal protective equipment, including gloves and safety goggles, to ensure laboratory safety. Avoid exposure to heat or open flames, as it may react under extreme conditions. Regular monitoring of storage conditions is advised to ensure the compound remains in optimal condition for use in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086261760218,"sku":"TCI2510C354318627","price":3401000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086261792986,"sku":"TCI2510C354318628","price":11777000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C3543.jpg?v=1767099746"},{"product_id":"tci2510d168521550","title":"TCI D1685 42523-29-5 2,7-Dihydroxy-9H-fluoren-9-one","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,7-Dihydroxy-9H-fluoren-9-one is a chemical compound widely used in organic reactions for the synthesis of complex molecules. As a building block, it plays a crucial role in the development of new compounds by offering versatile functional group compatibility. Its aromatic structure provides stability, making it a reliable choice for various chemical processes. This compound is particularly valuable in laboratories where the synthesis of heterocyclic and aromatic derivatives is required.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical and physical properties are consistent, ensuring predictable behavior in different experimental conditions. Its reactivity allows it to participate in substitution and oxidation reactions, making it suitable for a wide range of applications. The stability of its molecular structure ensures that it maintains its integrity during chemical transformations, which is essential for accurate and reproducible results.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2,7-Dihydroxy-9H-fluoren-9-one is commonly used in chemical, pharmaceutical, and materials research. It is a key component in the development of new drugs and the study of specific chemical properties. Its availability in the local market makes it accessible to researchers and students, supporting both academic and industrial applications.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSynthesis of heterocyclic compounds for pharmaceutical development due to its versatile functional group compatibility and stable aromatic structure.\u003c\/li\u003e\n\u003cli\u003eAromatic substitution reactions in organic chemistry research because of its reactivity and predictable chemical behavior.\u003c\/li\u003e\n\u003cli\u003eDevelopment of new materials in chemical research due to its ability to participate in various chemical transformations.\u003c\/li\u003e\n\u003cli\u003eStudy of chemical properties in academic institutions for educational and experimental purposes.\u003c\/li\u003e\n\u003cli\u003eDrug discovery applications in pharmaceutical laboratories for the synthesis of complex molecular structures.\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: 42523-29-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and sources of heat. It is recommended to use airtight containers to prevent moisture absorption and contamination. Due to its chemical stability, it does not require refrigeration but should be kept in a secure location to avoid accidental exposure. In laboratory settings, it is important to handle the compound with care, using appropriate personal protective equipment such as gloves and safety goggles. Proper labeling of containers is essential to ensure safe handling and prevent mix-ups with other chemicals. Always follow standard safety protocols when working with organic compounds to maintain a safe and controlled environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086455845082,"sku":"TCI2510D168521550","price":1603000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086455877850,"sku":"TCI2510D168521551","price":5509000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D1685.jpg?v=1769144052"},{"product_id":"tci2510d323523485","title":"TCI D3235 4569-45-3 9,9-Dimethylfluorene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e9,9-Dimethylfluorene is an organic compound widely used in scientific research, particularly in the field of materials science. It serves as a fundamental building block for the development of advanced materials, including semiconductors and optical components. Its unique molecular structure allows for modifications that can yield compounds with tailored optical and electronic properties, making it a versatile tool in modern laboratory settings. This compound is essential for researchers aiming to create new materials with specific functionalities and performance characteristics.\u003c\/p\u003e\n\u003cp\u003eThe compound is prized for its chemical stability and controlled reactivity, which make it suitable for high-precision applications. Its complex molecular structure remains manageable under laboratory conditions, allowing for efficient processing and manipulation. Additionally, its colorless nature and relatively high melting point facilitate separation and purification processes. These properties contribute to its reliability and effectiveness in various experimental setups. The ability of 9,9-Dimethylfluorene to form bonds with different functional groups enhances its flexibility in chemical modifications and molecular synthesis, making it a preferred choice for researchers.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 9,9-Dimethylfluorene is commonly used in material science and chemical research. It supports studies related to semiconductor development, optical material synthesis, and advanced chemical engineering. Its application is widespread in academic and industrial research settings, where it plays a crucial role in the creation of innovative materials and technologies. This compound is an essential resource for scientists working on cutting-edge research projects in Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSemiconductor material development, as it provides a stable base for creating advanced electronic components.\u003c\/li\u003e\n\u003cli\u003eOptical component synthesis, due to its ability to be modified for unique optical properties.\u003c\/li\u003e\n\u003cli\u003eChemical modification studies, as it can form bonds with various functional groups for tailored applications.\u003c\/li\u003e\n\u003cli\u003eResearch in advanced materials, where its molecular structure supports the creation of new material properties.\u003c\/li\u003e\n\u003cli\u003eMolecular synthesis experiments, as it serves as a flexible building block for complex compound creation.\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: 4569-45-3\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Material Building Blocks \u0026gt; Small Molecule Semiconductor Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e9,9-Dimethylfluorene 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 potential reactivity, it should be handled in a well-ventilated area, preferably with appropriate personal protective equipment. Avoid contact with incompatible substances to ensure safety during storage and use. Regular inspection of storage conditions is advised to maintain the integrity of the compound. Proper labeling and secure storage are essential to prevent accidental exposure and ensure safe laboratory practices.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086604710106,"sku":"TCI2510D323523485","price":816000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086604742874,"sku":"TCI2510D323523486","price":2390000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3235.jpg?v=1768817844"},{"product_id":"tci2510d355723866","title":"TCI D3557 14348-75-5 2,7-Dibromo-9-fluorenone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D3557 2,7-Dibromo-9-fluorenone is a polycyclic aromatic intermediate that serves as a backbone material in a great deal of organic electronics research. The molecule consists of a fluorenone core carrying two bromine atoms at the 2 and 7 positions together with a single ketone group at position 9. This symmetrical arrangement provides two equivalent attachment points for cross-coupling reactions, along with one reactive carbonyl centre in the middle of the structure. For this reason, the compound is frequently used as the starting core in the construction of conjugated polymers, light-emitting oligomers, and organic ligands built on rigid frameworks.\u003c\/p\u003e\n\u003cp\u003eThe properties that make this compound a preferred choice are the planar rigidity of the fluorenone core and the electron-withdrawing capability of its carbonyl group. This combination produces an effective electron-acceptor unit in the design of donor–acceptor systems, so that the energy gap and absorption characteristics of the final material can be tuned. Its two aryl bromine atoms are highly responsive to Suzuki, Stille, and Sonogashira reactions as well as Yamamoto polymerisation, allowing conjugation to be extended in a controlled manner. The ketone group at position 9 can also be attacked by organolithium or Grignard nucleophiles to form 9,9-disubstituted derivatives that improve solubility and prevent chain aggregation.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically found in university and institutional research groups working on organic semiconductors, materials chemistry, and synthetic methodology. It is commonly handled at bench scale for the preparation of monomers and small libraries of derivatives, usually under inert-atmosphere technique in a fume hood. Researchers preparing publications, theses, or collaborative materials-science projects rely on a defined-quality reagent of this type so that coupling results remain reproducible between batches and between laboratories.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSuzuki cross-coupling monomer synthesis: the two equivalent aryl bromide sites react cleanly with boronic acids, giving symmetrical extended aromatic products that are ideal for building conjugated backbones.\u003c\/li\u003e\n\u003cli\u003eYamamoto and Stille polymerisation: the symmetrical dibromide functions as a difunctional monomer, allowing controlled chain growth into conjugated polymers with a repeating fluorenone acceptor unit along the main chain.\u003c\/li\u003e\n\u003cli\u003eDonor–acceptor system design: the electron-withdrawing carbonyl group at position 9 acts as an acceptor moiety, letting researchers tune the energy gap and absorption profile of the target material.\u003c\/li\u003e\n\u003cli\u003eSonogashira alkynylation chemistry: both bromine positions couple with terminal alkynes to introduce rigid acetylenic linkers, extending conjugation length in light-emitting oligomers and related structures.\u003c\/li\u003e\n\u003cli\u003e9,9-Disubstituted derivative preparation: the reactive ketone centre is readily attacked by organolithium or Grignard reagents, producing substituted derivatives with improved solubility and reduced chain aggregation.