{"title":"Asymmetric Synthesis","description":"\u003cp\u003e\u003cstrong\u003eAsymmetric Synthesis\u003c\/strong\u003e — menghimpun auksiliari kiral, katalis dan ligan kiral, reagen resolusi kiral, serta building block kiral yang menjadi kunci sintesis enansioselektif. Kategori ini mencakup organokatalis prolin dan imidazolidinon MacMillan untuk reaksi katalisis asimetris organik.\u003c\/p\u003e\u003cp\u003eAsymmetric Synthesis dipakai kimiawan sintesis untuk reaksi reduksi, epoksidasi, hidroksilasi, dan borilasi enansioselektif menggunakan katalis logam kiral seperti kompleks salen-mangan atau ligan BINAP tersubstitusi. Auksiliari oksazolidinon dan organokatalis berbasis prolin digunakan pada reaksi transfer fase dan pembentukan ikatan karbon-karbon stereoselektif untuk sintesis molekul target dengan kemurnian enansiomer tinggi.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510i076136018\"\u003eTCI I0761 191090-32-1 (4R)-(+)-4-Isopropyl-5,5-diphenyl-2-oxazolidinone\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b551812165\"\u003eTCI B5518 105024-93-9 (R)-N-(2-Benzoylphenyl)-1-benzylpyrrolidine-2-carboxamide\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510i076236020\"\u003eTCI I0762 184346-45-0 (4S)-(-)-4-Isopropyl-5,5-diphenyl-2-oxazolidinone\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b551912167\"\u003eTCI B5519 96293-17-3 (S)-N-(2-Benzoylphenyl)-1-benzylpyrrolidine-2-carboxamide\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510a0546771\"\u003eTCI A0546 56-84-8 L-Aspartic Acid\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b553812198\"\u003eTCI B5538 1013028-26-6 3-tert-Butyl 4-Methyl (4R,5S)-2,2,5-Trimethyloxazolidine-3,4-dicarboxylate\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510x007156767\"\u003eTCI X0071 135139-00-3 (S)-(-)-XylBINAP\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b561312299\"\u003eTCI B5613 138124-32-0 (R,R)-(-)-N,N'-Bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminomanganese(III) Chloride\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan konfigurasi enansiomer (R atau S), kemurnian enansiomer (ee), serta kompatibilitas ligan kiral dengan logam pusat dan sistem pelarut reaksi yang digunakan. 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 Chemistry, sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/building-blocks-sintesis-organik\"\u003eBuilding Blocks untuk Sintesis Organik\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l2-chemical-biology\"\u003eChemical Biology\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l2-pharmaceutical-development-and-drug-discovery-research-reagents\"\u003ePharmaceutical Development and Drug Discovery Research Reagents\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/reagen-sintesis-organik\"\u003eReagen Sintesis Organik\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/katalis-dan-kimia-anorganik\"\u003eKatalis \u0026amp; Kimia Anorganik\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l2-catalysis-and-inorganic-chemistry\"\u003eCatalysis and Inorganic Chemistry\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKoleksi ini masih terbagi menjadi 12 kelompok yang lebih spesifik:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-chiral-building-blocks\"\u003eChiral Building Blocks\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-chiral-catalysts-chiral-ligands-chiral-reagents\"\u003eChiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-chiral-resolution-reagents\"\u003eChiral Resolution Reagents\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-chiral-resolving-reagents\"\u003eChiral Resolving Reagents\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-chiral-auxiliaries\"\u003eChiral Auxiliaries\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-proline-based-organocatalysts-asymmetric-synthesis\"\u003eProline-Based Organocatalysts [Asymmetric Synthesis]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-epoxidation-asymmetric-synthesis\"\u003eEpoxidation [Asymmetric Synthesis]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-reduction-asymmetric-synthesis\"\u003eReduction [Asymmetric Synthesis]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-phase-transfer-reaction-asymmetric-synthesis\"\u003ePhase Transfer Reaction [Asymmetric Synthesis]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-hydroxylation-asymmetric-synthesis\"\u003eHydroxylation [Asymmetric Synthesis]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-macmillan-imidazolidinone-organocatalysts-asymmetric-synthesis\"\u003eMacMillan Imidazolidinone Organocatalysts [Asymmetric Synthesis]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-borylation-asymmetric-synthesis\"\u003eBorylation [Asymmetric Synthesis]\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l1-chemistry\"\u003eChemistry\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":"tci2510b551812165","title":"TCI B5518 105024-93-9 (R)-N-(2-Benzoylphenyl)-1-benzylpyrrolidine-2-carboxamide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(R)-N-(2-Benzoylphenyl)-1-benzylpyrrolidine-2-carboxamide is a chiral compound widely used in asymmetric synthesis to produce molecules with specific stereochemistry. This material plays a crucial role in organic chemistry laboratories by enabling the selective formation of optically active compounds. Its application is essential for researchers aiming to achieve high enantiomeric purity in their synthetic processes. As a chiral auxiliary, it acts as a temporary stereocenter that directs the reaction pathway, facilitating the synthesis of complex molecules with precise stereochemical control.\u003c\/p\u003e\n\u003cp\u003eThe compound is valued for its structural complexity and its ability to form stable interactions with various reagents. These properties make it a preferred choice for chemists working in asymmetric synthesis. Its stability under standard laboratory conditions ensures consistent performance and simplifies storage and handling. Additionally, its molecular structure allows it to act as a versatile tool in a range of synthetic strategies, making it a reliable component in both academic and industrial research settings.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, particularly in educational institutions and research centers focused on asymmetric synthesis. Its relevance is heightened in applications requiring precise control over molecular structure, such as pharmaceutical development and advanced chemical synthesis. Its availability through suppliers like AMI Scientific supports local scientific communities in advancing their research goals.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis is a key application where this compound serves as a chiral auxiliary to control stereochemistry in complex molecule formation.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research benefits from its ability to direct reaction pathways, enabling the synthesis of optically active compounds with high enantiomeric purity.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical development utilizes this material to create chiral drugs, as many active pharmaceutical ingredients require specific stereochemistry for efficacy.\u003c\/li\u003e\n\u003cli\u003eAcademic research in Indonesian universities employs it to teach and explore advanced synthetic techniques in asymmetric chemistry.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical synthesis relies on its stability and reactivity to produce specialized compounds with controlled stereochemical properties.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 105024-93-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Auxiliaries\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\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 maintain chemical integrity. Proper labeling of storage containers is essential for safety and traceability. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles. While no specific hazards are indicated, general laboratory safety protocols should be followed to ensure safe handling and use. Regular monitoring of storage conditions is advised to maintain the compound's stability and effectiveness in research applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085884895450,"sku":"TCI2510B551812165","price":2121000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085884928218,"sku":"TCI2510B551812166","price":6940000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5518.jpg?v=1769144662"},{"product_id":"tci2510b551912167","title":"TCI B5519 96293-17-3 (S)-N-(2-Benzoylphenyl)-1-benzylpyrrolidine-2-carboxamide","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(S)-N-(2-Benzoylphenyl)-1-benzylpyrrolidine-2-carboxamide is a chiral compound widely used in asymmetric synthesis, playing a vital role in the development of chiral molecules. This compound is part of the chiral auxiliaries category, which are essential tools in organic chemistry for controlling stereochemistry during reactions. Its unique structure enables it to act as a chiral template, guiding the formation of specific enantiomers. In laboratory settings, it is particularly valuable for its ability to simplify complex synthetic pathways by reducing the number of steps required to achieve a desired product.\u003c\/p\u003e\n\u003cp\u003eOne of the key properties that make this compound a preferred choice is its high selectivity in binding to reactants, which enhances reaction efficiency and yields. Its molecular design allows for specific interactions with other reagents, making it ideal for applications where stereochemical control is critical. Additionally, its stability under various reaction conditions contributes to its reliability in synthetic processes. These characteristics make it a go-to compound for researchers aiming to produce compounds with defined stereochemistry and biological activity.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in pharmaceutical research and organic synthesis. It supports the development of new drugs and bioactive molecules by enabling precise control over stereochemistry. Researchers in academic and industrial settings rely on it for its effectiveness in creating chiral compounds with specific biological functions. Its application is particularly relevant in the fields of pharmacology and medicinal chemistry, where stereochemistry plays a crucial role in drug efficacy and safety.