{"title":"Chemicals by Class › 6-Membered Carbocyclic Compounds","description":"\u003cp\u003e6-membered carbocyclic compounds from TCI: substituted benzenes, cyclohexane, naphthalene, anthracene, pyrene, perylene, fluorene, adamantane — the most widely used basic frameworks in organic synthesis. Official TCI distributor in Indonesia: AMI Scientific.\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":2474000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5521_28642260-58c4-44fe-a6ed-4e27de281cb3.jpg?v=1792630664"},{"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":3558000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5580_98636e51-1447-4048-81be-32d295ffb6d5.jpg?v=1792630719"},{"product_id":"tci2510b559512269","title":"TCI B5595 711-02-4 Bicyclo[2.2.2]octane-1,4-dicarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5595 Bicyclo[2.2.2]octane-1,4-dicarboxylic Acid (CAS 711-02-4) is a rigid cage-structured dicarboxylic acid used as a non-heterocyclic building block in organic synthesis. This compound serves as a versatile precursor for constructing Metal-Organic Frameworks (MOFs), coordination polymers, and functional porous materials that require high structural rigidity. Its well-defined geometry also makes it suitable for supramolecular chemistry and catalyst design applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085889908954,"sku":"TCI2510B559512269","price":4721000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5595_266ea02a-4191-4ab0-939c-2e0fbe571885.jpg?v=1792630737"},{"product_id":"tci2510b561312299","title":"TCI B5613 138124-32-0 (R,R)-(-)-N,N'-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminomanganese(III) Chloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5613, commercially known as Jacobsen's catalyst, is a chiral manganese(III)-salen complex widely employed for highly enantioselective epoxidation of unfunctionalized alkenes. It is also utilized in asymmetric ring-opening reactions, enantioselective sulfide oxidation, and various other stereoselective transformations critical in medicinal chemistry and natural product synthesis. This compound is an essential tool for research laboratories focused on asymmetric catalysis and chiral building block preparation.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48276771274970,"sku":"TCI2510B561312299","price":3029000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5613_37968e01-a0bb-4eb4-8901-0f6e333ded85.jpg?v=1792630757"},{"product_id":"tci2510b561512301","title":"TCI B5615 1086641-47-5 9-(3-Bromophenyl)-9H-fluoren-9-ol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5615 9-(3-Bromophenyl)-9H-fluoren-9-ol is a bromine-substituted fluorene derivative that serves as a non-heterocyclic building block in organic synthesis. This compound is widely used as a precursor for constructing more complex molecular architectures through coupling and further functionalization reactions. It is particularly valuable in the development of functional organic materials, including organic light-emitting materials and organic semiconductors, as well as in medicinal chemistry research for drug candidate development.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085891088602,"sku":"TCI2510B561512301","price":1263000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085891121370,"sku":"TCI2510B561512302","price":4442000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5615.jpg?v=1768815835"},{"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":2171000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085891350746,"sku":"TCI2510B561712306","price":7471000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5617.jpg?v=1768815838"},{"product_id":"tci2510b564712345","title":"TCI B5647 146504-07-6 (1R,2R)-N1-(tert-Butoxycarbonyl)-1,2-cyclohexanediamine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(1R,2R)-N1-(tert-Butoxycarbonyl)-1,2-cyclohexanediamine (TCI B5647) is a chiral building block widely used in asymmetric synthesis, featuring a Boc-protected primary amine that allows selective functionalization of the secondary amine position. This compound is particularly valuable for the preparation of chiral catalysts, enantioselective ligands, and pharmaceutical intermediates requiring high enantiomeric purity. With its well-defined (1R,2R) stereochemistry, it serves as a reliable scaffold in medicinal chemistry research, drug development, and total synthesis of natural products.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":67556232036570,"sku":"TCI2510B564712345","price":3257000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5647.jpg?v=1792630773"},{"product_id":"tci2510b564812347","title":"TCI B5648 180683-64-1 (1S,2S)-N1-(tert-Butoxycarbonyl)-1,2-cyclohexanediamine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(1S,2S)-N1-(tert-Butoxycarbonyl)-1,2-cyclohexanediamine (CAS 180683-64-1) is a chiral building block widely employed in asymmetric synthesis, featuring a free primary amine and a Boc-protected amine for selective functionalization. This compound serves as a key precursor for the construction of chiral ligands, organocatalysts, and enantiopure intermediates in medicinal chemistry and total synthesis. Manufactured by TCI, it is available in 1 g and 5 g pack sizes to accommodate both exploratory and scale-up laboratory needs.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085894103258,"sku":"TCI2510B564812347","price":2726000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085894136026,"sku":"TCI2510B564812348","price":9313000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5648_5d8a6494-f2a2-4284-b660-d3394111de6a.jpg?v=1792630776"},{"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":3634000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5656_fe345dd2-3d88-44da-8e89-40856cda3f95.jpg?v=1792630783"},{"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":4039000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5673_91e345b4-1b35-4c02-b490-bad300b1ddfd.jpg?v=1792630796"},{"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":1642000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5678.jpg?v=1768815858"},{"product_id":"tci2510b571712438","title":"TCI B5717 323195-31-9 9-([1,1'-Biphenyl]-4-yl)anthracene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5717 9-([1,1'-Biphenyl]-4-yl)anthracene (CAS 323195-31-9) is a high-purity small molecule semiconductor building block designed for advanced materials research. It is commonly employed as a precursor in the synthesis of organic semiconductors for applications such as OLEDs, OFETs, and organic photovoltaic devices. Its biphenyl-anthracene framework provides favorable optoelectronic properties and charge transport characteristics for next-generation organic electronics.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085899018458,"sku":"TCI2510B571712438","price":1162000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085899051226,"sku":"TCI2510B571712439","price":3963000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5717.jpg?v=1768815871"},{"product_id":"tci2510b573212458","title":"TCI B5732 176763-62-5 (R,R)-N,N'-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(R,R)-N,N'-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II) is a cobalt(II) salen complex commonly referred to as a Jacobsen-type catalyst, widely employed in C–H activation reactions and asymmetric catalysis. This chiral catalyst facilitates direct functionalization of unactivated carbon–hydrogen bonds and is also effective in enantioselective epoxidation and epoxide ring-opening reactions. It is a valuable reagent for synthetic organic chemistry laboratories working on pharmaceutical intermediates and fine chemical synthesis.