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eCAS Number: 14348-75-5\u003c\/li\u003e\n\u003cli\u003eChemical name: 2,7-Dibromo-9-fluorenone\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research-scale packaging; please confirm the currently offered pack size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep the container tightly closed in a cool, dry, well-ventilated place away from light\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 and well-ventilated area, protected from direct sunlight and away from strong oxidising agents, strong bases and sources of ignition. Keep the material in its original amber or opaque supplier container, or transfer it to a clean, dry, chemically compatible glass vessel with a secure closure; label all secondary containers clearly. Handle the solid in a fume hood to avoid generating or inhaling dust, and wear safety glasses, nitrile gloves and a laboratory coat throughout weighing and transfer operations. Because the compound is moisture- and air-sensitive in subsequent coupling steps, allow sealed containers to warm to room temperature before opening to prevent condensation, and reseal promptly after use. Consult the manufacturer's safety data sheet before first use, and dispose of residues and contaminated consumables as halogenated organic chemical waste in line with institutional procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086624403674,"sku":"TCI2510D355723866","price":1350000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086624436442,"sku":"TCI2510D355723867","price":4049000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3557.jpg?v=1767106241"},{"product_id":"tci2510d358623906","title":"TCI D3586 20302-14-1 9,9-Diphenylfluorene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D3586 9,9-Diphenylfluorene, CAS 20302-14-1, is an aromatic hydrocarbon compound built on a fluorene skeleton with two phenyl groups bonded to the carbon atom at the 9-position. The compound is an important building block in materials science, particularly for the development of organic semiconductors such as OLED materials, organic field-effect transistors, and organic solar cells. The fluorene framework provides a rigid conjugated system with strong emission in the blue region, while the diphenyl substitution at the 9-position locks the molecular conformation, prevents interchain aggregation, and suppresses the formation of ketone defects that commonly degrade the colour purity of blue emission.\u003c\/p\u003e\n\u003cp\u003eThe characteristics that make this material a widely preferred choice are its high thermal and morphological stability. The sp3 configuration at carbon 9, which binds two phenyl groups, produces a three-dimensional propeller-like geometry, so that the thin films formed tend to be amorphous and resistant to crystallisation during device operation. This property directly influences device service life. In addition, positions 2 and 7 on the fluorene skeleton remain open for halogenation, boronation, and cross-coupling reactions, making this compound a versatile synthetic starting point for constructing larger conjugated architectures.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is typically used in university and institutional research groups working on organic electronics, photophysics, and synthetic materials chemistry. It serves as a starting material in multi-step syntheses of functionalised fluorene derivatives, as a model compound in studies of blue emission and conformational effects, and as a reference structure in coursework and thesis-level research on conjugated small molecules and organic semiconductor design.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOLED material development: the rigid fluorene core emits strongly in the blue region while the 9,9-diphenyl substitution suppresses ketone defect formation that degrades blue colour purity.\u003c\/li\u003e\n\u003cli\u003eOrganic field-effect transistor research: the conjugated fluorene framework supports charge transport, and the amorphous, crystallisation-resistant film morphology helps maintain consistent device behaviour during operation.\u003c\/li\u003e\n\u003cli\u003eOrganic solar cell studies: the compound functions as a conjugated building block for donor and acceptor architectures where thermal and morphological stability of the active layer matters.\u003c\/li\u003e\n\u003cli\u003eCross-coupling and functionalisation chemistry: the open 2- and 7-positions on the fluorene skeleton accept halogenation, boronation, and cross-coupling reactions for building larger conjugated systems.\u003c\/li\u003e\n\u003cli\u003ePhotophysical and conformational model studies: the propeller-like three-dimensional geometry at the sp3 carbon makes this an instructive reference compound for investigating aggregation suppression and conformational locking.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eCAS number: 20302-14-1\u003c\/li\u003e\n\u003cli\u003eProduct code: D3586\u003c\/li\u003e\n\u003cli\u003eChemical name: 9,9-Diphenylfluorene\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Material Building Blocks \u0026gt; Small Molecule Semiconductor Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research-scale packaging; please confirm the size required when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a cool, dry place in the original tightly closed container\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the container in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and strong oxidising agents. Keep the material in its original tightly closed container, or in a clean amber glass or chemically compatible bottle if transferred, to limit exposure to moisture and light. Handle in a fume hood and use standard personal protective equipment, including safety glasses, nitrile gloves, and a laboratory coat. Avoid generating and inhaling dust when weighing the solid, and clean spills promptly using dry collection methods. Wash hands thoroughly after handling, keep the container clearly labelled, and always consult the manufacturer's safety data sheet before use and before disposal of residues.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086627909850,"sku":"TCI2510D358623906","price":2671000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086627942618,"sku":"TCI2510D358623907","price":8517000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D3586.jpg?v=1769180615"},{"product_id":"tci2510d408424567","title":"TCI D4084 58775-05-6 2,7-Di-tert-butylfluorene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D4084 with CAS number 58775-05-6 is 2,7-Di-tert-butylfluorene, a fluorene derivative carrying two tert-butyl groups at the 2 and 7 positions of the aromatic ring system. The compound belongs to the class of non-heterocyclic building blocks and is widely used as a core scaffold in organic materials chemistry. The fluorene core itself is a bridged biphenyl system that is rigid, fully conjugated, and characterised by distinctive blue fluorescence, which has made it one of the most popular motifs in the development of optoelectronic materials, fluorescence sensors, and conjugated polymers in materials research laboratories.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this compound a preferred choice is the presence of the two tert-butyl groups, which work on two fronts at once. First, these groups improve solubility in common organic solvents, so that derivative products are easier to process through solution-based techniques such as spin coating. Second, the bulky tert-butyl groups provide steric hindrance that helps prevent intermolecular stacking, or aggregation, which is the cause of fluorescence quenching and unwanted spectral shifts. In addition, because the 2 and 7 positions are already substituted, subsequent reactions are directed toward the C-9 position on the methylene bridge, giving chemists predictable regiochemical control over further functionalisation.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2,7-Di-tert-butylfluorene is typically encountered in university and institutional research groups working on organic materials chemistry, particularly those developing optoelectronic materials, fluorescence-based sensors, and conjugated polymers. It is used as a starting scaffold in synthetic work rather than as a routine analytical reagent, so it is generally ordered in research-scale quantities by synthesis laboratories that already have facilities for handling organic building blocks and for solution processing of the resulting derivatives.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eConjugated polymer synthesis — the rigid, fully conjugated fluorene core serves as a repeating unit, while the tert-butyl groups keep the resulting polymer soluble enough for solution processing.\u003c\/li\u003e\n\u003cli\u003eOptoelectronic materials development — the characteristic blue fluorescence of the fluorene system makes this building block a common starting point for emissive layer materials in research-scale device work.\u003c\/li\u003e\n\u003cli\u003eFluorescence sensor construction — the intrinsic blue emission of the fluorene core provides the optical signal, and the tert-butyl substitution helps preserve emission intensity by limiting aggregation-driven quenching.\u003c\/li\u003e\n\u003cli\u003eC-9 selective functionalisation studies — with the 2 and 7 positions already occupied, subsequent chemistry is directed to the methylene bridge, giving predictable regiochemistry for building more complex scaffolds.\u003c\/li\u003e\n\u003cli\u003eSolution-processed thin film preparation — improved solubility in common organic solvents allows derivatives to be deposited by techniques such as spin coating without additional solubilising modifications.\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: 58775-05-6\u003c\/li\u003e\n\u003cli\u003eChemical name: 2,7-Di-tert-butylfluorene\u003c\/li\u003e\n\u003cli\u003eCatalogue reference: D4084\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in research-scale laboratory pack sizes; please confirm the currently available packaging when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the manufacturer's instructions on the product label and safety data sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the product in its original tightly closed container in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and incompatible materials, following the storage conditions stated by the manufacturer on the label and in the safety data sheet. Keep the container sealed when not in use to prevent moisture uptake and contamination of the material. Handle the compound in a fume hood using appropriate personal protective equipment, including safety glasses, gloves, and a laboratory coat, and avoid the generation and inhalation of dust during weighing and transfer. Use clean, dry spatulas and glassware suitable for organic solids, label all secondary containers clearly, and dispose of residues and contaminated materials in accordance with applicable laboratory chemical waste procedures. Always review the full safety data sheet before first use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086654812378,"sku":"TCI2510D408424567","price":1322000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086654845146,"sku":"TCI2510D408424568","price":4414000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4084.jpg?v=1767107041"},{"product_id":"tci2510d432724891","title":"TCI D4327 123863-97-8 9,9-Dihexylfluorene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D4327 9,9-Dihexylfluorene (CAS 123863-97-8) is a fluorene derivative carrying two hexyl chains at the 9-position. The compound belongs to the family of small molecule semiconductor building blocks and serves as an important base material in organic electronics research. The fluorene framework provides a biphenyl conjugated system that is locked into a coplanar geometry by a methylene bridge, giving rise to efficient blue emission and good charge carrier mobility. In the laboratory, this compound is used as a starting material that is subsequently halogenated, borylated, or polymerised into functional materials.