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric Synthesis: This compound is ideal for asymmetric synthesis due to its ability to direct the formation of specific enantiomers, enhancing the efficiency of complex reactions.\u003c\/li\u003e\n\u003cli\u003eChiral Auxiliary in Organic Chemistry: It functions as a chiral auxiliary, providing a template for stereocontrolled reactions, which is essential in the synthesis of bioactive compounds.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: It supports the development of new drugs by enabling the synthesis of chiral molecules with specific biological activities.\u003c\/li\u003e\n\u003cli\u003eMedicinal Chemistry Applications: Its use in medicinal chemistry allows for the creation of compounds with defined stereochemistry, crucial for drug development.\u003c\/li\u003e\n\u003cli\u003eAcademic and Industrial Research: It is widely used in both academic and industrial research settings to advance the field of organic synthesis and drug discovery.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 96293-17-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Auxiliaries\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various pack sizes as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid, typically in crystalline form\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 stability and effectiveness. 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 is important to handle it with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Avoid exposure to incompatible substances and ensure proper ventilation when handling. Regular monitoring of storage conditions is advised to maintain the integrity of the compound throughout its shelf life.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085884960986,"sku":"TCI2510B551912167","price":960000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085884993754,"sku":"TCI2510B551912168","price":3484000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5519_9ec259cf-16e5-4545-84de-7c9f806d41fa.jpg?v=1767862237"},{"product_id":"tci2510b553812198","title":"TCI B5538 1013028-26-6 3-tert-Butyl 4-Methyl (4R,5S)-2,2,5-Trimethyloxazolidine-3,4-dicarboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5538 3-tert-Butyl 4-Methyl (4R,5S)-2,2,5-Trimethyloxazolidine-3,4-dicarboxylate is a chiral building block designed for asymmetric synthesis applications. This oxazolidine derivative features defined (4R,5S) stereochemistry, making it a valuable intermediate for constructing enantiomerically pure compounds. It is commonly employed in medicinal chemistry research and drug development workflows that require precise stereochemical control.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085886107866,"sku":"TCI2510B553812198","price":2828000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5538.jpg?v=1767092486"},{"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":2979000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5613_9aff008e-8d59-44a2-b685-b6832842c906.jpg?v=1767862642"},{"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":50506878419162,"sku":"TCI2510B564712345","price":3207000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5647_09289751-b5e4-4b03-a0f1-c82cd2c355e8.jpg?v=1767862785"},{"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":2676000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085894136026,"sku":"TCI2510B564812348","price":9263000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5648_1444e967-cad8-493a-a142-cf8eb4fe863a.jpg?v=1767862792"},{"product_id":"tci2510b565712353","title":"TCI B5657 108149-65-1 tert-Butyl (S)-4-(Hydroxymethyl)-2,2-dimethyloxazolidine-3-carboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B5657 *tert*-Butyl (S)-4-(Hydroxymethyl)-2,2-dimethyloxazolidine-3-carboxylate (CAS 108149-65-1) is a high-purity chiral building block for asymmetric synthesis applications. This (S)-configured oxazolidine derivative serves as a versatile chiral auxiliary and protecting group in the stereoselective construction of complex organic molecules. It is particularly valuable in pharmaceutical research and academic laboratories for the synthesis of enantiomerically pure bioactive compounds, modified peptides, and chiral catalyst development.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085894332634,"sku":"TCI2510B565712353","price":3105000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085894365402,"sku":"TCI2510B565712354","price":10777000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5657_22d79aea-51d9-4815-adce-173c88eb6d08.jpg?v=1767862809"},{"product_id":"tci2510b570112414","title":"TCI B5701 848821-76-1 (S)-alpha,alpha-Bis[3,5-bis(trifluoromethyl)phenyl]-2-pyrrolidinemethanol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(S)-alpha,alpha-Bis[3,5-bis(trifluoromethyl)phenyl]-2-pyrrolidinemethanol is a chiral reagent widely used in asymmetric synthesis to produce compounds with specific stereochemical configurations. This compound plays a critical role in laboratory settings where precise control over molecular structure is essential. It is particularly valuable in research focused on creating enantiomerically pure substances, which are crucial in pharmaceutical and biochemical applications. Its unique molecular structure allows for selective interactions with substrates, enhancing the efficiency of complex chemical reactions.\u003c\/p\u003e\n\u003cp\u003eThe compound's chiral nature makes it a preferred choice for researchers aiming to achieve high enantioselectivity in synthetic processes. Its ability to act as a chiral catalyst or ligand enables the selective modification of molecules without interfering with the reaction pathway. This characteristic is vital for the development of bioactive compounds with specific pharmacological properties. Additionally, its stability under controlled conditions ensures consistent performance in various experimental setups, making it a reliable tool for both academic and industrial research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this reagent is commonly used in scientific research related to pharmacology, food chemistry, and materials science. It supports the development of new compounds with targeted biological activities, contributing to advancements in drug discovery and chemical innovation. Its application is widespread across research institutions and universities, where it is utilized to enhance the precision and effectiveness of synthetic processes in organic chemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis in pharmaceutical research due to its high enantioselectivity and ability to produce chiral compounds with specific stereochemistry.\u003c\/li\u003e\n\u003cli\u003eDevelopment of bioactive molecules in medicinal chemistry where precise molecular configuration is essential for biological activity.\u003c\/li\u003e\n\u003cli\u003eOrganic synthesis of complex molecules in academic research settings requiring controlled stereochemical outcomes.\u003c\/li\u003e\n\u003cli\u003eInvestigation of chiral catalytic systems in chemical engineering for industrial-scale production of enantiomerically pure products.\u003c\/li\u003e\n\u003cli\u003eExploration of new materials in polymer science where chiral structures influence material properties and functionality.\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: 848821-76-1\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory supply specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid or liquid, depending on formulation and supplier packaging\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 integrity. It is recommended to use airtight containers made of materials that are chemically inert to prevent degradation. Due to its chiral nature, it is important to handle the compound with care to avoid contamination or cross-contamination with other substances. Laboratory personnel should wear appropriate personal protective equipment, including gloves and safety goggles, when handling the material. Proper ventilation should be maintained in the workspace to ensure safe handling and minimize exposure risks. Regular monitoring of storage conditions is advised to ensure the compound remains effective for its intended applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085898068186,"sku":"TCI2510B570112414","price":3005000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5701.jpg?v=1767092687"},{"product_id":"tci2510b588212651","title":"TCI B5882 948595-00-4 (R)-Bis[3,5-bis(trifluoromethyl)phenyl](pyrrolidin-2-yl)methanol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(R)-Bis[3,5-bis(trifluoromethyl)phenyl](pyrrolidin-2-yl)methanol is a chiral reagent widely used in asymmetric synthesis to produce compounds with specific optical properties. This compound plays a crucial role in chemical reactions that require precise control over stereochemistry, making it an essential tool in modern laboratory settings. Its chiral nature allows it to selectively influence reaction pathways, leading to the formation of desired enantiomers with high efficiency. This compound is particularly valuable in pharmaceutical and organic chemistry research, where the stereochemistry of a molecule can significantly affect its biological activity.\u003c\/p\u003e\n\u003cp\u003eThe compound's unique structure, featuring trifluoromethyl groups, contributes to its distinct electronic and reactive properties. These groups enhance the molecule's ability to interact selectively with other chiral components in a reaction, improving the overall yield and reducing the formation of byproducts. Its high chiral purity and stability under controlled conditions make it a preferred choice for researchers aiming to achieve precise stereochemical outcomes. The compound’s effectiveness in asymmetric catalysis is further supported by its compatibility with a variety of reaction conditions and reagents.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used by chemists and pharmacologists working on the development of new compounds with specific biological activities. Its application in drug synthesis and organic chemistry research is widespread due to its ability to enhance reaction efficiency and provide precise stereochemical control. As a key component in chiral synthesis, it supports the advancement of pharmaceutical and chemical research in the region, offering a reliable and high-quality option for laboratory use.