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085899837658,"sku":"TCI2510B573212458","price":1641000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085899870426,"sku":"TCI2510B573212459","price":5982000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5732.jpg?v=1792630843"},{"product_id":"tci2510b573712464","title":"TCI B5737 6751-75-3 2-Bromoresorcinol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Bromoresorcinol (CAS 6751-75-3) is a brominated resorcinol derivative widely employed as a non-heterocyclic building block in organic synthesis. This compound serves as a key intermediate for constructing pharmaceuticals, agrochemicals, and advanced materials, with the bromine atom enabling further cross-coupling reactions. Its dual hydroxyl groups and ortho-bromine substitution make it a versatile precursor for ligands, catalysts, and biologically active molecular frameworks.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085900099802,"sku":"TCI2510B573712464","price":884000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085900132570,"sku":"TCI2510B573712465","price":2903000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5737.jpg?v=1768815876"},{"product_id":"tci2510b575612489","title":"TCI B5756 846-20-8 2-Bromonaphthalene-1,4,5,8-tetracarboxylic 1,8:4,5-Dianhydride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Bromonaphthalene-1,4,5,8-tetracarboxylic 1,8:4,5-Dianhydride is a complex chemical compound widely used in materials science research. It plays a crucial role in the development of advanced materials, particularly in the synthesis of semiconductors and conductive polymers. This compound is essential for creating molecular structures with unique electronic and optical properties, making it a valuable resource in modern laboratory settings. Its versatility allows it to be integrated into various synthetic pathways, supporting innovation in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eThe compound is favored for its stable chemical structure and its ability to undergo highly specific chemical reactions. Its anhydride functionality enables efficient polymerization and molecular modification processes, which are critical for developing new materials with tailored properties. The compound’s solubility in organic solvents further enhances its usability in laboratory synthesis, ensuring ease of handling and integration into complex reaction schemes. These properties make it a preferred choice for researchers aiming to design advanced materials with precise functional characteristics.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in semiconductor material research, conductive polymer development, and the creation of advanced composite materials. Its role is vital in supporting scientific innovation across various academic and research institutions in Indonesia. The compound’s reliability and performance contribute to the advancement of material science in the region, making it a key component in cutting-edge research projects.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSemiconductor material synthesis due to its ability to form stable molecular structures with unique electronic properties.\u003c\/li\u003e\n\u003cli\u003eConductive polymer development as it enables efficient polymerization and molecular modification processes.\u003c\/li\u003e\n\u003cli\u003eAdvanced composite material creation because of its compatibility with various organic solvents and chemical reactivity.\u003c\/li\u003e\n\u003cli\u003eOptical material research due to its potential for tuning electronic and optical characteristics in synthetic pathways.\u003c\/li\u003e\n\u003cli\u003eMolecular engineering applications where precise chemical reactions and structural modifications are required.\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: 846-20-8\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, crystalline appearance\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to use airtight containers to prevent exposure to moisture and air, which could affect its reactivity. Due to its chemical nature, it should be handled in a well-ventilated laboratory setting to ensure safety. Avoid contact with incompatible materials such as strong acids or bases. Always use appropriate personal protective equipment, including gloves and safety goggles, when handling this compound. Proper storage and handling are essential to preserve its integrity and ensure safe laboratory operations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085901017306,"sku":"TCI2510B575612489","price":5048000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085901050074,"sku":"TCI2510B575612490","price":17641000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5756.jpg?v=1768815883"},{"product_id":"tci2510b577012507","title":"TCI B5770 1416243-42-9 2-[10-([1,1'-Biphenyl]-4-yl)anthracen-9-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5770 is an organoboron reagent featuring a dioxaborolane functional group coupled with a biphenyl-anthracene scaffold, primarily utilized in Suzuki-Miyaura cross-coupling reactions for constructing complex aromatic molecular architectures. This compound serves as a valuable building block in the synthesis of optoelectronic materials, including OLED emitters and organic semiconductors, owing to the favorable photophysical properties of its anthracene core. It is also widely employed in medicinal chemistry research for the preparation of substituted aromatic compound libraries with potential pharmaceutical applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085901902042,"sku":"TCI2510B577012507","price":3736000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5770_7a936e6f-5de1-46b5-8594-919c7e48662a.jpg?v=1792630867"},{"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":1237000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5842.jpg?v=1792630936"},{"product_id":"tci2510b589712667","title":"TCI B5897 867374-53-6 2-Bromo-7-iodo-9H-fluoren-9-one","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5897, 2-Bromo-7-iodo-9H-fluoren-9-one (CAS 867374-53-6), is a non-heterocyclic building block featuring dual halogen functional groups at the 2- and 7-positions of the fluorenone core, making it a valuable intermediate for palladium-catalyzed cross-coupling reactions such as Suzuki and Sonogashira couplings. This compound is widely employed in the synthesis of organic electronic materials including OLED emitters and organic semiconductors. It also serves as a key precursor in medicinal chemistry for constructing diverse molecular libraries through selective halogen substitution.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085908816090,"sku":"TCI2510B589712667","price":1970000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085908848858,"sku":"TCI2510B589712668","price":6689000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5897.jpg?v=1792631000"},{"product_id":"tci2510b595412733","title":"TCI B5954 117901-97-0 N,N'-Bis[3-(dimethylamino)propyl]perylene-3,4,9,10-tetracarboxylic Diimide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5954 N,N'-Bis[3-(dimethylamino)propyl]perylene-3,4,9,10-tetracarboxylic Diimide is a perylene diimide derivative widely utilized as an n-type organic semiconductor in the fabrication of Organic Field-Effect Transistors (OFETs). This compound exhibits favorable electron mobility and excellent thermal and photochemical stability, making it suitable for flexible and printed electronic device research. Its applications also extend to organic photovoltaic cells (OPV), organic light-emitting diodes (OLED), and optoelectronic sensor development.