\u003c\/p\u003e\n\u003cp\u003eThe characteristic that makes it a preferred choice is the role of the two hexyl chains on the C9 carbon. These alkyl chains project perpendicular to the plane of conjugation, so they do not disturb the electronic properties of the fluorene core, yet they dramatically improve solubility in organic solvents such as toluene, chloroform, and tetrahydrofuran. This good solubility is precisely what enables solution-based processing methods such as spin coating and inkjet printing during device fabrication. In addition, the double substitution at C9 prevents the formation of fluorenone groups through oxidation, a defect known to produce an undesirable green emission band.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 9,9-dihexylfluorene is typically handled in university and institutional research groups working on organic electronics, polymer chemistry, and photonic materials. It is generally used at small synthetic scale inside a fume hood, as the entry point of a multi-step route toward monomers and conjugated polymers. Groups preparing thin films for optoelectronic testing rely on it where reproducible, solution-processable fluorene chemistry is required.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eConjugated polymer synthesis: it acts as the parent fluorene unit that is functionalised into monomers and then polymerised, giving research groups a reliable entry point into polyfluorene chemistry.\u003c\/li\u003e\n\u003cli\u003eBlue-emitting material development: the coplanar fluorene framework provides efficient blue emission, so the compound underpins studies on emissive layers for organic light-emitting device research.\u003c\/li\u003e\n\u003cli\u003eHalogenation and borylation chemistry: the molecule is routinely brominated or converted to boronate esters, supplying the coupling partners needed for building larger conjugated architectures.\u003c\/li\u003e\n\u003cli\u003eSolution-processed thin film fabrication: the hexyl chains give solubility in toluene, chloroform, and tetrahydrofuran, allowing spin coating and inkjet printing of uniform semiconductor films.\u003c\/li\u003e\n\u003cli\u003eCharge transport and photophysics studies: good carrier mobility combined with resistance to fluorenone defect formation makes it suitable for investigating structure–property relationships in organic semiconductors.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eCAS number: 123863-97-8\u003c\/li\u003e\n\u003cli\u003eChemical name: 9,9-Dihexylfluorene\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Material Building Blocks \u0026gt; Small Molecule Semiconductor Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research-scale catalogue pack sizes; please confirm the required size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a tightly closed original container, protected from light and air\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the material in its original tightly closed container in a cool, dry, well-ventilated area away from light, heat, and sources of ignition. Amber glass or the supplier's sealed container is suitable, and headspace should be minimised for material intended for device work, since oxidative contamination can compromise optoelectronic performance. Handle and weigh the compound inside a fume hood, wearing safety glasses, a laboratory coat, and chemically resistant gloves. Avoid inhalation of dust and contact with skin and eyes, keep it separated from strong oxidising agents, and dispose of residues and contaminated consumables through the laboratory's chemical waste stream. Always consult the manufacturer's safety data sheet before first use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086687088858,"sku":"TCI2510D432724891","price":1827000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086687121626,"sku":"TCI2510D432724892","price":6213000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4327.jpg?v=1769141981"},{"product_id":"tci2510d457325203","title":"TCI D4573 853234-57-8 2,8-Dibromoindeno[1,2-b]fluorene-6,12-dione","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2,8-Dibromoindeno[1,2-b]fluorene-6,12-dione is a complex chemical compound widely used in scientific research related to semiconductor materials and material synthesis. This compound plays a crucial role in laboratories where the development of advanced materials with specific electronic properties is required. Its unique molecular structure makes it an essential building block for creating new materials with tailored functionalities. Due to its stability and reactivity, it is frequently used in the synthesis of complex compounds, particularly in the fields of materials science and nanotechnology.\u003c\/p\u003e\n\u003cp\u003eThe compound's chemical properties, including its stability and ability to interact with various reagents, make it a preferred choice for high-precision experiments. Its molecular structure allows for chemical modifications through specific reactions, which is highly beneficial in the development of new materials. This versatility enables researchers to explore new applications in electronic components and advanced material systems. The compound's reliability and consistency in experimental settings ensure accurate and reproducible results.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2,8-Dibromoindeno[1,2-b]fluorene-6,12-dione is commonly used in applied material technology research, especially in the development of semiconductor materials and electronic components. It is also frequently found in projects related to energy and environmental innovation, where its chemical properties contribute to the creation of sustainable and efficient materials.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSemiconductor material synthesis due to its unique molecular structure and chemical reactivity.\u003c\/li\u003e\n\u003cli\u003eDevelopment of advanced electronic components through precise chemical modifications.\u003c\/li\u003e\n\u003cli\u003eResearch in nanotechnology for creating novel materials with specific electronic properties.\u003c\/li\u003e\n\u003cli\u003eEnvironmental and energy innovation projects requiring stable and reactive chemical compounds.\u003c\/li\u003e\n\u003cli\u003eApplied material science experiments focusing on the synthesis of complex molecular structures.\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: 853234-57-8\u003c\/li\u003e\n\u003cli\u003eCategory: Materials Science \u0026gt; Material Building Blocks \u0026gt; Small Molecule Semiconductor Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, as per standard chemical compound properties\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry, and well-ventilated area away from light and heat\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry, and well-ventilated area, away from direct light and heat sources. It is recommended to use airtight containers made of materials compatible with its chemical properties to prevent degradation. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Storage conditions should maintain a stable environment to preserve its integrity and effectiveness. Regular inspection of storage containers is advised to ensure no contamination or exposure occurs. Proper labeling of containers is essential for safe handling and easy identification.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086697836762,"sku":"TCI2510D457325203","price":5735000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D4573.jpg?v=1769142011"},{"product_id":"tci2510d500925807","title":"TCI D5009 462128-39-8 2-(9,9-Diphenyl-9H-fluoren-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-(9,9-Diphenyl-9H-fluoren-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron compound widely used in chemical research, particularly in organic synthesis. This reagent plays a crucial role in various reactions, including S-N coupling and Suzuki reactions, which are essential for constructing complex molecular structures. Its unique chemical structure, combining a fluorene group with a dioxaborolane moiety, provides both reactivity and stability, making it a versatile tool in synthetic chemistry.\u003c\/p\u003e\n\u003cp\u003eThe compound is favored for its ability to participate in multiple functional group reactions, offering high efficiency and selectivity in laboratory settings. Its molecular design allows for compatibility with a wide range of substrates, enabling chemists to achieve desired products with minimal side reactions. The compound’s stability under certain reaction conditions further enhances its reliability, making it a preferred choice for researchers aiming to optimize synthetic pathways.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in the synthesis of complex compounds and drug development. Its role in facilitating efficient and selective chemical transformations has made it a valuable asset in academic and industrial research environments. The compound is also utilized in studies involving reactions that require controlled reactivity and stability, contributing to the advancement of chemical sciences in the region.\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 participate in coupling reactions, enabling the formation of complex molecular structures with high efficiency.\u003c\/li\u003e\n\u003cli\u003eDrug development research utilizes this reagent for constructing diverse molecular frameworks, supporting the creation of novel pharmaceutical compounds.\u003c\/li\u003e\n\u003cli\u003eS-N coupling reactions rely on its reactivity and stability, making it an essential component in the synthesis of nitrogen-containing organic molecules.\u003c\/li\u003e\n\u003cli\u003eSuzuki cross-coupling reactions leverage its compatibility with various substrates, allowing for the efficient formation of carbon-carbon bonds.\u003c\/li\u003e\n\u003cli\u003eResearch on functional group transformations benefits from its versatility, enabling chemists to explore a wide range of synthetic strategies.