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric Synthesis: This compound is ideal for asymmetric synthesis due to its chiral structure, enabling the selective formation of enantiomers with high stereocontrol.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Research: It is widely used in drug development to create compounds with specific optical properties, enhancing their biological activity and efficacy.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Studies: Its unique electronic properties make it suitable for various organic reactions requiring precise stereochemical control.\u003c\/li\u003e\n\u003cli\u003eChiral Catalyst Development: It serves as a key reagent in the design and testing of new chiral catalysts for industrial and academic applications.\u003c\/li\u003e\n\u003cli\u003eBiologically Active Compound Synthesis: Its ability to influence reaction pathways makes it valuable in the synthesis of compounds with specific therapeutic applications.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 948595-00-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral 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 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 stability and effectiveness. It is recommended to use airtight containers made of materials that are chemically inert to prevent any unwanted reactions. Due to its chiral nature and potential reactivity, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. Proper ventilation should be maintained in the laboratory when working with this compound to ensure a safe working environment. All handling should be conducted in a controlled setting to minimize exposure and ensure compliance with standard laboratory safety protocols.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085908160730,"sku":"TCI2510B588212651","price":2399000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085908193498,"sku":"TCI2510B588212652","price":7295000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5882_2471edf7-857a-4fb7-a9a8-57bcdf9634fd.jpg?v=1767863728"},{"product_id":"tci2510b598512764","title":"TCI B5985 129648-07-3 1,2-Bis[(2R,5R)-2,5-dimethylphospholano]ethane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e1,2-Bis[(2R,5R)-2,5-dimethylphospholano]ethane is a chiral bidentate bisphospholane ligand widely used in asymmetric hydrogenation reactions with transition metal catalysts. It forms highly effective chiral complexes with rhodium and ruthenium, enabling the enantioselective reduction of prochiral olefins, ketones, and imines. This ligand is a reliable choice for pharmaceutical and fine chemical synthesis requiring high optical purity.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48085913075930,"sku":"TCI2510B598512764","price":3282000.0,"currency_code":"IDR","in_stock":true},{"title":"500mg","offer_id":48085913108698,"sku":"TCI2510B598512765","price":10071000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B5985_d672f8f2-2f0f-4676-bb0f-e77c5ee81da5.jpg?v=1767864076"},{"product_id":"tci2510b614612969","title":"TCI B6146 2102316-91-4 (-)-4-tert-Butyl-2,6-bis[(4S,5S)-4,5-tetramethylene-1-(2,4,6-trimethylbenzenesulfonyl)imidazolin-2-yl]phenol (contains 5% Dichloromethane at maximum)","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(-)-4-tert-Butyl-2,6-bis[(4S,5S)-4,5-tetramethylene-1-(2,4,6-trimethylbenzenesulfonyl)imidazolin-2-yl]phenol is a chiral bis(imidazoline) ligand designed for asymmetric synthesis applications. This compound features two (4S,5S)-configured imidazoline moieties attached to a tert-butyl-substituted phenol core, providing a well-defined chiral environment suitable for enantioselective catalytic reactions. It is commonly employed in asymmetric C-C and C-N bond-forming reactions and serves as a valuable tool in the development of new enantioselective synthetic methodologies.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"50mg","offer_id":48085922021594,"sku":"TCI2510B614612969","price":7926000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6146.jpg?v=1767093225"},{"product_id":"tci2510b618313010","title":"TCI B6183 160232-08-6 tert-Butyl [(2S,3R)-3-Hydroxy-4-(isobutylamino)-1-phenylbutan-2-yl]carbamate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6183 tert-Butyl [(2S,3R)-3-Hydroxy-4-(isobutylamino)-1-phenylbutan-2-yl]carbamate is a high-purity chiral building block specifically designed for asymmetric synthesis research. This compound features a well-defined (2S,3R) stereochemistry, making it a valuable intermediate for constructing complex chiral molecules. Its primary applications include pharmaceutical development, particularly in the synthesis of protease inhibitors and peptidomimetics requiring strict enantiomeric control.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085923758298,"sku":"TCI2510B618313010","price":1868000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085923791066,"sku":"TCI2510B618313011","price":6511000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6183.jpg?v=1768816002"},{"product_id":"tci2510b624013072","title":"TCI B6240 1448897-87-7 (1R,2R)-1,2-Bis(4-methylphenyl)ethylenediamine Dihydrochloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(1,2)-1,2-Bis(4-methylphenyl)ethylenediamine Dihydrochloride is a chiral compound widely used in asymmetric synthesis to produce molecules with specific stereochemistry. This material functions as a chiral reagent or catalyst, enabling precise control over the stereochemical outcome of chemical reactions. In laboratory settings, it plays a crucial role in the development of chiral compounds, particularly those with biological activity, such as pharmaceuticals and industrial chemicals. Its ability to influence reaction pathways makes it an essential tool for researchers aiming to achieve high enantiomeric purity.\u003c\/p\u003e\n\u003cp\u003eThe compound’s molecular structure, featuring two methylphenyl groups, provides high selectivity towards specific substrates, enhancing reaction efficiency and yield. Its chemical stability ensures consistent performance across multiple experimental runs. Additionally, its availability in dihydrochloride form simplifies handling and storage, making it a practical choice for laboratory use. The compound’s versatility and effectiveness in controlling stereochemistry make it a preferred option for advanced synthetic chemistry applications.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in organic chemistry research, particularly in asymmetric synthesis and the development of new chemical materials. It is a key component in experiments requiring precise stereoselective control, supporting research in pharmaceutical development and industrial chemical synthesis. Its application is widespread among research institutions and universities, contributing to the advancement of chiral compound synthesis in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric Synthesis: This compound is ideal for creating chiral molecules with high enantiomeric purity, essential for pharmaceutical and industrial applications.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical Development: It supports the synthesis of bioactive compounds, aiding in drug discovery and formulation processes.\u003c\/li\u003e\n\u003cli\u003eOrganic Chemistry Research: Its role in controlling stereochemistry makes it a valuable tool for advanced synthetic pathways and structural modifications.\u003c\/li\u003e\n\u003cli\u003eIndustrial Chemical Synthesis: It enables the production of specialized chemicals with specific stereochemical properties, enhancing product performance.\u003c\/li\u003e\n\u003cli\u003eChiral Catalyst Studies: Its use in catalytic systems allows for the investigation of stereoselective reaction mechanisms and catalyst 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: 1448897-87-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per standard laboratory requirements\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid powder\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to use airtight containers to protect it from moisture and humidity, which could affect its performance. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Avoid exposure to high temperatures or direct sunlight, as these conditions may compromise its effectiveness. Proper storage and handling are essential to preserve its chiral properties and ensure consistent results in experimental applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48085926019290,"sku":"TCI2510B624013072","price":2071000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6240.jpg?v=1767093344"},{"product_id":"tci2510b634313200","title":"TCI B6343 51077-14-6 (S)-1-(tert-Butoxycarbonyl)azetidine-2-carboxylic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6343, also known as (S)-1-(tert-butoxycarbonyl)azetidine-2-carboxylic Acid, is a chiral building block essential in asymmetric synthesis. This compound is widely used in laboratories to create complex molecules with specific stereochemistry. Its azetidine ring structure, modified with a tert-butoxycarbonyl group, makes it a versatile tool for chemists aiming to control the spatial arrangement of atoms in organic molecules. This material plays a crucial role in the development of pharmaceuticals and bioactive compounds, where precise stereochemistry is required for biological activity.\u003c\/p\u003e\n\u003cp\u003eThe compound is favored for its chemical stability under controlled conditions and its solubility in various organic solvents. These properties make it an ideal candidate for use in a wide range of synthetic reactions. Its ability to act as a precursor in asymmetric reactions allows for the selective formation of stereoisomers, which is essential in drug development and fine chemical synthesis. The compound's reliability and reproducibility in laboratory settings make it a preferred choice for researchers working on complex molecular structures.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is commonly used in research related to pharmacology, organic chemistry, and biochemistry. It is particularly valuable in the development of new drugs and in the study of molecular mechanisms. Many research institutions and universities in Indonesia rely on this material to advance their scientific work and contribute to the field of medicinal chemistry.