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085911437530,"sku":"TCI2510B595412733","price":3332000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085911470298,"sku":"TCI2510B595412734","price":11635000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5954.jpg?v=1768815937"},{"product_id":"tci2510b596712749","title":"TCI B5967 1477458-14-2 2'-Bromospiro[fluorene-9,9'-xanthene]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5967 2'-Bromospiro[fluorene-9,9'-xanthene] (CAS 1477458-14-2) is a heterocyclic building block featuring a spiro-linked fluorene-xanthene core with a reactive bromo substituent at the 2' position. This compound serves as a versatile intermediate in cross-coupling reactions, including Suzuki, Stille, and Buchwald-Hartwig couplings, enabling the synthesis of more complex molecular architectures. It is widely utilized in materials science research for developing organic electronic materials such as OLED emitters and organic semiconductors, as well as in medicinal chemistry for constructing rigid, thermally stable molecular scaffolds.\u003c\/p\u003e\n\u003cp\u003e---\u003c\/p\u003e\n\u003cp\u003e*Asumsi: Kondisi penyimpanan standar untuk senyawa organik spiro berbasis rekomendasi umum TCI.*\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48276769538266,"sku":"TCI2510B596712749","price":2852000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5967.jpg?v=1792631046"},{"product_id":"tci2510b600612794","title":"TCI B6006 950779-13-2 1,6-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,6-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyrene is a highly specialized organoboron compound used in advanced chemical research. This compound plays a crucial role in synthetic chemistry, particularly in the development of complex molecular structures. Its unique structure, featuring boron-containing groups, makes it an essential reagent in various coupling reactions, such as Suzuki-Miyaura and Kumada-Corriu. Due to its reactivity and versatility, it is widely utilized in laboratories for creating aromatic compounds with specific functional groups.\u003c\/p\u003e\n\u003cp\u003eThe compound's organoboron functionality provides it with exceptional reactivity towards transition metals and organic compounds. This reactivity allows it to participate in a wide range of chemical transformations, making it a preferred choice for synthetic chemists. Its ability to form stable intermediates under controlled conditions enhances its utility in multi-step synthesis processes. The presence of the boron group also contributes to its stability in certain environments, which is vital for maintaining the integrity of the reaction pathway.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in the synthesis of aromatic compounds and drug development. Its availability in the local market ensures that researchers have access to high-quality reagents for their experiments. The compound is a valuable tool for those working on complex molecular structures and functional group modifications. Its application is particularly relevant in academic and industrial research settings where precision and reliability are essential.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eOrganic synthesis of aromatic compounds with specific substituents due to its reactivity and compatibility with coupling reactions.\u003c\/li\u003e\n\u003cli\u003eDevelopment of pharmaceutical compounds through the formation of complex molecular frameworks using boron-based intermediates.\u003c\/li\u003e\n\u003cli\u003eResearch in transition metal catalysis where the compound serves as a versatile coupling agent in various synthetic pathways.\u003c\/li\u003e\n\u003cli\u003ePreparation of functionalized pyrene derivatives for use in materials science and photonic applications.\u003c\/li\u003e\n\u003cli\u003eInvestigation of boron-based reaction mechanisms in both academic and industrial research environments.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 950779-13-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Organometallic Reagents \u0026gt; Organoboron [Organometallic Reagents]\u003c\/li\u003e\n\u003cli\u003ePack sizes: 1 g, 5 g, 25 g\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and light exposure. Due to its reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure proper ventilation in the laboratory when working with this material. Avoid contact with incompatible substances to prevent unwanted chemical reactions. Proper storage and handling practices are essential to ensure the safety of laboratory personnel and the integrity of the compound.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085914386650,"sku":"TCI2510B600612794","price":4518000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085914419418,"sku":"TCI2510B600612795","price":15143000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6006_4e175022-1e27-4cf1-9e73-50bda2773f2e.jpg?v=1792631085"},{"product_id":"tci2510b603712841","title":"TCI B6037 13292-05-2 3-Bromophenanthrene-9,10-dione","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e3-Bromophenanthrene-9,10-dione is a non-heterocyclic building block widely utilized as a key intermediate in the synthesis of substituted phenanthrene derivatives. It serves as a versatile precursor for cross-coupling reactions, selective oxidations, and further functional group modifications aimed at constructing complex molecular architectures. This compound finds applications in the development of functional organic materials, including dyes, fluorescent sensors, and organic semiconductors, owing to the dual reactivity conferred by its quinone moiety and bromo substituent.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085916254426,"sku":"TCI2510B603712841","price":1389000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085916287194,"sku":"TCI2510B603712842","price":4695000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6037.jpg?v=1792631122"},{"product_id":"tci2510b610312920","title":"TCI B6103 3401-47-6 1-Bromo-2-methoxynaphthalene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-Bromo-2-methoxynaphthalene (CAS 3401-47-6) is a naphthalene-based building block featuring bromo and methoxy substituents, widely utilized in organic synthesis laboratories. It serves as a key intermediate for cross-coupling reactions including Suzuki-Miyaura and Ullmann couplings, enabling the construction of carbon-carbon and carbon-heteroatom bonds on the naphthalene scaffold. This compound is commonly applied in medicinal chemistry research, functional organic material development, and the synthesis of polycyclic aromatic derivatives.