\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: 462128-39-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from moisture and direct sunlight to maintain its chemical integrity. It is recommended to use airtight containers made of materials that are chemically inert, such as glass or polyethylene, to prevent any unwanted reactions. Due to its organoboron nature, it is important to handle it with care, using appropriate personal protective equipment like gloves and goggles. The compound should not be exposed to strong oxidizing agents or incompatible substances. Regular monitoring of storage conditions is advised to ensure optimal stability and safety in the laboratory setting.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086739747034,"sku":"TCI2510D500925807","price":704000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086739779802,"sku":"TCI2510D500925808","price":2559000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5009.jpg?v=1769142067"},{"product_id":"tci2510d501825820","title":"TCI D5018 569343-09-5 2-(9,9-Dimethyl-9H-fluoren-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D5018, with the CAS number 569343-09-5, is a highly specialized organoboron reagent used in advanced chemical reactions within laboratory settings. This compound, known as 2-(9,9-Dimethyl-9H-fluoren-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, plays a crucial role in synthetic chemistry, particularly in the field of organoboron reagents. It is widely utilized in the synthesis of complex organic molecules, including aromatic and heterocyclic compounds, due to its unique chemical structure and reactivity. Its application is especially prominent in the Suzuki reaction, a key method in modern organic synthesis.\u003c\/p\u003e\n\u003cp\u003eThe compound's molecular structure combines a fluorene group with a boronic acid derivative, offering both stability and reactivity. This dual functionality makes it a preferred choice for chemists seeking efficient and specific chemical transformations. The compound's ability to participate in cross-coupling reactions, particularly with aryl halides, allows for the formation of carbon-carbon bonds under mild conditions. Its high reactivity and compatibility with various reaction conditions contribute to its popularity in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, TCI D5018 is a staple in organic chemistry research, particularly in the development of pharmaceutical compounds and advanced materials. Its stability and versatility make it a reliable reagent for complex synthetic pathways. Researchers in Indonesia frequently use it in academic and industrial settings to achieve precise and efficient chemical syntheses. Its widespread application underscores its importance in the field of chemical innovation and research.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSuzuki Reaction: This reagent is ideal for cross-coupling reactions that require high reactivity and specificity, making it essential for the synthesis of aromatic and heterocyclic compounds.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis: Its unique molecular structure enables efficient formation of carbon-carbon bonds, supporting the creation of complex organic molecules in laboratory settings.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: The compound is frequently used in the development of new drug compounds due to its ability to participate in precise and controlled chemical transformations.\u003c\/li\u003e\n\u003cli\u003eMaterial Science: Its reactivity and stability make it suitable for the synthesis of advanced materials, including polymers and functional compounds.\u003c\/li\u003e\n\u003cli\u003eAcademic Research: It is a preferred choice in Indonesian universities and research institutions for its reliability and effectiveness in complex chemical reactions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS Number: 569343-09-5\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron\u003c\/li\u003e\n\u003cli\u003ePack Sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical Form: Solid or liquid, depending on the specific formulation\u003c\/li\u003e\n\u003cli\u003eStorage Note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis reagent 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 could affect its chemical integrity. Due to its organoboron nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to keep the compound away from incompatible substances and ensure proper ventilation in the laboratory. Regular inspection of storage conditions is advised to ensure the reagent remains in optimal condition for use in chemical reactions.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086740271322,"sku":"TCI2510D501825820","price":1659000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086740304090,"sku":"TCI2510D501825821","price":5819000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5018.jpg?v=1771058789"},{"product_id":"tci2510d503325845","title":"TCI D5033 1259280-37-9 2-(9,9-Diphenyl-9H-fluoren-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eThis chemical compound, 2-(9,9-Diphenyl-9H-fluoren-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, is a key organoboron reagent widely used in laboratory settings. It plays a critical role in synthetic chemistry, particularly in the development of complex organic molecules. As a boronic acid derivative, it is essential in catalytic reactions that require metal-based catalysts. Its unique molecular structure allows it to participate in various organic transformations, making it a versatile tool for chemists.\u003c\/p\u003e\n\u003cp\u003eThe compound is favored for its stability under controlled conditions and its ability to undergo efficient reactions in the presence of transition metal catalysts. Its molecular design enables it to act as a coupling partner in cross-coupling reactions, such as the Suzuki-Miyaura reaction. This reactivity makes it an ideal choice for researchers aiming to synthesize a wide range of organic compounds. Its reliability and consistent performance in laboratory experiments further enhance its appeal among chemists.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is commonly used in academic and industrial research settings. It supports the development of pharmaceutical compounds, functional materials, and advanced chemical syntheses. Its presence in research institutions and chemical laboratories underscores its importance in advancing chemical innovation and scientific discovery in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from this reagent’s ability to form carbon-carbon bonds efficiently, enabling the creation of complex molecular structures.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes this compound in the development of drug molecules, where precise chemical modifications are essential.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical processes incorporate this reagent for the production of specialty chemicals and materials with specific functional properties.\u003c\/li\u003e\n\u003cli\u003eAcademic research institutions use it to explore new synthetic methodologies and catalytic mechanisms in organic chemistry.\u003c\/li\u003e\n\u003cli\u003eMaterial science laboratories employ it in the synthesis of advanced polymers and nanomaterials requiring controlled chemical reactivity.\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: 1259280-37-9\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 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 environment to maintain its chemical stability. It is recommended to keep it in airtight containers to prevent exposure to moisture and air, which may affect its reactivity. Proper labeling of storage containers is essential for safety and identification. In laboratory settings, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to minimize direct contact. Storage conditions should avoid extreme temperatures and direct sunlight to preserve its integrity. Regular inspection of storage areas ensures compliance with safety standards and prevents potential chemical degradation.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086741090522,"sku":"TCI2510D503325845","price":1857000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086741123290,"sku":"TCI2510D503325846","price":6437000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5033.jpg?v=1768205087"},{"product_id":"tci2510d512525964","title":"TCI D5125 112486-09-6 7,7-Dimethyl-7H-benzo[c]fluorene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e7,7-Dimethyl-7H-benzo[c]fluorene is a chemical compound widely used as a building block in the synthesis of complex molecules. This compound plays a vital role in organic chemistry laboratories, where it serves as a key component in the development of structurally intricate compounds. Its aromatic structure and specific substituents make it an essential tool for researchers aiming to create compounds with tailored properties. Due to its stability and reactivity, it is frequently employed in various synthetic pathways that require controlled chemical transformations.\u003c\/p\u003e\n\u003cp\u003eThe compound's unique chemical properties, including its aromatic stability and reactivity, make it a preferred choice for organic synthesis. The presence of methyl groups at the 7-position enhances its reactivity compared to similar compounds, allowing it to participate in a range of reactions such as substitution, oxidation, and reduction. These characteristics make it particularly valuable in research settings where precise chemical modifications are required. Its versatility and predictable behavior under different reaction conditions contribute to its widespread use in both academic and industrial laboratories.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 7,7-Dimethyl-7H-benzo[c]fluorene is commonly used in organic chemistry research, especially in pharmaceutical and materials science applications. It is a staple in academic institutions and research centers across Indonesia, where it supports the development of new compounds with potential applications in medicine and industry. Its role in synthesizing complex molecules makes it an indispensable resource for scientists working on innovative chemical projects.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of complex molecules where aromatic structures with specific substitutions are required.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceutical compounds that rely on precise molecular frameworks and functional groups.\u003c\/li\u003e\n\u003cli\u003eResearch in materials science for the creation of advanced polymers and functional materials.\u003c\/li\u003e\n\u003cli\u003eInvestigation of chemical reactivity patterns in aromatic compounds with methyl substitutions.\u003c\/li\u003e\n\u003cli\u003eExploration of catalytic processes involving stable aromatic intermediates in synthetic pathways.