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis is a key application where this compound enables the selective formation of stereoisomers, crucial for drug development and bioactive compound creation.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research benefits from its role as a chiral building block, allowing for the synthesis of complex molecules with controlled stereochemistry.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical research utilizes this compound to develop new drugs, as its stereochemistry can influence biological activity and pharmacological properties.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies often incorporate this material to investigate molecular interactions and structural requirements for biological function.\u003c\/li\u003e\n\u003cli\u003eIt is also used in the synthesis of fine chemicals, where precise stereochemical control is essential for industrial and research applications.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 51077-14-6\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral 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 moisture and direct sunlight\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment to maintain its chemical stability. It is recommended to keep it in a sealed container to prevent exposure to moisture and air. Due to its organic nature, it is best stored in airtight glass or plastic containers that are resistant to chemical degradation. Proper labeling and storage conditions are essential to ensure the integrity of the material. In laboratory settings, it should be handled with care, using appropriate personal protective equipment. Regular monitoring of storage conditions is advised to maintain the quality and effectiveness of the compound for research purposes.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085931851994,"sku":"TCI2510B634313200","price":2626000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6343.jpg?v=1767093516"},{"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":3434000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085937619162,"sku":"TCI2604B639041","price":13325000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6390_733bda7c-e15c-4504-b30f-33f31b557564.jpg?v=1767865604"},{"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":3434000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085937750234,"sku":"TCI2510B639313273","price":13503000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6393_d3d375f2-12ec-42f0-9f22-168ec7a061e2.jpg?v=1767865612"},{"product_id":"tci2510b640013283","title":"TCI B6400 170033-47-3 tert-Butyl (R)-2-Methylpiperazine-1-carboxylate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6400, tert-butyl (R)-2-methylpiperazine-1-carboxylate (CAS 170033-47-3), is a mono-Boc-protected chiral piperazine building block with defined (R) configuration at C-2. The selective protection leaves the N-4 nitrogen free for alkylation, acylation, sulfonylation, reductive amination, or Buchwald–Hartwig coupling. Subsequent acid-mediated Boc removal unmasks the second nitrogen for further elaboration, making the reagent well suited to multi-step medicinal chemistry routes. AMI Scientific supplies it in 1 g and 5 g packs; refer to the lot Certificate of Analysis for stereochemical and purity data.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSTUDER et al. (1995). ChemInform Abstract: Synthesis and First Applications of a New Chiral Auxiliary (tert‐Butyl 2‐(tert‐Butyl)‐5,5‐dimethyl‐4‐oxoimidazolidine‐1‐carboxylate) (V).. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199547157\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199547157\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMamat et al. (2012). Synthesis and Molecular Structure of tert-Butyl 4-(2-tert-butoxy-2-oxoethyl)piperazine-1-carboxylate. \u003cem\u003eCrystals\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/cryst2010090\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/cryst2010090\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eGrauer et al. (2009). Synthesis of rac-tert-butyl 3-(benzyloxycarbonylamino)-2-(4-bromophenyl)-tetrahydrofuran-3-carboxylate. \u003cem\u003eMolbank\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/m596\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/m596\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":48085938208986,"sku":"TCI2510B640013283","price":1010000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085938241754,"sku":"TCI2510B640013284","price":3484000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6400_d10dda81-1f79-4d4e-b518-b61c3a510bbe.jpg?v=1767865644"},{"product_id":"tci2510b661113567","title":"TCI B6611 848821-61-4 (2S)-2-[Bis[3,5-bis(trifluoromethyl)phenyl][(trimethylsilyl)oxy]methyl]pyrrolidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6611, with the CAS number 848821-61-4, is a complex chiral compound that plays a vital role in asymmetric synthesis. This material is specifically designed for use in chemical laboratories where precise control over stereochemistry is essential. Its unique molecular structure allows it to act as a chiral reagent, facilitating the synthesis of enantiomerically pure compounds. In the context of modern organic chemistry, this compound is indispensable for achieving high enantioselectivity in various reactions.\u003c\/p\u003e\n\u003cp\u003eOne of the key attributes of TCI B6611 is its highly complex chiral architecture, which enables it to interact selectively with specific substrates. This property makes it an ideal choice for researchers aiming to develop efficient and targeted synthetic pathways. The compound’s stability under certain conditions further enhances its utility, allowing for consistent performance in laboratory settings. Its ability to direct chemical reactions with high specificity is a major factor in its popularity among chemists working in the field of asymmetric synthesis.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, TCI B6611 is widely used in organic chemistry research, particularly in the development of bioactive compounds and pharmaceuticals. It is a preferred tool for academic and industrial researchers who require precise control over stereochemical outcomes. Its application extends to various areas of chemical synthesis, making it a valuable asset in both academic and applied research environments.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis in organic chemistry laboratories for the production of enantiomerically pure compounds.\u003c\/li\u003e\n\u003cli\u003eDevelopment of bioactive molecules and pharmaceuticals requiring precise stereochemical control.\u003c\/li\u003e\n\u003cli\u003eResearch in chiral catalysis and ligand design for advanced synthetic methodologies.\u003c\/li\u003e\n\u003cli\u003eInvestigation of reaction mechanisms involving chiral reagents and substrates.\u003c\/li\u003e\n\u003cli\u003eSupport for academic and industrial research in drug discovery and chemical innovation.\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: 848821-61-4\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\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. Due to its complex molecular structure, it is important to handle it with care to avoid contamination or degradation. Laboratory personnel should ensure proper ventilation when working with this material. Always follow standard safety protocols for handling chiral compounds, including the use of personal protective equipment. The compound is not known to be hazardous under normal storage conditions, but it is advisable to follow general chemical safety guidelines to ensure safe handling and use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085950202074,"sku":"TCI2510B661113567","price":6790000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6611.jpg?v=1767094028"},{"product_id":"tci2510b679513709","title":"TCI B6795 114446-55-8 (S)-1-(2-Bromophenyl)ethan-1-ol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6795 (CAS 114446-55-8) is (S)-1-(2-bromophenyl)ethan-1-ol, a chiral benzylic alcohol bearing an ortho-bromo substituent. The pre-installed stereocentre makes it a practical starting point for asymmetric synthesis and chiral ligand preparation. Its ortho-bromine serves as a handle for palladium-catalysed cross-coupling and for intramolecular cyclisation toward oxygen heterocycles. AMI Scientific offers this TCI reagent in 1 g and 5 g pack sizes for research use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085956427994,"sku":"TCI2510B679513709","price":1363000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085956460762,"sku":"TCI2510B679513710","price":4721000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6795.jpg?v=1768816102"},{"product_id":"tci2510b683913744","title":"TCI B6839 100760-04-1 (S)-1-(4-Bromophenyl)ethan-1-ol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6839 (S)-1-(4-Bromophenyl)ethan-1-ol is a chiral secondary benzylic alcohol that combines a defined stereocentre with a synthetically versatile aryl bromide handle. It is widely used as a chiral building block and as a reference enantiomer when evaluating asymmetric ketone reductions, including ketoreductase-based biocatalysis. The bromine substituent allows straightforward elaboration through Suzuki, Sonogashira, or Buchwald–Hartwig cross-coupling chemistry. AMI Scientific supplies this TCI product in 1 g and 5 g research-scale packs suitable for method development and optimisation work.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085957705946,"sku":"TCI2510B683913744","price":1339000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085957738714,"sku":"TCI2510B683913745","price":4669000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6839.jpg?v=1769180278"},{"product_id":"tci2510b687813781","title":"TCI B6878 76155-78-7 (R)-1-(4-Bromophenyl)ethan-1-ol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI B6878 (CAS 76155-78-7) is (R)-1-(4-bromophenyl)ethan-1-ol, an enantiomerically defined benzylic alcohol carrying a para-bromo substituent. The secondary alcohol can be oxidised, esterified, converted to a leaving group or inverted under Mitsunobu conditions, while the aryl bromide remains available for palladium-catalysed cross-coupling. It also serves as a convenient reference material when developing chiral chromatographic methods or evaluating asymmetric ketone reduction. TCI offers 1 g and 5 g pack sizes; store cool, dry and protected from light, and refer to the Certificate of Analysis for chemical and enantiomeric purity data.