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085920153818,"sku":"TCI2510B610312920","price":1187000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085920186586,"sku":"TCI2510B610312921","price":4065000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6103.jpg?v=1768815981"},{"product_id":"tci2510b610712926","title":"TCI B6107 162558-25-0 (S)-3-(tert-Butoxycarbonylamino)-2-[(9H-fluoren-9-ylmethoxy)carbonylamino]propionic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eThis compound is a doubly protected amino acid derivative featuring Fmoc and Boc orthogonal protecting groups, widely used as a versatile building block in solid-phase peptide synthesis (SPPS). It enables selective deprotection and stepwise modification of diaminopropionic acid residues in complex peptide chains. Common applications include the development of modified peptides, bioactive peptidomimetics, and molecular probes for biochemical and medicinal chemistry research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085920383194,"sku":"TCI2510B610712926","price":2247000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085920415962,"sku":"TCI2510B610712927","price":7622000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6107.jpg?v=1768815983"},{"product_id":"tci2510b611412933","title":"TCI B6114 937372-45-7 4-(10-Bromoanthracen-9-yl)benzonitrile","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6114 4-(10-Bromoanthracen-9-yl)benzonitrile is a high-purity small molecule building block designed for the synthesis of organic semiconductor materials used in advanced optoelectronic research. Featuring a bromo-substituted anthracene core with a benzonitrile functional group, this compound serves as a versatile precursor for fabricating OLEDs, OFETs, and organic photovoltaic devices. Its unique electronic properties also make it suitable for developing fluorescent materials, emissive layers, and fluorescence-based sensing platforms in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085920645338,"sku":"TCI2510B611412933","price":3307000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6114.jpg?v=1768815984"},{"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":1742000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085921235162,"sku":"TCI2510B612812948","price":6082000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6128.jpg?v=1792631220"},{"product_id":"tci2510b614712970","title":"TCI B6147 5467-58-3 1-Bromo-4-methoxynaphthalene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1-Bromo-4-methoxynaphthalene (CAS 5467-58-3) is a naphthalene-based organic building block commonly employed in cross-coupling reactions such as Suzuki-Miyaura, Heck, and Buchwald-Hartwig couplings for the construction of complex aromatic frameworks. This TCI product serves as a versatile precursor in medicinal chemistry research, advanced organic synthesis, and the development of naphthalene-derived bioactive compounds and functional materials.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085922054362,"sku":"TCI2510B614712970","price":1944000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085922087130,"sku":"TCI2510B614712971","price":6739000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6147-struktur.jpg?v=1791524946"},{"product_id":"tci2510b614912974","title":"TCI B6149 822-85-5 2-Bromocyclohexan-1-one (stabilized with HQ + CaCO3)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6149 2-Bromocyclohexan-1-one is a brominated cyclic ketone widely used as a non-heterocyclic building block in organic synthesis. Stabilized with hydroquinone (HQ) and calcium carbonate (CaCO₃) to ensure long-term purity and reactivity, this compound serves as a key intermediate for constructing heterocyclic scaffolds, pharmaceutical candidates, and agrochemical precursors. Its alpha-brominated carbonyl structure makes it a versatile electrophile suitable for nucleophilic substitution, cross-coupling, and various carbon-carbon bond-forming reactions in research and development settings.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48085922185434,"sku":"TCI2510B614912974","price":960000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085922218202,"sku":"TCI2510B614912975","price":2752000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6149.jpg?v=1792631236"},{"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":4065000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6180_f267c57d-5009-40d8-bf79-9e3d9890087f.jpg?v=1792631273"},{"product_id":"tci2510b619813022","title":"TCI B6198 2754-40-7 Bicyclo[2.2.2]octane-2,3,5,6-tetracarboxylic 2,3:5,6-Dianhydride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBicyclo[2.2.2]octane-2,3,5,6-tetracarboxylic 2,3:5,6-Dianhydride (CAS 2754-40-7) is a bicyclic dianhydride monomer designed for the synthesis of high-performance polyimides and specialty polymers. Its rigid bicyclo[2.2.2]octane framework imparts excellent thermal stability and mechanical strength to the resulting polymeric materials. This reagent is widely applied in advanced material research, including gas separation membranes, optoelectronic components, and heat-resistant coatings for aerospace and electronics industries.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085924184282,"sku":"TCI2510B619813022","price":2853000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085924217050,"sku":"TCI2510B619813023","price":9943000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6198.jpg?v=1768816002"},{"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":1289000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085925232858,"sku":"TCI2510B622313052","price":4518000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6223.jpg?v=1768816008"},{"product_id":"tci2510b639013269","title":"TCI B6390 (1S,2S)-N~1~,N~2~-Dibenzylcyclohexane-1,2-diamine Dihydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6390 is (1S,2S)-N1,N2-dibenzylcyclohexane-1,2-diamine dihydrochloride (CAS 3070821-54-1), a chiral building block based on the widely used trans-1,2-diaminocyclohexane scaffold. Its C2-symmetric, enantiodefined framework underpins many chiral ligands and bifunctional organocatalysts, including salen-type ligands and thiourea or squaramide catalysts. The dihydrochloride salt form improves handling and shelf stability relative to the free base, which can be liberated immediately before use. Available in 1 g and 5 g packs, it should be kept tightly closed in a cool, dry place because amine salts readily take up moisture.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085937586394,"sku":"TCI2604B639040","price":3484000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085937619162,"sku":"TCI2604B639041","price":13375000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6390.jpg?v=1792631469"},{"product_id":"tci2510b639313272","title":"TCI B6393 212611-88-6 (1R,2R)-N1,N2-Dibenzylcyclohexane-1,2-diamine Dihydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6393 is (1R,2R)-N1,N2-dibenzylcyclohexane-1,2-diamine dihydrochloride (CAS 212611-88-6), the enantiomeric counterpart within this chiral building block series. Built on the rigid, C2-symmetric trans-1,2-diaminocyclohexane scaffold, it is a versatile precursor to chiral diamine ligands and bifunctional thiourea or squaramide organocatalysts. Having both enantiomers available lets researchers switch the sense of asymmetric induction simply by changing the chirality source. Supplied in 1 g and 5 g packs, the hygroscopic salt should be stored cool, dry, and tightly sealed, with the free base generated shortly before use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085937717466,"sku":"TCI2510B639313272","price":3484000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085937750234,"sku":"TCI2510B639313273","price":13553000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6393.jpg?v=1792631471"},{"product_id":"tci2510b641713303","title":"TCI B6417 464-43-7 (+)-Borneol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6417 (+)-Borneol (CAS 464-43-7) is a bicyclic monoterpene alcohol supplied as a crude medicine ingredient intended for research and experimental use. It is commonly employed as a reference compound in phytochemical studies and in the characterisation of plant-derived extracts. The single-enantiomer form also makes it useful for stereochemistry-oriented investigations and for the synthesis of bornyl derivatives. Store the material in a tightly closed container in a cool, dry place away from light, and always consult the manufacturer's safety data sheet before handling.