\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: 112486-09-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct sunlight and moisture. It is recommended to use airtight containers to prevent exposure to air and humidity, which could affect its stability. Due to its chemical nature, it should be handled with appropriate personal protective equipment, including gloves and safety goggles. It is important to ensure that the storage area is well-ventilated to minimize any potential risks associated with its handling. The compound should not be stored near incompatible substances, such as strong oxidizers or acids, to avoid any chemical interactions. Proper labeling of containers is essential for safe handling and to prevent accidental exposure.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086745612506,"sku":"TCI2510D512525964","price":2306000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086745645274,"sku":"TCI2510D512525965","price":8124000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5125.jpg?v=1767108423"},{"product_id":"tci2510d530126175","title":"TCI D5301 216312-73-1 3,6-Dibromo-9H-fluoren-9-one","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3,6-Dibromo-9H-fluoren-9-one is a chemical compound widely used in organic synthesis reactions within laboratory settings. This compound belongs to the category of non-heterocyclic building blocks and is valued for its structural versatility and reactivity. Its aromatic structure, with bromo substituents at positions 3 and 6, makes it a key reagent in various synthetic pathways. In research and development, it serves as a foundational material for the creation of more complex chemical structures. Its role is critical in the synthesis of heterocyclic compounds and other intricate molecular frameworks.\u003c\/p\u003e\n\u003cp\u003eThe compound’s stability and reactivity make it a preferred choice for laboratory applications. The aromatic nature of 3,6-Dibromo-9H-fluoren-9-one allows it to participate in substitution and electrophilic reactions, offering researchers control over chemical transformations. Its bromo substituents are particularly useful as they can be readily replaced with a variety of functional groups, enhancing its utility in synthetic chemistry. This adaptability ensures that it remains a valuable tool for chemists working on diverse projects.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 3,6-Dibromo-9H-fluoren-9-one is commonly used in organic chemistry research, especially in the development of complex compounds, pharmaceuticals, and new materials. It is a key component in the synthesis of advanced chemical structures, supporting innovation in both academic and industrial research environments. Its reliability and effectiveness make it a staple in chemical laboratories across Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of complex compounds due to its aromatic structure and bromo substituents.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceuticals as a building block for heterocyclic compound synthesis.\u003c\/li\u003e\n\u003cli\u003eResearch in material science for the creation of advanced chemical structures and polymers.\u003c\/li\u003e\n\u003cli\u003eUse in electrophilic and substitution reactions due to its reactivity and functional group versatility.\u003c\/li\u003e\n\u003cli\u003eSupport for academic and industrial research in chemical innovation and compound development.\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: 216312-73-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in standard laboratory quantities\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e3,6-Dibromo-9H-fluoren-9-one should be stored in a cool, dry environment, away from direct light and moisture. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its bromo substituents, it may react with certain substances, so it should be handled with care in a well-ventilated area. Proper personal protective equipment, such as gloves and safety goggles, should be worn when handling the compound. It is important to ensure that the storage area is secure and not accessible to unauthorized personnel. Regular monitoring of storage conditions will help maintain the compound’s integrity and safety.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086753411290,"sku":"TCI2510D530126175","price":3486000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5301.jpg?v=1767108581"},{"product_id":"tci2510d537126260","title":"TCI D5371 302554-81-0 2-(9,9-Di-n-octyl-9H-fluoren-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eThis chemical compound, known as 2-(9,9-Di-n-octyl-9H-fluoren-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, is a key organoboron reagent widely used in chemical synthesis, particularly in coupling reactions such as the Suzuki-Miyaura reaction. It serves as a versatile tool in organic laboratories, enabling the formation of complex molecules through its reactive boron group. Its structural complexity and stability under controlled conditions make it an essential component in modern synthetic chemistry.\u003c\/p\u003e\n\u003cp\u003eAs an organoboron reagent, this compound is prized for its ability to form stable and reactive intermediates. Its non-mercurial and non-toxic nature enhances its safety profile compared to other organometallic reagents. This makes it a preferred choice for researchers seeking reliable and safe alternatives in their synthetic processes. The compound’s reactivity and stability under specific conditions further contribute to its effectiveness in various chemical applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is commonly used in organic chemistry research, especially in academic and research institutions. Its role in facilitating the synthesis of complex organic compounds aligns with the goals of both educational and industrial research. The compound’s utility in creating new compounds with potential applications in multiple fields underscores its importance in the chemical research landscape of Indonesia.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis applications benefit from this reagent’s ability to participate in coupling reactions, enhancing the efficiency of complex molecule formation.\u003c\/li\u003e\n\u003cli\u003eIt is ideal for Suzuki-Miyaura coupling reactions due to its stability and reactivity, making it a preferred choice in cross-coupling processes.\u003c\/li\u003e\n\u003cli\u003eIn academic research settings, it supports the development of new compounds with potential applications in pharmaceuticals and materials science.\u003c\/li\u003e\n\u003cli\u003eIts non-toxic nature makes it suitable for use in educational laboratories where safety is a priority.\u003c\/li\u003e\n\u003cli\u003eIt is commonly used in the synthesis of functionalized aromatic compounds, offering versatility in reaction pathways.\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: 302554-81-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified in the provided data\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis reagent should be stored in a cool, dry environment, away from moisture and direct sunlight to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and moisture, which could affect its stability. Due to its non-toxic nature, standard laboratory safety protocols should be followed, including proper ventilation and personal protective equipment. While it does not require special handling compared to other organometallic reagents, it is important to ensure that it is kept in a secure location to prevent accidental exposure. Proper storage ensures that the compound remains effective for its intended applications in chemical synthesis.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086756589786,"sku":"TCI2510D537126260","price":3740000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5371.jpg?v=1769142103"},{"product_id":"tci2510d540826301","title":"TCI D5408 1365692-79-0 2-(9,9-Dimethyl-9H-fluoren-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-(9,9-Dimethyl-9H-fluoren-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron compound widely used in organic chemistry laboratories. As a key reagent in organometallic chemistry, it plays a crucial role in various synthetic processes, particularly in cross-coupling reactions. This compound is valued for its ability to participate in complex molecular transformations, making it an essential tool for researchers working on advanced organic synthesis. Its unique structure enables it to interact effectively with transition metals, enhancing the efficiency of chemical reactions.\u003c\/p\u003e\n\u003cp\u003eThe compound's stability and controlled reactivity make it a preferred choice for precision-based applications. It is known for its ability to remain intact under various reaction conditions while still being reactive enough to facilitate desired chemical transformations. This balance between stability and reactivity is critical in modern synthetic chemistry, where accuracy and reproducibility are paramount. Additionally, its compatibility with palladium-based catalysts makes it ideal for use in reactions such as Suzuki-Miyaura and Kumada-Corriu coupling.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in the synthesis of heterocyclic compounds and bioactive molecules. Its availability in the local market supports scientific research and development efforts, enabling researchers to conduct high-precision experiments. Its application in pharmaceutical and biochemical studies further highlights its importance in both academic and industrial settings.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSuzuki-Miyaura coupling reactions for the synthesis of heterocyclic compounds due to its compatibility with palladium catalysts and high reactivity.\u003c\/li\u003e\n\u003cli\u003eKumada-Corriu coupling applications in the development of bioactive molecules, leveraging its ability to form stable carbon-metal bonds.\u003c\/li\u003e\n\u003cli\u003eOrganic synthesis of complex molecules requiring precise chemical transformations, benefiting from its controlled reactivity and stability.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research for the creation of drug candidates, as it supports the formation of diverse molecular structures.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies involving the synthesis of active compounds, where its reactivity and structural versatility are highly advantageous.\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: 1365692-79-0\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on formulation\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its stability and reactivity. It is recommended to keep it in a tightly sealed container to prevent exposure to moisture and air, which can affect its chemical integrity. Due to its potential reactivity with certain materials, it is best stored in a chemically inert container such as glass or polyethylene. Laboratory personnel should handle the compound with care, using appropriate personal protective equipment to ensure safety. Regular monitoring of storage conditions is advised to maintain optimal performance in experimental applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48086757933274,"sku":"TCI2510D540826301","price":2531000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086757966042,"sku":"TCI2510D540826302","price":8826000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5408.jpg?v=1771058463"},{"product_id":"tci2510d544826341","title":"TCI D5448 132717-37-4 2,7-Dibromo-9-phenyl-9H-fluoren-9-ol","description":"\u003cp\u003e\u003cstrong\u003e2,7-Dibromo-9-phenyl-9H-fluoren-9-ol\u003c\/strong\u003e (CAS 132717-37-4) is a high-quality chemical from TCI, supplied as \u003cstrong\u003eGC Grade \/ for Synthesis\u003c\/strong\u003e.