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085959573722,"sku":"TCI2510B687813781","price":2221000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085959606490,"sku":"TCI2510B687813782","price":7698000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6878.jpg?v=1768816113"},{"product_id":"tci2510b692713811","title":"TCI B6927 131180-57-9 (S)-Bis(4-methoxyphenyl)(pyrrolidin-2-yl)methanol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(S)-Bis(4-methoxyphenyl)(pyrrolidin-2-yl)methanol is a chiral compound used in asymmetric synthesis to produce molecules with specific optical properties. This material plays a crucial role in laboratories where precise control over stereochemistry is required. It is commonly employed in reactions that demand chiral catalysts or ligands to enhance the efficiency and accuracy of chemical synthesis. Its unique molecular structure makes it a valuable reagent in the development of pharmaceuticals and complex organic compounds.\u003c\/p\u003e\n\u003cp\u003eThe compound's chiral nature allows for high selectivity in chemical reactions, minimizing the formation of by-products and improving the yield of the desired compound. Its molecular framework includes methoxy groups and a pyrrolidine ring, which contribute to its reactivity and specificity in various synthetic pathways. These features make it a preferred choice for researchers aiming to achieve controlled stereochemical outcomes. The compound's ability to influence reaction pathways with minimal side reactions is a key factor in its widespread use in advanced chemical research.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is widely utilized by chemists in educational institutions and research organizations. It is an essential component in the development of new pharmaceutical compounds and complex molecules. Its role in pharmacological and biochemical research underscores its importance in the scientific community. The compound is often used in studies that require precise optical control, making it a staple in modern chemical synthesis practices.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis is a key application where this compound is used to control the stereochemistry of products, offering high enantioselectivity in complex reactions.\u003c\/li\u003e\n\u003cli\u003ePharmaceutical development benefits from this compound's ability to selectively produce desired stereoisomers, which is crucial for drug efficacy and safety.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research relies on its chiral properties to facilitate the synthesis of complex molecules with specific optical configurations.\u003c\/li\u003e\n\u003cli\u003eBiochemical studies utilize this compound to explore enzyme-substrate interactions and molecular recognition processes in biological systems.\u003c\/li\u003e\n\u003cli\u003eAdvanced synthetic methodologies incorporate this compound to achieve controlled stereochemical outcomes in multi-step chemical processes.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 131180-57-9\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\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 keep it in a sealed container to prevent moisture absorption and contamination. Proper ventilation is essential when handling the material to minimize exposure to vapors. Due to its chiral nature, it is important to maintain strict purity standards to ensure consistent results in chemical reactions. Always use appropriate personal protective equipment, such as gloves and safety goggles, when working with this compound. Regular monitoring of storage conditions is advised to maintain its integrity and effectiveness in laboratory applications.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48085961212122,"sku":"TCI2510B692713811","price":8959000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510B6927.jpg?v=1767094392"},{"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":455000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085965734106,"sku":"TCI2510C001013919","price":2273000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0010.jpg?v=1767094541"},{"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.jpg?v=1769144599"},{"product_id":"tci2510c001313924","title":"TCI C0013 2792-42-9 (1R)-Camphor Oxime","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0013 (1R)-Camphor Oxime, CAS 2792-42-9, is a chiral oxime derived from the camphor skeleton with a defined (1R) configuration. The reactive C=N–OH group supports Beckmann rearrangements, reduction to chiral amines, and the construction of nitrogen heterocycles. Its rigid bicyclic framework and inherent chirality help direct stereochemical outcomes in asymmetric synthesis, while the oxime group can also coordinate metal centres as a chelating ligand. AMI Scientific supplies this TCI product in 1 g, 5 g, and 25 g pack sizes to match different experimental scales.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSchenone et al. (2001). ChemInform Abstract: O‐[2‐Hydroxy‐3‐(dialkylamino)propyl]ethers of (+)‐1,7,7‐Trimethyl Bicyclo[2.2.1]heptan‐2‐one Oxime (Camphor Oxime) with Analgesic and Antiarrhythmic Activities.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.200103157\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.200103157\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":48085965963482,"sku":"TCI2510C001313924","price":733000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48085965996250,"sku":"TCI2510C001313925","price":2323000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48085966029018,"sku":"TCI2510C001313926","price":7445000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0013.jpg?v=1771059006"},{"product_id":"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":758000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085966160090,"sku":"TCI2510C001513930","price":1768000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48085966192858,"sku":"TCI2510C001513931","price":4468000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0015.jpg?v=1767094558"},{"product_id":"tci2510c004713980","title":"TCI C0047 498-15-7 (+)-3-Carene","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(+)-3-Carene (TCI C0047, CAS 498-15-7) is a chiral bicyclic monoterpene found naturally in turpentine and conifer essential oils. Its fused cyclopropane carane skeleton and built-in stereocentres make it a practical chiral-pool starting material for asymmetric synthesis and chiral ligand preparation. It also serves as an analytical reference in essential oil profiling by gas chromatography. Available in 25 mL and 500 mL bottles, this flammable, volatile liquid should be handled in a fume hood and stored tightly closed in a cool, well-ventilated area away from ignition sources and oxidisers.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eDvorakova et al. (2011). Biotransformation of (1S)-2-Carene and (1S)-3-Carene by Picea abies Suspension Culture. \u003cem\u003eMolecules\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3390\/molecules161210541\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3390\/molecules161210541\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHidayati et al. (2016). Studi Perlakuan Reaksi Isomerisasi 3-Carene Menjadi 4-Carene Menggunakan Katalis Natrium-O-Klorotoluena. \u003cem\u003eChemical\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.20885\/chemical.vol2.iss1.art2\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.20885\/chemical.vol2.iss1.art2\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMacaev et al. (2006). Use of monoterpenes, 3-carene and 2-carene, as synthons in the stereoselective synthesis of 2,2-dimethyl-1,3-disubstituted cyclopropanes. \u003cem\u003eTetrahedron\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.tet.2005.09.001\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.tet.2005.09.001\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":"25mL","offer_id":48085968257242,"sku":"TCI2510C004713980","price":960000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48085968290010,"sku":"TCI2510C004713981","price":2424000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0047.jpg?v=1768816135"},{"product_id":"tci2510c034714413","title":"TCI C0347 485-71-2 Cinchonidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0347 Cinchonidine, CAS 485-71-2, is a cinchona alkaloid that has long served as a workhorse reagent in asymmetric synthesis. Its quinoline ring, basic quinuclidine nitrogen, and secondary hydroxyl group at a stereogenic centre allow it to act simultaneously as a chiral base and a hydrogen-bond donor. It is applied as an organocatalyst, as a chiral modifier for heterogeneous hydrogenation catalysts, as a resolving agent for racemic acids, and as a starting material for cinchona-derived phase transfer catalysts and ligands. AMI Scientific offers this TCI product in 25 g and 100 g packs, with lot-specific data available from the manufacturer.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003e(2018). Synthesis of (+)-Cinchonidine. \u003cem\u003eSynfacts\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/s-0037-1611233\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/s-0037-1611233\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eBeresford (2004). Enantioselective Addition of Diethylzinc to N‐Diphenylphosphinoylimines Employing Cinchonidine and Cinchonine as Chiral Ligands.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.200446025\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.200446025\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eLindholm et al. (2003). Hydrosilylation of Cinchonidine and 9‐O‐TMS‐Cinchonidine with Triethoxysilane: Application of 11‐(Triethoxysilyl)‐10,11‐dihydrocinchonidine as a Chiral Modifier in the Enantioselective Hydrogenation of 1‐Phenylpropane‐1,2‐dione.