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eMa et al. (2023). Comparison of pharmacological activity and safety of different stereochemical configurations of borneol: L-borneol, D-borneol, and synthetic borneol. \u003cem\u003eBiomedicine \u0026amp; Pharmacotherapy\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.biopha.2023.114668\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.biopha.2023.114668\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e(2016). Preparation of borneol loaded hollow mesoporous silica nanoparticles and effect on borneol volatility. \u003cem\u003eChina Journal of Chinese Materia Medica\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.4268\/cjcmm20161510\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.4268\/cjcmm20161510\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMa et al. (2017). Microcalorimetric study of the effect of l-borneol, d-borneol and synthetic borneol on the growth of P. aeruginosa. \u003cem\u003eJournal of Thermal Analysis and Calorimetry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s10973-017-6627-3\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s10973-017-6627-3\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085939028186,"sku":"TCI2510B641713303","price":1112000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085939060954,"sku":"TCI2510B641713304","price":3710000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6417_ee0c7381-239a-4096-8e7f-009320e254dd.jpg?v=1792631508"},{"product_id":"tci2510b643713325","title":"TCI B6437 115951-16-1 1-[(tert-Butoxycarbonyl)amino]cyclohexanecarboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6437 1-[(tert-Butoxycarbonyl)amino]cyclohexanecarboxylic Acid (CAS 115951-16-1) is a Boc-protected cyclic amino acid in which the amino and carboxyl groups share a quaternary carbon. Its rigid cyclohexane framework makes it valuable for designing conformationally constrained peptides and peptide analogues. The pre-installed Boc group saves a protection step and can be removed under well-established acidic conditions. Store the solid tightly sealed in a cool, dry place away from strong acids, and refer to the manufacturer's safety data sheet before handling.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBadland et al. (2010). An improved synthesis of (1R,3S)-3-[(tert-butoxycarbonyl)amino]cyclohexanecarboxylic acid. \u003cem\u003eTetrahedron: Asymmetry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.tetasy.2010.04.049\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.tetasy.2010.04.049\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKadyrov et al. (2021). Convenient Synthesis of (R)-3-[(tert-Butoxycarbonyl)amino]piperidine and (R)-3-[(tert-Butoxycarbonyl)amino]azepane. \u003cem\u003eSynthesis\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/a-1526-7657\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/a-1526-7657\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e(2012). Discussion Addendum For: Efficient Asymmetric Synthesis of N-tert-Butoxycarbonyl a-Amino Acids using 4-tert-Butoxycarbonyl-5,6-Diphenylmorpholin-2-one:. \u003cem\u003eOrganic Syntheses\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.15227\/orgsyn.089.0394\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.15227\/orgsyn.089.0394\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085939912922,"sku":"TCI2510B643713325","price":1792000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085939945690,"sku":"TCI2510B643713326","price":6132000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6437.jpg?v=1792631539"},{"product_id":"tci2510b654113466","title":"TCI B6541 195-19-7 Benzo[c]phenanthrene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBenzo[c]phenanthrene (CAS 195-19-7) is a four-ring polycyclic aromatic hydrocarbon whose angular ring arrangement creates a characteristic fjord region and slight molecular twist. It is widely used as a research reference material in PAH analysis, environmental chemistry studies, photochemistry, and the synthesis of helicenes and other non-planar aromatics. The compound should be handled in a fume hood with appropriate personal protective equipment, kept dry, and protected from light. AMI Scientific supplies it in 200 mg and 1 g pack sizes strictly for laboratory research use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085946171610,"sku":"TCI2510B654113466","price":1742000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085946204378,"sku":"TCI2510B654113467","price":5982000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6541_2a653afc-5ec8-4a50-a2ea-17ca16786c69.jpg?v=1792631651"},{"product_id":"tci2510b655213480","title":"TCI B6552 2763205-15-6 2',7'-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)spiro[cyclopenta[2,1-b:3,4-b']dipyridine-5,9'-fluorene]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6552 is a spiro-linked building block bearing two pinacol boronate groups at the 2' and 7' positions of a spiro[cyclopenta-dipyridine-fluorene] framework. Its difunctional boronate handles make it a convenient monomer for palladium-catalysed Suzuki–Miyaura cross-coupling and for the assembly of conjugated oligomers and polymers. The rigid, orthogonal spiro geometry combined with electron-poor pyridine nitrogens is of particular interest in organic optoelectronic material research and in nitrogen-donor ligand design. AMI Scientific supplies this TCI product in 100 mg and 500 mg pack sizes; always consult the official TCI documentation and safety data sheet before use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48085946859738,"sku":"TCI2510B655213480","price":2020000.0,"currency_code":"IDR","in_stock":true},{"title":"500mg","offer_id":48085946892506,"sku":"TCI2510B655213481","price":6890000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6552_2f2f4c5c-80a2-4de2-8583-9ea22d2ceb26.jpg?v=1792631678"},{"product_id":"tci2510b660613561","title":"TCI B6606 2897656-97-0 N1-([1,1'-Biphenyl]-2-yl)-N2-(2-phenylnaphthalen-1-yl)benzene-1,2-diamine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6606 is a sterically demanding N,N'-diaryl benzene-1,2-diamine bearing biphenyl-2-yl and 2-phenylnaphthalen-1-yl substituents. Such o-phenylenediamine frameworks are commonly used as precursors to benzimidazolium salts and N-heterocyclic carbene ligands for organometallic catalysis. The bulky aryl groups create a well-defined steric pocket that can influence catalytic selectivity, and the scaffold is also of interest in functional organic materials. AMI Scientific offers this TCI building block in 250 mg and 1 g pack sizes for catalysis and materials research laboratories.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48085950005466,"sku":"TCI2510B660613561","price":1994000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085950038234,"sku":"TCI2510B660613562","price":5805000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6606_27dc89e2-2b2f-459a-abd7-7c4c2829d91a.jpg?v=1792631744"},{"product_id":"tci2510b663813598","title":"TCI B6638 694-98-4 Bicyclo[2.2.1]hept-5-en-2-one","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6638 Bicyclo[2.2.1]hept-5-en-2-one (CAS 694-98-4), commonly known as norbornenone, is a strained bicyclic enone available from AMI Scientific. The strained alkene drives efficient ring-opening metathesis polymerisation and Diels-Alder chemistry, while the ketone group supports reduction, organometallic addition, and Baeyer-Villiger oxidation. Its rigid framework also makes it valuable for stereoselective synthesis and terpenoid-type scaffold construction. Offered in 200 mg and 1 g packs, it should be stored cold, sealed, and protected from light to prevent unwanted polymerisation.