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eApplication:\u003c\/strong\u003e Aromatic carbocyclic compound serving as a core scaffold in organic and materials synthesis.\u003c\/p\u003e\u003cp\u003e\u003cstrong\u003eSpecifications:\u003c\/strong\u003e\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003eMolecular formula: C19H12Br2O\u003c\/li\u003e\n\u003cli\u003eCAS number: 132717-37-4\u003c\/li\u003e\n\u003cli\u003ePurity: \u0026gt;98.0%(GC)\u003c\/li\u003e\n\u003cli\u003eTCI product code: D5448\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003e\u003cstrong\u003eSynonyms:\u003c\/strong\u003e 2,7-Dibromo-9-hydroxy-9-phenyl-9H-fluorene\u003c\/p\u003e\u003cp\u003eAvailable from \u003cstrong\u003eAMI Scientific\u003c\/strong\u003e, the authorised TCI distributor in Indonesia. \u003cstrong\u003eContact us for pricing and stock availability\u003c\/strong\u003e — we ship throughout Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086759637210,"sku":"TCI2510D544826341","price":1857000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086759669978,"sku":"TCI2510D544826342","price":6297000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5448.jpg?v=1768818425"},{"product_id":"tci2510d567126645","title":"TCI D5671 198142-65-3 2,7-Dibromospiro[9H-fluorene-9,9'-[9H]xanthene]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D5671, 2,7-Dibromospiro[9H-fluorene-9,9'-[9H]xanthene], is a spiro-configured aromatic compound that joins a fluorene framework and a xanthene framework through a single shared carbon atom, with two bromine atoms attached at the two and seven positions of the fluorene ring. The material is classified as a heterocyclic building block and serves in the laboratory as a central core for assembling large, three-dimensionally shaped molecules, particularly in organic materials research directed toward electronics. The two available bromine atoms act as ready-to-use connection points in catalytic coupling reactions used to attach charge-carrying units or light-emitting units to the core.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this compound distinctive is its spiro geometry, which forces the two aromatic planes to stand almost perpendicular to one another. That arrangement prevents molecules from stacking tightly against each other in the solid state, so the thin films formed from such materials tend to be amorphous, thermally stable, and resistant to the crystalline aggregation that degrades device performance. In addition, the oxygen atom in the xanthene ring donates electrons, allowing the electronic character of the core to be tuned. The uniform dibromo reactivity at the symmetric two and seven positions supports predictable, controlled substitution on both arms of the fluorene unit.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this building block is typically used by university and institutional research groups working on organic electronic materials, where a rigid, non-planar aromatic core is needed as the starting point for a synthetic route. It is generally ordered in research-scale quantities for method development, small-batch synthesis, and the preparation of intermediates that are later characterized and used in thin-film studies. Its role is that of a specialist synthetic input rather than a routine bulk reagent.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSuzuki–Miyaura and related cross-coupling synthesis: the two aryl bromide positions provide clean, equivalent handles for attaching boronic acid or ester partners under palladium catalysis.\u003c\/li\u003e\n\u003cli\u003eHost and charge-transport material development: the perpendicular spiro core suppresses close molecular packing, helping researchers build amorphous films with good thermal behaviour for device layers.\u003c\/li\u003e\n\u003cli\u003eEmitter scaffold construction: the symmetric dibromo substitution allows two identical light-emitting or auxiliary units to be installed on a single rigid three-dimensional core.\u003c\/li\u003e\n\u003cli\u003eStructure–property relationship studies: the electron-donating xanthene oxygen lets research groups systematically tune the electronic character of the core and compare resulting derivatives.\u003c\/li\u003e\n\u003cli\u003ePreparation of higher intermediates and monomers: the compound acts as a central starting block for multi-step routes toward larger spiro-based aromatic architectures.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eCAS number: 198142-65-3\u003c\/li\u003e\n\u003cli\u003eCatalogue reference: D5671\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: research-scale packs as listed by the manufacturer for this catalogue item\u003c\/li\u003e\n\u003cli\u003eStorage: keep in the closed original container under the conditions stated on the manufacturer label and safety data sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the compound in its original tightly closed container in a cool, dry, well-ventilated chemical store, away from light, moisture, heat sources, and incompatible materials, following the conditions printed on the manufacturer label and safety data sheet. Amber glass or the supplied container is suitable; transfer with clean, dry glass or stainless spatulas to avoid contamination. Handle the solid inside a fume hood, wearing a laboratory coat, nitrile gloves, and safety glasses, and avoid generating or inhaling dust. Read the safety data sheet before first use, keep containers clearly labelled, and collect residues and contaminated consumables as halogenated organic chemical waste for disposal through the institution's approved route.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086774612186,"sku":"TCI2510D567126645","price":2222000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086774644954,"sku":"TCI2510D567126646","price":8629000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5671.jpg?v=1767109064"},{"product_id":"tci2510d580026785","title":"TCI D5800 1005771-03-8 2-[3-(9,9-Dimethyl-9H-fluoren-2-yl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D5800, 2-[3-(9,9-Dimethyl-9H-fluoren-2-yl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (CAS 1005771-03-8), is an organoboron reagent in the form of a pinacol boronate ester carrying a biphenyl-fluorene unit. In the synthesis laboratory, this compound serves as the nucleophilic partner in cross-coupling reactions, supplying the aromatic fragment that is joined to an aryl halide or triflate. The 9,9-dimethylfluorene unit it carries is a structural motif well known in materials chemistry, because its framework is rigid and conjugated, while the dimethyl groups at position 9 help maintain solubility and prevent molecular aggregation.\u003c\/p\u003e\n\u003cp\u003eThe property that makes this reagent the preferred choice is its ester form. Compared with free boronic acids, which are often hygroscopic and prone to protodeboronation or to forming boroxines, pinacol esters are generally solids that are far more stable in storage, easy to weigh out accurately, and more tolerant of routine handling at the bench. The ester nevertheless remains reactive under standard Suzuki–Miyaura conditions with a palladium catalyst and a base. The long, partly planar fluorene-phenyl framework contributes the desired optoelectronic character, such as a wide band gap and rigidity along the conjugated backbone.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, a reagent of this type is typically used in university and institutional research groups working on organic synthesis and organic electronic materials, where aryl building blocks are assembled step by step into larger conjugated structures. Its stable ester form suits laboratories that receive shipments over long distances and store reagents for extended periods before use, and it fits naturally into small-scale Suzuki–Miyaura work carried out on a Schlenk line or in a standard inert-atmosphere setup.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSuzuki–Miyaura cross-coupling: the pinacol boronate is the nucleophilic partner that transfers its aryl fragment to an aryl halide or triflate under palladium catalysis with a base, which is precisely the transformation this reagent is designed for.\u003c\/li\u003e\n\u003cli\u003eSynthesis of conjugated organic electronic materials: the rigid, conjugated 9,9-dimethylfluorene framework is a recognised motif in materials chemistry, making this building block suitable for constructing backbones with a wide band gap.\u003c\/li\u003e\n\u003cli\u003eConstruction of extended biaryl architectures: the compound already contains a biphenyl-fluorene unit, so a single coupling step installs a long, partly planar aromatic segment instead of requiring several separate ring-forming operations.\u003c\/li\u003e\n\u003cli\u003ePreparation of soluble, aggregation-resistant conjugated systems: the dimethyl substitution at position 9 of the fluorene helps maintain solubility and prevents molecular aggregation, which matters when target materials must be processed from solution.\u003c\/li\u003e\n\u003cli\u003eReference and comparison work in organoboron methodology: because the pinacol ester resists protodeboronation and boroxine formation better than a free boronic acid, it is a dependable substrate for reproducible coupling studies and condition screening.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (Tokyo Chemical Industry)\u003c\/li\u003e\n\u003cli\u003eCAS number: 1005771-03-8\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003eChemical name: 2-[3-(9,9-Dimethyl-9H-fluoren-2-yl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane\u003c\/li\u003e\n\u003cli\u003ePhysical form: pinacol boronate ester, generally supplied as a solid\u003c\/li\u003e\n\u003cli\u003ePack sizes: research-scale packaging as offered by the manufacturer; please confirm the available pack size when ordering\u003c\/li\u003e\n\u003cli\u003eStorage note: keep in the tightly closed original container, cool, dry, and protected from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the reagent in a cool, dry place inside its tightly closed original container, kept away from moisture, direct sunlight, and sources of heat or ignition. Amber glass or the manufacturer's supplied bottle is appropriate; for long-term storage or after repeated opening, keeping the container under an inert atmosphere and sealed with laboratory film helps limit exposure to atmospheric moisture. Handle the solid in a fume hood or a well-ventilated area, wearing safety glasses, nitrile gloves, and a laboratory coat, and avoid raising dust while weighing. Use clean, dry spatulas and glassware, since traces of water can compromise both the reagent and the coupling reaction. Segregate from strong oxidising agents, collect any spills as dry chemical waste, and consult the manufacturer's Safety Data Sheet before first use and for disposal.