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.200318077\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.200318077\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":48085991456986,"sku":"TCI2510C034714413","price":2273000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48085991489754,"sku":"TCI2510C034714414","price":6790000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0347.jpg?v=1767095063"},{"product_id":"tci2510c035014417","title":"TCI C0350 118-10-5 Cinchonine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eCinchonine (TCI C0350, CAS 118-10-5) is a naturally occurring cinchona alkaloid and one of the most established chiral catalysts in asymmetric synthesis. Because it behaves as a pseudo-enantiomer of cinchonidine, the two are frequently paired to access opposite stereochemical outcomes within the same reaction system. It also serves as a starting scaffold for chiral phase-transfer catalysts and as a resolving agent for racemic acids. AMI Scientific offers this TCI product in 25 g and 200 g packs to suit both small-scale studies and more intensive synthetic work.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBartók et al. (2005). Enantioselective hydrogenation of ethyl pyruvate catalysed by cinchonine-modified Pt\/Al2O3: tilted adsorption geometry of cinchonine. \u003cem\u003eCatalysis Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s10562-004-3449-2\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s10562-004-3449-2\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHuaizhi et al. (2000). Study on Adsorption Properties of Cinchonine Loaded Resin to Mo and V by ICP-AES. \u003cem\u003eAnalytical Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1080\/00032710008543172\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1080\/00032710008543172\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eXi et al. (2013). Cinchonine and thiourea. \u003cem\u003eChemical Communications\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1039\/c3cc40825f\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1039\/c3cc40825f\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":48085991620826,"sku":"TCI2510C035014417","price":1465000.0,"currency_code":"IDR","in_stock":true},{"title":"200g","offer_id":48085991653594,"sku":"TCI2510C035014418","price":7850000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0350.jpg?v=1767095075"},{"product_id":"tci2510c070314952","title":"TCI C0703 6485-40-1 (R)-(-)-Carvone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0703 (R)-(-)-Carvone, CAS 6485-40-1, is the R-enantiomer of the chiral monoterpenoid ketone responsible for the characteristic spearmint aroma. Its enone framework and pre-installed stereocenter make it a widely used chiral-pool starting material for asymmetric synthesis and terpenoid total synthesis. AMI Scientific supplies this TCI reagent in 25 mL, 100 mL, and 500 mL packs for organic chemistry, natural product, and flavor research laboratories. Store the container tightly closed in a cool, dark place, and wear gloves and eye protection because carvone may cause skin irritation or sensitization.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNUNES et al. (2005). Gas-phase ozonolysis of the monoterpenoids ()-(+)-carvone, ()-(−)-carvone, (−)-carveol, geraniol and citral. \u003cem\u003eAtmospheric Environment\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.atmosenv.2005.04.009\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.atmosenv.2005.04.009\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSrikrishna et al. (2000). ChemInform Abstract: Chiral Synthons from Carvone. Part 40. A Simple, Enantiospecific Approach to Both Enantiomers of 1α,25‐Dihydroxyvitamin D3 A‐Ring Precursors from R‐Carvone.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.200036238\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.200036238\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eBenavente et al. (2017). Selective production of carvacrol from carvone over supported Pd catalysts. \u003cem\u003eCatalysis Communications\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.catcom.2017.03.026\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.catcom.2017.03.026\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":"25mL","offer_id":48086022226138,"sku":"TCI2510C070314952","price":531000.0,"currency_code":"IDR","in_stock":true},{"title":"100mL","offer_id":48086022258906,"sku":"TCI2510C070314953","price":1237000.0,"currency_code":"IDR","in_stock":true},{"title":"500mL","offer_id":48086022291674,"sku":"TCI2510C070314954","price":3207000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0703.jpg?v=1768816317"},{"product_id":"tci2510c070414955","title":"TCI C0704 2244-16-8 (S)-(+)-Carvone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0704 (S)-(+)-Carvone, CAS 2244-16-8, is the S-enantiomer of carvone and carries the characteristic caraway aroma, making it a classic teaching example of chirality and olfaction. Chemically, its α,β-unsaturated ketone and isopropenyl group provide multiple handles for conjugate addition, selective reduction, and ring construction. AMI Scientific offers this TCI chiral building block in a 25 mL pack for asymmetric synthesis, natural product chemistry, and analytical method validation. Keep the bottle tightly closed in a cool, dark place and use gloves and eye protection during handling.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSRIKRISHNA et al. (1996). ChemInform Abstract: Chiral Synthons from Carvone. Part 16. Enantioselective Synthesis of Both (+)‐ and (‐)‐Derivatives of Bicyclo(4.3.0)nonan‐8‐one and ‐3,8‐ diones from (R)‐Carvone.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199626231\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199626231\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSrikrishna et al. (1990). Chiral synthons from carvone. Part 4. Radical cyclization strategies to bridged systems. Synthesis of bicyclo[3.2.1]octan-3-ones from (S)-carvone. \u003cem\u003eThe Journal of Organic Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1021\/jo00303a023\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1021\/jo00303a023\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eShing et al. (2006). Total Synthesis of (‐)‐Samaderine Y from (S)‐(+)‐Carvone.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.200616178\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.200616178\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":"25mL","offer_id":48086022324442,"sku":"TCI2510C070414955","price":1187000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0704.jpg?v=1768816317"},{"product_id":"tci2510c079715066","title":"TCI C0797 2186-24-5 2-[(p-Tolyloxy)methyl]oxirane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0797 2-[(p-Tolyloxy)methyl]oxirane (CAS 2186-24-5) is an aromatic glycidyl ether offered by AMI Scientific in 200 mg and 1 g research quantities. The strained epoxide ring opens readily with amines, alcohols, and other nucleophiles, giving direct access to amino alcohol and ether alcohol motifs. It is commonly employed as a chiral building block in asymmetric synthesis and in the preparation of pharmaceutical intermediates. Refer to the official TCI documentation for lot-specific quality data and safe handling guidance.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eGhosh et al. (2020). 2-Chloro-7-methyl-3-((4-((p-tolyloxy)methyl)-1H-1,2,3-triazol-1-yl)methyl) quinoline: Crystal structure, hydrogen bonding and anti-bacterial activity. \u003cem\u003eJournal of Molecular Structure\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.molstruc.2020.128137\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.molstruc.2020.128137\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":"200mg","offer_id":48086029500634,"sku":"TCI2510C079715066","price":1995000.0,"currency_code":"IDR","in_stock":true},{"title":"1g","offer_id":48086029533402,"sku":"TCI2510C079715067","price":6840000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0797.jpg?v=1767095778"},{"product_id":"tci2510c097215327","title":"TCI C0972 35963-20-3 (-)-10-Camphorsulfonic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0972 (-)-10-Camphorsulfonic Acid (CAS 35963-20-3) is a crystalline chiral sulfonic acid available in 25 g, 100 g, and 500 g pack sizes. It is widely used as a resolving agent for racemic amines, forming diastereomeric salts that can be separated by crystallization. The compound also serves as a strong Brønsted acid catalyst for acetal formation, deprotection, and related transformations. Store it tightly sealed in a cool, dry place and wear gloves and eye protection when weighing, as the solid is corrosive.\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\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\u003cli\u003eSong et al. (2013). Improved thermoelectric performance of PEDOT:PSS film treated with camphorsulfonic acid. \u003cem\u003eJournal of Polymer Research\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s10965-013-0316-0\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s10965-013-0316-0\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":48086040969434,"sku":"TCI2510C097215327","price":1237000.0,"currency_code":"IDR","in_stock":true},{"title":"100g","offer_id":48086041002202,"sku":"TCI2510C097215328","price":3458000.0,"currency_code":"IDR","in_stock":true},{"title":"500g","offer_id":48086041034970,"sku":"TCI2510C097215329","price":10600000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0972.jpg?v=1767096117"},{"product_id":"tci2510c099815371","title":"TCI C0998 21286-54-4 (+)-10-Camphorsulfonyl Chloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C0998 (+)-10-Camphorsulfonyl Chloride (CAS 21286-54-4) is a classic chiral building block that pairs the rigid, optically active camphor skeleton with a highly reactive sulfonyl chloride group. It is widely used as a chiral derivatizing agent, converting amines and alcohols into separable diastereomers for enantiomeric purity determination by HPLC or NMR. The same scaffold also serves as an entry point to camphorsultam-type chiral auxiliaries that direct stereoselectivity in alkylation and cycloaddition chemistry. AMI Scientific offers 5 g and 25 g packs; because the reagent is strongly moisture sensitive, handle it in a fume hood and store it tightly sealed in a cool, dry place, preferably under inert gas.