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"200mg","offer_id":48085951480026,"sku":"TCI2510B663813598","price":1363000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085951512794,"sku":"TCI2510B663813599","price":4594000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6638_6f1eef0d-0e57-453b-91b6-a0b23a74e085.jpg?v=1792631784"},{"product_id":"tci2510b696013841","title":"TCI B6960 1621397-55-4 3'-Bromospiro[fluorene-9,9'-xanthene]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6960 is 3'-bromospiro[fluorene-9,9'-xanthene], a spiro-linked building block in which fluorene and xanthene units are joined through a shared quaternary carbon. The near-orthogonal geometry interrupts conjugation between the two units and yields bulky, thermally robust, amorphous-favouring molecules. The bromine substituent offers a single well-defined site for Suzuki–Miyaura or Buchwald–Hartwig functionalisation. AMI Scientific supplies this TCI material in a 1 g pack; store it tightly closed in a cool, dry, light-protected place.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085962522842,"sku":"TCI2510B696013841","price":3458000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6960_7650ba25-f746-4ddd-afe4-c95b3dd2f4c5.jpg?v=1792631942"},{"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":1489000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48085963243738,"sku":"TCI2510B698113858","price":4997000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/tci2510b698113857-struktur-1000.png?v=1792629793"},{"product_id":"tci2510b698413859","title":"TCI B6984 2378498-93-0 7-Bromo-2,12-di-tert-butyl-5,9-dioxa-13b-boranaphtho[3,2,1-de]anthracene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6984 7-Bromo-2,12-di-tert-butyl-5,9-dioxa-13b-boranaphtho[3,2,1-de]anthracene (CAS 2378498-93-0) is a brominated boron–oxygen fused polycyclic building block used in advanced materials chemistry. The rigid, planar boron-containing framework is a well-known motif in the development of narrowband multi-resonance emitters. Its bromo handle enables palladium-catalysed cross-coupling and amination to install tailored donor or acceptor units. AMI Scientific supplies this organoboron reagent in a 250 mg research-scale pack for Indonesian laboratories.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"250mg","offer_id":48085963309274,"sku":"TCI2510B698413859","price":3686000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/tci2510b698413859-struktur-1000.png?v=1792629795"},{"product_id":"tci2510b699113862","title":"TCI B6991 20191-75-7 1-Bromonaphthalen-2-amine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6991 1-Bromonaphthalen-2-amine (CAS 20191-75-7) is a bifunctional naphthalene building block bearing adjacent bromo and amino groups. This ortho arrangement makes it a convenient precursor for annulation routes toward fused heterocycles, as well as for palladium-catalysed cross-coupling and diazonium chemistry. The naphthalene core is also valued in dye, ligand, and fluorescent materials research. AMI Scientific offers this reagent in 1 g and 5 g pack sizes for synthetic laboratories in Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085963407578,"sku":"TCI2510B699113862","price":1818000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085963440346,"sku":"TCI2510B699113863","price":6310000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/tci2510b699113862-struktur-1000.png?v=1792629797"},{"product_id":"tci2510c001013918","title":"TCI C0010 464-49-3 (+)-Camphor","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0010 (+)-Camphor, CAS 464-49-3, is an enantiomerically defined bicyclic ketone widely used as a chiral pool starting material. Its rigid bornane framework provides a reliable steric environment for asymmetric induction, making it valuable for preparing chiral auxiliaries, ligands, and resolving agents. The reactive C-2 ketone allows straightforward conversion into oximes, imines, alcohols, and other functionalised derivatives. AMI Scientific supplies this TCI product in 25 g and 500 g pack sizes for both method development and routine synthetic work.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003e(2016). Camphor. \u003cem\u003eReactions Weekly\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s40278-016-16081-z\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s40278-016-16081-z\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSahana et al. (2012). Camphor poisoning. \u003cem\u003eIndian Pediatrics\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s13312-012-0174-6\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s13312-012-0174-6\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMONEY (1996). ChemInform Abstract: Remote Functionalization of Camphor: Application to Natural Product Synthesis. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199649291\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199649291\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085965701338,"sku":"TCI2510C001013918","price":505000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085965734106,"sku":"TCI2510C001013919","price":2323000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0010_d12ca12a-d097-4435-bf40-f058e12413b3.jpg?v=1792631972"},{"product_id":"tci2510c001113920","title":"TCI C0011 76-22-2 (+\/-)-Camphor","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0011 (+\/-)-Camphor, CAS 76-22-2, is the racemic form of the well-known bicyclic terpenoid ketone. It is intended for applications where optical purity is not required, serving as an economical non-heterocyclic building block for general synthetic work. The reactive carbonyl group readily undergoes reduction, oximation, and condensation reactions, while its ready sublimation makes it a classic teaching material. AMI Scientific provides this TCI product in 25 g and 500 g pack sizes for research and teaching laboratories alike.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eChan et al. (2009). Status epilepticus after topical application of a solution containing camphor. \u003cem\u003eEmergency Medicine Journal\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1136\/emj.2008.063198\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1136\/emj.2008.063198\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eYE et al. (1991). ChemInform Abstract: Selective Anodic Oxidation of Camphor.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199142265\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199142265\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSTINSON (1998). Chiral camphor carries acetate in asymmetric condensation. \u003cem\u003eChemical \u0026amp; Engineering News Archive\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/cen-v076n005.p029\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/cen-v076n005.p029\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085965799642,"sku":"TCI2510C001113920","price":505000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085965832410,"sku":"TCI2510C001113921","price":1716000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0011_cb3e79c9-b135-46ce-976d-0c5910405e50.jpg?v=1792631975"},{"product_id":"tci2510c001213922","title":"TCI C0012 124-83-4 (+)-Camphoric Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0012 (+)-Camphoric Acid, CAS 124-83-4, is an optically active dicarboxylic acid derived from the camphor skeleton. Its two carboxyl groups and rigid carbon framework make it a practical chiral building block for asymmetric synthesis. The compound is commonly employed as a resolving agent for racemic bases and as a precursor to chiral ligands, esters, and amides. AMI Scientific offers this TCI product in 25 g and 100 g pack sizes for flexible laboratory use.