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086779330778,"sku":"TCI2510D580026785","price":1659000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086779363546,"sku":"TCI2510D580026786","price":5763000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5800.jpg?v=1769142139"},{"product_id":"tci2510d580126787","title":"TCI D5801 1263001-82-6 9,9-Dimethyl-N-(naphthalen-2-yl)-9H-fluoren-2-amine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI D5801 9,9-Dimethyl-N-(naphthalen-2-yl)-9H-fluoren-2-amine is a secondary aromatic amine that brings together two large aromatic units — a 9,9-dimethylfluorene framework and a 2-naphthyl group — joined through a single nitrogen atom. As a non-heterocyclic building block, this compound serves as a ready-to-use fragment that can be coupled onto larger molecular frameworks, particularly in the preparation of triarylamine materials. The presence of one remaining free N–H bond makes it a direct substrate for metal-catalysed amination reactions, so researchers do not need to construct the diarylamine framework from scratch.\u003c\/p\u003e\n\u003cp\u003eThe properties that make this material a widely preferred choice are its combination of electron richness and structural rigidity. The nitrogen atom of an aromatic amine is electron-donating, so molecules derived from it tend to display low oxidation potentials — a characteristic signature of hole transport materials. The dimethyl-substituted fluorene unit contributes rigidity and thermal stability while preventing molecules from packing too tightly together, whereas the naphthyl unit extends the conjugated system without rendering the molecule difficult to dissolve.\u003c\/p\u003e\n\u003cp\u003eAs a solid that is stable at room temperature, handling is straightforward in a typical Indonesian laboratory setting. It is commonly used in university and institutional research groups working on organic electronic materials, as well as in synthetic chemistry laboratories that assemble arylamine intermediates. Because it arrives as a defined building block, it fits well into laboratories where multi-step synthesis capacity is limited and where a reliable starting fragment shortens the route to the target material.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eTriarylamine synthesis — the free N–H bond allows direct arylation to a third aryl group, giving researchers a shortcut to triarylamine targets without building the diarylamine core first.\u003c\/li\u003e\n\u003cli\u003eHole transport material development — the electron-donating amine nitrogen lowers the oxidation potential of derivatives, which is the key property sought in charge-transporting layers for organic electronic devices.\u003c\/li\u003e\n\u003cli\u003eMetal-catalysed amination studies — as a secondary aromatic amine with a single reactive site, it works as a clean and predictable coupling partner for catalyst screening and reaction optimisation work.\u003c\/li\u003e\n\u003cli\u003eConjugated molecule design — the 2-naphthyl unit extends conjugation across the molecule while keeping solubility workable, so derivatives remain practical to purify and characterise in solution.\u003c\/li\u003e\n\u003cli\u003eThermally robust framework construction — the 9,9-dimethylfluorene core adds rigidity and thermal stability and discourages overly close molecular packing, which suits materials intended for processing and film 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: 1263001-82-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in standard TCI research packaging; please confirm the size required when ordering\u003c\/li\u003e\n\u003cli\u003ePhysical form: solid, stable at room temperature\u003c\/li\u003e\n\u003cli\u003eStorage: keep in a closed original container in a cool, dry place away from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore the material in its original tightly closed container in a cool, dry, and well-ventilated area, protected from direct sunlight and away from strong oxidising agents. Glass or the supplier's original amber packaging is suitable; transfer only what is needed using clean, dry spatulas to avoid moisture pickup and cross-contamination. As with any aromatic amine, weigh and handle the solid inside a fume hood or a well-ventilated bench area, and wear safety glasses, nitrile gloves, and a laboratory coat. Avoid generating and inhaling dust, wash hands after handling, and keep the container clearly labelled. Consult the manufacturer's safety data sheet before use and dispose of residues through your laboratory's chemical waste route.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086779396314,"sku":"TCI2510D580126787","price":1041000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086779429082,"sku":"TCI2510D580126788","price":3542000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510D5801.jpg?v=1768818519"},{"product_id":"tci2510f001729693","title":"TCI F0017 86-73-7 Fluorene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eFluorene, supplied under TCI catalogue code F0017, is a polycyclic aromatic hydrocarbon composed of two benzene rings joined by a single five-membered ring, with a methylene group at the ninth position. This rigid, almost planar structure is what makes it one of the most valuable building blocks in materials chemistry and synthetic organic chemistry. In the laboratory, fluorene serves as a starting material for a wide range of important derivatives, from polyfluorene monomers used in organic electronic device research to the well-known amino-protecting reagents employed in peptide synthesis.\u003c\/p\u003e\n\u003cp\u003eThe property that makes fluorene distinctive is the relative acidity of the proton at the C-9 position. Because the resulting carbanion is stabilised by the two surrounding aromatic rings, this position is readily deprotonated with a strong base and then alkylated to install two substituents at once. That capability allows researchers to tune the solubility and film-forming behaviour of the resulting polymers without disturbing the main conjugated system. In addition, the locked biphenyl framework produces a rigid conjugated system with efficient blue emission, a property highly sought after in the development of organic light-emitting materials.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, fluorene is typically found in university and institutional research groups working on organic synthesis, polymer chemistry, and organic electronic materials, as well as in industrial laboratories that prepare fluorene-based intermediates. It is generally ordered as a research-grade building block for multi-step synthetic routes, for the preparation of derivatives used in peptide chemistry, and for teaching and method-development work in advanced organic chemistry courses.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic electronic materials research, where the rigid biphenyl framework and efficient blue emission make fluorene a preferred precursor for polyfluorene monomers used in light-emitting device studies.\u003c\/li\u003e\n\u003cli\u003ePeptide synthesis support chemistry, since fluorene is the structural parent of the widely used amino-protecting reagents that underpin routine protection and deprotection strategies in peptide work.\u003c\/li\u003e\n\u003cli\u003eC-9 alkylation studies, because the acidic proton at the ninth position is easily deprotonated with a strong base and then alkylated to install two substituents in a single sequence.\u003c\/li\u003e\n\u003cli\u003ePolymer solubility and film-property tuning, as substituents introduced at C-9 adjust solubility and film behaviour without disturbing the main conjugated system of the resulting polymer.\u003c\/li\u003e\n\u003cli\u003eGeneral building-block chemistry in synthetic organic laboratories, where fluorene acts as a starting material for a broad family of derivatives required in multi-step preparative routes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCatalogue code: F0017\u003c\/li\u003e\n\u003cli\u003eCAS number: 86-73-7\u003c\/li\u003e\n\u003cli\u003eChemical name: Fluorene\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: available in the standard TCI catalogue pack sizes; please confirm the packaging option required when ordering\u003c\/li\u003e\n\u003cli\u003eStorage: store according to the conditions stated on the product label and in the accompanying safety data sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore fluorene in its original tightly closed container, in a cool, dry and well-ventilated area away from direct sunlight, heat sources and incompatible materials, following the conditions stated on the product label and safety data sheet. Amber glass or the supplier's original packaging is suitable for keeping the material protected from light and moisture. Handle the solid in a fume hood to limit exposure to dust, and wear standard laboratory personal protective equipment including safety goggles, a laboratory coat and chemical-resistant gloves. Use clean, dry spatulas when weighing to avoid contaminating the bulk stock, close the container immediately after use, and dispose of residues and contaminated materials in accordance with applicable laboratory chemical waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086973972698,"sku":"TCI2510F001729693","price":564000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086974005466,"sku":"TCI2510F001729694","price":3486000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F0017.jpg?v=1767113190"},{"product_id":"tci2510f002129695","title":"TCI F0021 486-25-9 9-Fluorenone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e9-Fluorenone supplied under TCI catalogue code F0021 is a polycyclic aromatic ketone obtained by oxidation at the ninth position of the fluorene skeleton. The carbonyl group is locked inside a five-membered ring and conjugated with two benzene rings, an arrangement that gives the compound its characteristic yellow colour and its notable photochemical behaviour. In the laboratory, 9-fluorenone serves simultaneously as a synthetic building block, a photosensitizer, and an electron acceptor across a wide range of research programmes. This dual role places it on the reagent shelves of organic chemistry laboratories and of materials laboratories working on light-driven energy conversion.\u003c\/p\u003e\n\u003cp\u003eThe property that makes it so widely chosen is the ability of its carbonyl group to absorb visible and ultraviolet light and then enter a relatively long-lived triplet excited state. This excited state can transfer energy to, or draw electrons from, other molecules, which makes the compound an effective initiator of photochemical reactions. Beyond its photochemistry, the carbonyl remains reactive toward nucleophiles, so it is readily converted into alcohols, olefins, and other substituted derivatives. Its rigid, fully conjugated structure also confers good thermal stability, an important characteristic for materials intended to withstand processing and prolonged illumination.