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eKO et al. (1998). ChemInform Abstract: A Convenient Preparation of (1S)‐(+)‐10‐Mercaptoisoborneol from (1S)‐(+)‐10‐Camphorsulfonyl Chloride with High Diastereoselectivity.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199837217\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199837217\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":48086042738906,"sku":"TCI2510C099815371","price":1036000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086042771674,"sku":"TCI2510C099815372","price":3660000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C0998.jpg?v=1767096162"},{"product_id":"tci2510c118815644","title":"TCI C1188 40560-29-0 (S)-(+)-1-Chloro-2-methylbutane","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1188 (S)-(+)-1-Chloro-2-methylbutane, CAS 40560-29-0, is an enantiomerically defined alkyl chloride widely used as a chiral building block in asymmetric synthesis. Its primary carbon–chlorine bond undergoes nucleophilic substitution readily while the adjacent stereocentre remains intact, allowing chemists to transfer an optically active 2-methylbutyl group into larger frameworks. Typical applications include carbon–carbon bond formation, preparation of organometallic reagents, and the modification of liquid-crystalline and functional materials. AMI Scientific supplies this reagent in 10 mL and 25 mL packs for research laboratories, and users should always consult the manufacturer's Safety Data Sheet before handling.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10mL","offer_id":48086055452890,"sku":"TCI2510C118815644","price":2676000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086055485658,"sku":"TCI2510C118815645","price":4544000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1188.jpg?v=1769180331"},{"product_id":"tci2510c125115731","title":"TCI C1251 464-48-2 (-)-Camphor","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1251 (-)-Camphor (CAS 464-48-2) is a classic bicyclic terpenoid ketone offered as a chiral building block for asymmetric synthesis. Its rigid bornane framework provides a well-defined steric environment that reliably directs stereochemical outcomes in enolate alkylations, aldol reactions, and cycloadditions. It also serves as the starting point for widely used chiral auxiliaries such as camphorsulfonic acid and camphorsultam derivatives. Supplied by AMI Scientific in a 5 g pack, the material should be kept tightly closed because it sublimes readily at ambient conditions.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eProcter et al. (1999). ChemInform Abstract: Stereocontrolled Synthesis of Novel Enantiomerically Pure Sulfides and Selenides from (+)‐Camphor and (+)‐Camphor‐10‐sulfonyl Chloride.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199948097\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199948097\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e(2024). Camphor. \u003cem\u003eReactions Weekly\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s40278-024-53512-6\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s40278-024-53512-6\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e(2015). Camphor. \u003cem\u003eReactions Weekly\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s40278-015-3983-2\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s40278-015-3983-2\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":48086059122906,"sku":"TCI2510C125115731","price":2500000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1251.jpg?v=1768816467"},{"product_id":"tci2510c130815800","title":"TCI C1308 39262-22-1 (-)-10-Camphorsulfonyl Chloride","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1308 (-)-10-Camphorsulfonyl Chloride is a chiral sulfonyl chloride built on the rigid, optically active camphor skeleton. Its highly reactive sulfonyl chloride group readily couples with amines and alcohols to give sulfonamides and sulfonate esters under mild conditions. Researchers commonly use it to prepare camphor-derived chiral auxiliaries and ligands, and as a derivatizing reagent for enantiomeric analysis. Supplied by AMI Scientific in 5 g and 25 g packs, it should be kept dry and tightly closed because of its sensitivity to moisture.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eKO et al. (1998). ChemInform Abstract: A Convenient Preparation of (1S)‐(+)‐10‐Mercaptoisoborneol from (1S)‐(+)‐10‐Camphorsulfonyl Chloride with High Diastereoselectivity.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199837217\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199837217\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":48086062301402,"sku":"TCI2510C130815800","price":1742000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086062334170,"sku":"TCI2510C130815801","price":5603000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1308.jpg?v=1769144492"},{"product_id":"tci2510c132515820","title":"TCI C1325 94594-90-8 (-)-10,2-Camphorsultam","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1325 (-)-10,2-Camphorsultam, widely known as Oppolzer's sultam, is a classic chiral auxiliary built on the rigid camphor framework. Substrates are attached to the sultam nitrogen, transformed with high facial selectivity, and then released once the new stereocentre is set. It performs reliably in enolate alkylation, aldol reactions, Diels-Alder cycloadditions, and conjugate additions, and its crystalline derivatives often allow diastereomer purification. AMI Scientific supplies this TCI product in 1 g and 5 g packs, best stored cool, dry, and tightly closed.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBaciocchi et al. (1994). Stereoselective Heteroaromatic Homolytic Substitution with Carbon Radicals Derived from Oppolzer's Camphorsultam. \u003cem\u003eSynlett\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1055\/s-1994-23016\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1055\/s-1994-23016\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e(1990). (\u0026amp;#8722;)-D-2,10-CAMPHORSULTAM. \u003cem\u003eOrganic Syntheses\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.15227\/orgsyn.069.0154\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.15227\/orgsyn.069.0154\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eZhang et al. (2019). Asymmetric Difluoromethylthiolation of Carbon Nucleophiles with Optically Pure Difluoromethylthiolating Reagents Derived from Camphorsultam. \u003cem\u003eChinese Journal of Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/cjoc.201900298\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/cjoc.201900298\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":48086063186138,"sku":"TCI2510C132515820","price":455000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086063218906,"sku":"TCI2510C132515821","price":986000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1325.jpg?v=1769180338"},{"product_id":"tci2510c132615822","title":"TCI C1326 104322-63-6 (2R,8aS)-(+)-(Camphorylsulfonyl)oxaziridine [Asymmetric Oxidizing Reagent]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1326 (2R,8aS)-(+)-(Camphorylsulfonyl)oxaziridine is a chiral oxidizing reagent widely used in asymmetric synthesis laboratories. Its rigid camphorsulfonyl framework directs oxygen transfer toward one face of the substrate, enabling enantioselective transformations such as the hydroxylation of enolates to α-hydroxy carbonyl compounds and the oxidation of sulfides to chiral sulfoxides. Because the reaction proceeds through neutral oxygen transfer without transition metals, it suits substrates that are sensitive to strong acids or residual metal contamination. AMI Scientific supplies this reagent in research-scale packaging for academic, pharmaceutical, and industrial research laboratories in Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":50506853843162,"sku":"TCI2510C132615822","price":1439000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1326.jpg?v=1767096757"},{"product_id":"tci2510c132715824","title":"TCI C1327 104372-31-8 (2S,8aR)-(-)-(Camphorylsulfonyl)oxaziridine [Asymmetric Oxidizing Reagent]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1327 (2S,8aR)-(-)-(Camphorylsulfonyl)oxaziridine is the enantiomeric counterpart of the widely used camphor-derived chiral oxidant. Its rigid sulfonyl-camphor scaffold delivers oxygen preferentially to one face of the substrate, supporting enantioselective enolate hydroxylation and the preparation of chiral sulfoxides from sulfides. The metal-free oxygen transfer mechanism is valuable when the final product must remain free of transition-metal residues. AMI Scientific offers this reagent in research-scale packaging for organic chemistry, pharmaceutical, and academic laboratories across Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086063349978,"sku":"TCI2510C132715824","price":2045000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086063382746,"sku":"TCI2510C132715825","price":6537000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1327.jpg?v=1767096761"},{"product_id":"tci2510c136315883","title":"TCI C1363 88056-92-2 (-)-2-Cyano-6-phenyloxazolopiperidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1363 (-)-2-Cyano-6-phenyloxazolopiperidine (CAS 88056-92-2) is a bicyclic chiral synthon designed for the asymmetric synthesis of piperidine alkaloids. Its alpha-aminonitrile function is remarkably versatile: deprotonation generates a stabilised carbanion for reaction with electrophiles, while loss of cyanide delivers an iminium ion that reacts with nucleophiles. The chiral oxazolidine framework controls the facial approach of incoming reagents, giving substituted piperidines with high diastereoselectivity before the auxiliary is removed. AMI Scientific supplies this TCI chiral building block in a 1 g pack size for asymmetric synthesis research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086065807578,"sku":"TCI2510C136315883","price":5781000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1363.jpg?v=1767096849"},{"product_id":"tci2510c136515884","title":"TCI C1365 26782-74-1 (S)-2-Chloro-3-methylbutyric Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1365 (S)-2-Chloro-3-methylbutyric Acid (CAS 26782-74-1) is an enantiomerically defined chiral building block bearing an alpha-chloro substituent next to a branched isopropyl group. The alpha-chlorine acts as an excellent leaving group in bimolecular nucleophilic substitution, proceeding with predictable inversion of configuration and giving access to unnatural amino acids and chiral alpha-hydroxy acids. The free carboxylic acid remains available for esterification, amidation, or reduction, allowing sequential elaboration of both functional groups. AMI Scientific offers this TCI chiral building block in 1 g and 5 g pack sizes for asymmetric synthesis research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086065840346,"sku":"TCI2510C136515884","price":2550000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086065873114,"sku":"TCI2510C136515885","price":8355000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1365.jpg?v=1768816498"},{"product_id":"tci2510c137315895","title":"TCI C1373 29617-66-1 (S)-(-)-2-Chloropropionic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1373 (S)-(-)-2-Chloropropionic Acid (CAS 29617-66-1) is a compact and widely used chiral building block for asymmetric synthesis. Its secondary chloride is readily displaced by nucleophiles, often with inversion of configuration, giving chemists direct stereochemical control over the product. It is frequently employed to build aryloxypropionate frameworks, chiral auxiliaries, and other stereodefined intermediates. AMI Scientific stocks this TCI item in 1 g, 5 g, and 25 g pack sizes.