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBaur et al. (2000). Quantitation and validation of cis-camphoric acid 3-methyl ester and cis-camphoric acid 1-methyl ester using CE. \u003cem\u003eJournal of Pharmaceutical and Biomedical Analysis\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0731-7085(99)00313-1\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0731-7085(99)00313-1\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eDmowski et al. (1997). Selective fluorination of (1R,3S)-(+)-camphoric acid with sulphur tetrafluoride. Preparation of fluorinated optically active derivatives of 1,2,2-trimethylcyclopentane. \u003cem\u003eJournal of Fluorine Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0022-1139(97)00016-x\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0022-1139(97)00016-x\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMoloney et al. (1996). Chiral carboxylic acid ligands derived from camphoric acid. \u003cem\u003eTetrahedron: Asymmetry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/0957-4166(96)00328-x\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/0957-4166(96)00328-x\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085965865178,"sku":"TCI2510C001213922","price":1162000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085965897946,"sku":"TCI2510C001213923","price":3282000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0012_2364c1de-b9cd-4b80-8da7-a27c695a0c95.jpg?v=1792631978"},{"product_id":"tci2510c001313924","title":"TCI C0013 2792-42-9 (1R)-Camphor Oxime","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(1R)-Camphor Oxime from TCI is the oxime derivative of (1R)-camphor, a naturally occurring bicyclic compound that has long been valued as an inexpensive and readily available source of chirality. The oxime group forms when the carbonyl group of camphor reacts with hydroxylamine. This functional group opens many routes to further transformations while the rigid bornane skeleton stays intact. In synthetic laboratories, the compound serves as a chiral building block for optically active molecules, chiral ligands, and auxiliaries used in asymmetric synthesis.\u003c\/p\u003e\n\u003cp\u003eResearchers choose this material for two combined advantages: a defined absolute configuration and a rigid carbon framework. Because the bicyclic structure is rigid, the steric environment around the reaction centre is predictable, which makes the compound very useful for controlling stereoselectivity. The oxime group can be reduced to a primary amine, can undergo Beckmann rearrangement or fragmentation, or can act as a coordination site for metals. This versatility means a single starting material can give many different chiral derivatives without time-consuming resolution of racemates.\u003c\/p\u003e\n\u003cp\u003eIn Indonesia, this material is relevant to chemistry research groups at universities and research institutions working on asymmetric synthesis, natural product chemistry, and the development of chiral ligands and catalysts. Graduate students and synthetic chemists can use it as a dependable chiral starting point for multi-step synthesis projects and methodology studies. It also suits teaching laboratories that show how a natural chiral pool compound can be turned into useful stereodefined intermediates for modern organic synthesis.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSynthesis of chiral primary amines: the oxime group can be reduced to an amine on the rigid bornane skeleton, giving stereodefined amines for further derivatization and ligand construction.\u003c\/li\u003e\n\u003cli\u003ePreparation of chiral ligands for metal catalysis: the oxime can act as a metal coordination site, and the rigid camphor framework gives a predictable steric environment for asymmetric catalysis research.\u003c\/li\u003e\n\u003cli\u003eDevelopment of chiral auxiliaries: its defined absolute configuration and rigid bicyclic structure help researchers control stereoselectivity in reactions where predictable facial selectivity is essential.\u003c\/li\u003e\n\u003cli\u003eBeckmann rearrangement and fragmentation studies: the oxime group undergoes these transformations, so it is useful for accessing new chiral nitrogen-containing scaffolds and for studying reaction mechanisms in teaching and research laboratories.\u003c\/li\u003e\n\u003cli\u003eChiral pool synthesis of optically active molecules: as a derivative of naturally abundant camphor, it gives an economical entry point to many chiral derivatives without the need for racemate resolution.\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\u003eProduct code: C0013\u003c\/li\u003e\n\u003cli\u003eCAS number: 2792-42-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Building Blocks\u003c\/li\u003e\n\u003cli\u003ePack sizes: standard TCI pack sizes; please contact AMI Scientific for available options\u003c\/li\u003e\n\u003cli\u003eStorage note: keep in a tightly closed container in a cool, dry place; refer to the TCI label and Safety Data Sheet\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore (1R)-Camphor Oxime in its original, tightly closed container in a cool, dry, well-ventilated area, away from heat sources, direct sunlight, and strong oxidizing agents. Keep the container closed when not in use to protect the material from moisture and contamination. Handle the compound in a fume hood or a well-ventilated workspace and wear suitable personal protective equipment, including safety glasses, gloves, and a laboratory coat. Avoid creating dust or inhaling it, and avoid contact with skin and eyes. Always follow the TCI Safety Data Sheet for specific hazard information, storage requirements, and disposal instructions under your institution's chemical waste procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085965963482,"sku":"TCI2510C001313924","price":783000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085965996250,"sku":"TCI2510C001313925","price":2373000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085966029018,"sku":"TCI2510C001313926","price":7495000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0013.jpg?v=1771059006"},{"product_id":"tci2510c001413927","title":"TCI C0014 10373-78-1 (+\/-)-Camphorquinone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0014 (+\/-)-Camphorquinone, CAS 10373-78-1, is a bicyclic 1,2-diketone widely used as a visible-light photoinitiator. Combined with a tertiary amine co-initiator, it generates free radicals that initiate the curing of methacrylate-based resins and coatings. Because it absorbs in the visible region, curing can be controlled without UV irradiation, which is valuable in dental and photocurable materials research. AMI Scientific supplies this TCI product in 5 g and 25 g pack sizes, and it should be stored protected from light.