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 9-fluorenone is typically encountered in university and institutional research settings where organic synthesis and materials chemistry overlap. It appears in postgraduate synthetic work as an intermediate toward fluorene-derived structures, and in photochemistry and photocatalysis studies that examine energy and electron transfer. Materials groups working on light-harvesting and organic electronic systems keep it as a reference acceptor, while teaching laboratories use it to demonstrate carbonyl reactivity within a rigid aromatic framework.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSynthetic building block: the reactive carbonyl and rigid fluorene core allow straightforward elaboration into alcohols, olefins, and substituted derivatives for multi-step organic synthesis programmes.\u003c\/li\u003e\n\u003cli\u003ePhotosensitizer in photochemical reactions: strong absorption of ultraviolet and visible light combined with a long-lived triplet excited state lets it transfer energy efficiently to substrate molecules.\u003c\/li\u003e\n\u003cli\u003eElectron acceptor studies: the conjugated carbonyl readily draws electrons from donor molecules, making it a useful probe for investigating photoinduced electron transfer processes.\u003c\/li\u003e\n\u003cli\u003eLight-conversion materials research: good thermal stability and extended conjugation suit it to materials laboratories developing systems that convert absorbed light into usable chemical or electrical energy.\u003c\/li\u003e\n\u003cli\u003eCarbonyl reactivity demonstrations: its distinct yellow colour and well-defined nucleophilic addition chemistry make it an instructive reagent for teaching and method-development work in organic chemistry.\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: F0021\u003c\/li\u003e\n\u003cli\u003eCAS number: 486-25-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePhysical form: solid, characteristically yellow in colour\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, protected from light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore 9-Fluorenone in its original tightly closed container in a cool, dry, well-ventilated area away from direct sunlight and other light sources, since the compound is photochemically active and should not be left exposed to illumination. Amber glass or otherwise light-protected containers are appropriate for any material transferred out of the original packaging. Handle the solid inside a fume hood to avoid inhaling dust, and wear a laboratory coat, safety goggles, and chemical-resistant gloves throughout. Keep the container away from strong oxidising agents and from sources of heat or ignition. Close the container promptly after use, label all transferred material clearly, and consult the manufacturer's safety data sheet before first use and before any disposal step.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48086974071002,"sku":"TCI2510F002129695","price":507000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086974103770,"sku":"TCI2510F002129696","price":1125000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086974136538,"sku":"TCI2510F002129697","price":3682000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F0021.jpg?v=1767113194"},{"product_id":"tci2510f124531374","title":"TCI F1245 922706-40-9 2-(9H-Fluoren-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-(9H-Fluoren-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is an organoboron compound widely used in chemical laboratories for its versatile reactivity in organic synthesis. This compound plays a crucial role in facilitating carbon-carbon bond formation, particularly in coupling reactions such as the Suzuki-Miyaura reaction. Its unique molecular structure allows it to act as a key reagent in the development of complex organic molecules, making it indispensable in modern synthetic chemistry. Due to its stability and reactivity, it is frequently employed in research settings where precise chemical transformations are required.\u003c\/p\u003e\n\u003cp\u003eThe compound’s organoboron nature contributes to its effectiveness in various synthetic pathways. Its dioxaborolane framework provides both structural stability and reactivity, enabling it to participate in a range of organometallic reactions. The presence of the fluorene group enhances its compatibility with aromatic halides, making it a preferred choice for coupling reactions. Additionally, its non-toxic profile and ease of degradation under certain conditions make it a safe and reliable option for laboratory use. These properties collectively ensure its widespread application in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, particularly in universities and research institutions. Its role in synthetic processes has made it a standard reagent in the development of new chemical compounds. The compound’s reliability and effectiveness have led to its adoption in various experimental setups, supporting the advancement of chemical research in Indonesia. Its availability and performance make it a preferred choice for researchers working on complex molecular synthesis.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSuzuki-Miyaura Coupling: This compound is ideal for coupling aromatic halides with boronic acids, enabling efficient carbon-carbon bond formation in organic synthesis.\u003c\/li\u003e\n\u003cli\u003eOrganic Synthesis Reactions: Its reactivity and stability make it a valuable reagent in the synthesis of complex organic molecules, supporting a wide range of chemical transformations.\u003c\/li\u003e\n\u003cli\u003eResearch and Development Projects: It is frequently used in R\u0026amp;D initiatives where precise and controlled chemical reactions are necessary for developing new compounds.\u003c\/li\u003e\n\u003cli\u003eAcademic Teaching Laboratories: Its role in synthetic chemistry makes it a common reagent in educational settings for teaching advanced organic reaction mechanisms.\u003c\/li\u003e\n\u003cli\u003eIndustrial Chemical Processes: Its reliability and performance in coupling reactions make it suitable for use in industrial applications requiring high chemical yield and 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: 922706-40-9\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 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 stability and reactivity. It is recommended to use airtight containers to prevent exposure to moisture, which can affect its chemical integrity. Due to its organoboron nature, it should be handled with care to avoid any potential reactions with incompatible substances. In laboratory settings, it is advisable to store it in a well-ventilated area and ensure that it is kept away from heat sources. Proper labeling and storage practices are essential to ensure safe handling and prevent accidental contamination. Always follow standard laboratory safety protocols when working with this compound to ensure a safe and efficient research environment.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48087070638298,"sku":"TCI2510F124531374","price":3008000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48087070671066,"sku":"TCI2510F124531375","price":10681000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510F1245.jpg?v=1769056190"},{"product_id":"tci2510h032932848","title":"TCI H0329 6949-73-1 2-Hydroxy-9-fluorenone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Hydroxy-9-fluorenone is a chemical compound widely used in laboratory settings for the synthesis of complex molecules. This compound serves as a key building block in organic chemistry, particularly in the development of heterocyclic compounds and other organic derivatives. Its unique molecular structure allows it to participate effectively in various chemical reactions, making it a valuable reagent for researchers. In the laboratory, it is commonly used as a reactant in substitution and oxidation reactions due to its reactivity and functional versatility.\u003c\/p\u003e\n\u003cp\u003eOne of the main reasons for its popularity is its solubility in organic solvents such as ethyl acetate and chloroform. This solubility characteristic simplifies its handling and integration into different reaction systems. Additionally, its stability under certain conditions ensures reliable performance in experimental processes. These properties contribute to its efficiency in chemical synthesis, enabling researchers to achieve consistent and reproducible results.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, 2-Hydroxy-9-fluorenone plays a crucial role in both fundamental and applied chemical research. It is frequently used in the development of new compounds and in the study of molecular reactivity. Many research institutions and universities in Indonesia rely on this compound for its versatility and effectiveness in various synthetic processes, supporting advancements in pharmaceutical and industrial chemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSynthesis of heterocyclic compounds for drug development due to its reactivity and structural versatility.\u003c\/li\u003e\n\u003cli\u003eAromatic substitution reactions in the creation of functionalized organic molecules because of its stability and solubility.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research in Indonesian academic institutions for the study of molecular reactivity and synthetic pathways.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical synthesis applications where reliable and efficient reagents are required for complex molecule production.\u003c\/li\u003e\n\u003cli\u003eDevelopment of new pharmaceutical compounds through controlled chemical reactions that benefit from its unique molecular structure.\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: 6949-73-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Building Blocks \u0026gt; Non-Heterocyclic Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various sizes as per standard laboratory supply\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or crystalline, depending on the specific product\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from direct sunlight and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003e2-Hydroxy-9-fluorenone should be stored in a cool, dry environment to maintain its chemical integrity. It is recommended to keep it in a tightly sealed container to prevent exposure to moisture and air. Due to its reactivity, it should be handled in a well-ventilated area, ideally with appropriate personal protective equipment. Avoid contact with incompatible materials such as strong oxidizing agents. Regular monitoring of storage conditions is essential to ensure the compound remains stable and effective for use in laboratory applications. 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