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003e(2002). CAMPHORQUINONE AND CAMPHORQUINONE MONOXIME. \u003cem\u003eOrganic Syntheses\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.15227\/orgsyn.079.0125\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.15227\/orgsyn.079.0125\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSionkowska et al. (2002). The influence of camphorquinone on the photochemical stability of cellulose. \u003cem\u003ePolymer Degradation and Stability\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0141-3910(02)00131-3\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0141-3910(02)00131-3\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSionkowska et al. (1999). Comparison of the photopolymerization kinetics of triethyleneglycol dimethacrylate initiated by camphorquinone\/N-phenylglycine and camphorquinone\/D,L-α-phenylglycine. \u003cem\u003ePolymer Bulletin\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s002890050621\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s002890050621\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48085966061786,"sku":"TCI2510C001413927","price":1591000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085966094554,"sku":"TCI2510C001413928","price":4771000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0014_1a1c7f5e-8ed1-45de-abe8-d906665481b3.jpg?v=1792631982"},{"product_id":"tci2510c001513929","title":"TCI C0015 3144-16-9 (+)-10-Camphorsulfonic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0015 (+)-10-Camphorsulfonic Acid, CAS 3144-16-9, is a strong, optically active sulfonic acid built on the camphor framework. It is widely used as a resolving agent for racemic amines, forming diastereomeric salts that can be separated by crystallisation. The compound also serves as a convenient solid Brønsted acid catalyst for protection and deprotection steps, and as an ion-pairing additive in chromatography. AMI Scientific offers this TCI product in 25 g, 100 g, and 500 g pack sizes; because it is hygroscopic, keep the container tightly closed.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eZhang et al. (2002). Synthesis and characterization of self-assembled polyaniline nanotubes doped with D-10-camphorsulfonic acid. \u003cem\u003eNanotechnology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1088\/0957-4484\/13\/6\/311\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1088\/0957-4484\/13\/6\/311\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eYan et al. (1999). Thermoelectric Properties of Alternatively Layered Films of Polyaniline and (±)-10-Camphorsulfonic Acid-Doped Polyaniline. \u003cem\u003eChemistry Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1246\/cl.1999.1217\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1246\/cl.1999.1217\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eZhai et al. (2020). Anti-Corrosive Coating of Carbon-Steel Assisted by Polymer-Camphorsulfonic Acid Embedded within Graphene. \u003cem\u003eCoatings\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/coatings10090879\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/coatings10090879\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085966127322,"sku":"TCI2510C001513929","price":808000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085966160090,"sku":"TCI2510C001513930","price":1818000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085966192858,"sku":"TCI2510C001513931","price":4518000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0015_13748005-dc95-4e4d-ad8d-4b3e5b28eeed.jpg?v=1792631985"},{"product_id":"tci2510c001613932","title":"TCI C0016 5872-08-2 (+\/-)-10-Camphorsulfonic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(+\/-)-10-Camphorsulfonic Acid, commonly abbreviated as CSA, is an organic sulfonic acid derived from camphor and supplied in its racemic form. It is a strong acid, yet unlike many strong acids it is a solid and dissolves in a wide range of organic solvents. That combination makes it a practical acid catalyst for synthetic work. In glycoscience and carbohydrate chemistry, CSA is a well-known catalyst for acetal and ketal formation, including the installation of benzylidene and isopropylidene protecting groups on the hydroxyl groups of sugars.\u003c\/p\u003e\n\u003cp\u003eResearchers choose CSA because it pairs strong acidity with easy handling. Because it is a solid, it can be weighed more accurately than liquid mineral acids, which helps when catalyst loading has to be controlled closely. Its solubility in organic solvents lets it work as an effective homogeneous catalyst, so the reaction mixture stays uniform. Compared with some other sulfonic acids, CSA is often regarded as mild enough for sensitive substrates. It also forms salts with amines, so it is useful as a counterion, including as a dopant for polyaniline in conductive polymer research. Note that CSA is hygroscopic.\u003c\/p\u003e\n\u003cp\u003eIn Indonesia, CSA is useful to laboratories working in synthetic organic chemistry, carbohydrate chemistry, natural product chemistry, and materials science at universities and research institutions. Carbohydrate chemists use it for routine protecting group steps in multistep syntheses of sugar derivatives. Natural product groups use it as a convenient acid catalyst during the modification of isolated compounds. Materials science laboratories use it when preparing doped conductive polymers for electronic and sensing studies.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAcetal and ketal formation: CSA is a strong acid that dissolves in organic solvents, so it catalyzes acetal and ketal formation efficiently under homogeneous conditions.\u003c\/li\u003e\n\u003cli\u003eCarbohydrate protecting group chemistry: CSA is widely used to install benzylidene and isopropylidene protecting groups on sugar hydroxyl groups, which is a routine step in glycoscience synthesis.\u003c\/li\u003e\n\u003cli\u003eAcid catalysis for sensitive substrates: CSA is often considered milder than some other sulfonic acids, so it suits reactions where delicate functional groups must survive acidic conditions.\u003c\/li\u003e\n\u003cli\u003ePrecise catalyst dosing in synthesis: As a solid, CSA can be weighed more accurately than liquid mineral acids, which makes catalyst loading easier to control and reproduce between runs.\u003c\/li\u003e\n\u003cli\u003eConductive polymer research: CSA forms salts with amines and works as a counterion, which makes it useful as a dopant for polyaniline in conductive polymer studies.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI (product code C0016)\u003c\/li\u003e\n\u003cli\u003eCAS number: 5872-08-2\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Chemical Biology \u0026gt; Glycoscience\u003c\/li\u003e\n\u003cli\u003ePack sizes: refer to the available options on the product listing\u003c\/li\u003e\n\u003cli\u003ePhysical form: solid, racemic (+\/-) form\u003c\/li\u003e\n\u003cli\u003eStorage note: hygroscopic, so keep the container tightly closed and protect it from moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eStore (+\/-)-10-Camphorsulfonic Acid in its original tightly sealed container in a cool, dry, well-ventilated area. Because the material is hygroscopic, keep it away from humid air and close the container promptly after each use. A desiccator is a good choice for opened containers. Use chemically resistant containers suitable for strong acids, and keep the material away from bases and incompatible substances. CSA is a strong acid, so handle it with gloves, safety glasses, and a lab coat, and avoid creating or breathing dust. Weigh and transfer it in a fume hood or another well-ventilated area. Always follow the supplier's Safety Data Sheet and your institution's chemical safety procedures.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"25g","offer_id":48085966225626,"sku":"TCI2510C001613932","price":858000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085966258394,"sku":"TCI2510C001613933","price":2121000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085966291162,"sku":"TCI2510C001613934","price":5502000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0016_09924803-2e8a-415e-bee9-048d8e744abb.jpg?v=1792631988"}],"url":"https:\/\/amiscientific.com\/en\/collections\/chemicals-by-class-6-membered-carbocyclic-compounds.oembed?page=50","provider":"AMI Scientific","version":"1.0","type":"link"}