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eWiddowson et al. (1996). Changes in Cerebellar Amino Acid Neurotransmitter Concentrations and Receptors Following Administration of the NeurotoxinL-2-Chloropropionic Acid. \u003cem\u003eToxicology and Applied Pharmacology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1006\/taap.1996.0006\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1006\/taap.1996.0006\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eEDBEİB (2020). 3-Chloropropionic Acid (3cp) Degradation and Production of Propionic Acid by Newly Isolated Fungus Trichoderma Sp. Mf1. \u003cem\u003eInternational Journal of Life Sciences and Biotechnology\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.38001\/ijlsb.677005\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.38001\/ijlsb.677005\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eLi et al. (2010). Manganese(III) acetate-mediated radical reaction of [60]fullerene with bromoacetic acid, 3-chloropropionic acid or 1-naphthylacetic acid. \u003cem\u003eChinese Science Bulletin\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s11434-010-4016-4\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s11434-010-4016-4\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":48086066299098,"sku":"TCI2510C137315895","price":1415000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086066331866,"sku":"TCI2510C137315896","price":4518000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086066364634,"sku":"TCI2510C137315897","price":14461000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1373.jpg?v=1769144484"},{"product_id":"tci2510c139115919","title":"TCI C1391 107869-45-4 (+)-10-Camphorsulfonimine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1391 (+)-10-Camphorsulfonimine (CAS 107869-45-4) is a chiral building block derived from the rigid camphor framework and used in asymmetric synthesis. Its sulfonimine group is most commonly oxidised to the corresponding camphor-derived oxaziridine, a well-established reagent for enantioselective oxygen transfer. Typical applications include asymmetric hydroxylation of enolates and the preparation of chiral sulfoxides from sulfides. AMI Scientific supplies the (+)-enantiomer in a 5 g pack, complementing the (-)-form for researchers who need access to both product configurations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086067216602,"sku":"TCI2510C139115919","price":2500000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1391.jpg?v=1769180345"},{"product_id":"tci2510c139315920","title":"TCI C1393 60886-80-8 (-)-10-Camphorsulfonimine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1393 (-)-10-Camphorsulfonimine (CAS 60886-80-8) is the opposite enantiomer of the camphor-derived sulfonimine used in asymmetric synthesis. Oxidation of its imine group affords a camphor-based oxaziridine that transfers oxygen with defined stereochemical preference. It is applied in enantioselective α-hydroxylation of carbonyl compounds and in the asymmetric oxidation of sulfides to chiral sulfoxides. Available from AMI Scientific in a 5 g pack, it lets researchers select the product configuration required by their synthetic route.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086067282138,"sku":"TCI2510C139315920","price":2247000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1393.jpg?v=1769144480"},{"product_id":"tci2510c144716005","title":"TCI C1447 20439-47-8 (1R,2R)-(-)-1,2-Cyclohexanediamine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1447 (1R,2R)-(-)-1,2-Cyclohexanediamine (CAS 20439-47-8) is an enantiopure trans vicinal diamine and a cornerstone chiral building block in asymmetric synthesis. Its two adjacent primary amines form a rigid bidentate donor set, ideal for salen ligands, Schiff bases, and transition metal complexes. It is equally valuable as the backbone of thiourea and squaramide organocatalysts. AMI Scientific supplies this TCI product in 5 g and 25 g packs; because the free diamine is basic and air-sensitive, handle it under the manufacturer's recommended conditions.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eHe et al. (2014). Synthesis, Characterization and Antitumor Activities of Cis-Chlorogenic Acid[(1R,2R)-1,2-Cyclohexanediamine] Platinum(II). \u003cem\u003eAdvanced Materials Research\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.4028\/www.scientific.net\/amr.884-885.593\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.4028\/www.scientific.net\/amr.884-885.593\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eHATA et al. (1992). Synthesis, Structure and Antitumor Activity of a Water-Soluble Platinum Complex, (1R,3R,4R,5R)-(-)-Quinato(1R,2R-cyclohexanediamine)platinum(II).. \u003cem\u003eChemical and Pharmaceutical Bulletin\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1248\/cpb.40.1604\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1248\/cpb.40.1604\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eYOON et al. (1998). ChemInform Abstract: (1R,2R)‐(‐)‐N,N′‐Bis (3,5‐di‐tert‐butylsalicylidene)‐1,2‐cyclohexanediamine: A Salen Ligand of Jacobsen′s Catalyst.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199812027\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199812027\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":48086070427866,"sku":"TCI2510C144716005","price":3508000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086070460634,"sku":"TCI2510C144716006","price":12972000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1447.jpg?v=1767096960"},{"product_id":"tci2510c144816007","title":"TCI C1448 21436-03-3 (1S,2S)-(+)-1,2-Cyclohexanediamine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1448 (1S,2S)-(+)-1,2-Cyclohexanediamine (CAS 21436-03-3) is the enantiomeric counterpart of the widely used trans-1,2-diaminocyclohexane scaffold. It allows researchers to reverse the sense of chiral induction while keeping the same catalytic system, giving access to either product enantiomer. Typical uses include salen and Schiff base ligand synthesis, transition metal complexation, and hydrogen-bonding organocatalysts. AMI Scientific offers this TCI product in 5 g and 25 g packs, to be handled under the manufacturer's recommended inert and dry conditions.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eGarbutcheon-Singh et al. (2016). Synthesis, characterisation and cytotoxicity of [(1,10-phenanthroline)(1R,2R,4R\/1S,2S,4S)-4-methyl-1,2-cyclohexanediamine)platinum(II)]2+ (PHEN-4-MeDACH). \u003cem\u003eInorganica Chimica Acta\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.ica.2015.10.048\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.ica.2015.10.048\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eZhang et al. (2010). Fixed helical Cd(II) coordination polymers assembled from diastereopure Schiff-base ligands derived from condensation of acetylacetone with 1S,2S- and 1R,2R-cyclohexanediamine. \u003cem\u003eInorganic Chemistry Communications\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.inoche.2010.05.015\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.inoche.2010.05.015\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eKaizaki et al. (1998). First solid state synthesis of the racemic compound and enantiomer of dinuclear Λ,Λ-di-μ-hydroxo-bis [bis((1S,2S)-1,2-transcyclohexanediamine)chromium(III)] and Δ,Δ-di-μ-hydroxo-bis [bis((1R, 2R)-1,2-trans-cyclohexanediamine) chromium (III)] bromides. \u003cem\u003eInorganica Chimica Acta\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0020-1693(97)06093-3\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0020-1693(97)06093-3\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":"5g","offer_id":48086070493402,"sku":"TCI2510C144816007","price":3837000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086070526170,"sku":"TCI2510C144816008","price":13351000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1448.jpg?v=1767096964"},{"product_id":"tci2510c144916009","title":"TCI C1449 39961-95-0 (1R,2R)-(+)-1,2-Cyclohexanediamine L-Tartrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1449 (1R,2R)-(+)-1,2-Cyclohexanediamine L-Tartrate (CAS 39961-95-0) is the tartrate salt form of a key chiral diamine used in asymmetric synthesis. As a stable solid, it is easier to weigh and store than the free base and is protected from atmospheric carbon dioxide and moisture. The free diamine is typically liberated with base before use in salen ligands, Schiff bases, or hydrogen-bonding organocatalysts. AMI Scientific supplies this TCI product in 5 g and 25 g packs for asymmetric catalysis and coordination chemistry laboratories.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086070591706,"sku":"TCI2510C144916009","price":834000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086070624474,"sku":"TCI2510C144916010","price":2726000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1449.jpg?v=1769144473"},{"product_id":"tci2510c145016011","title":"TCI C1450 67333-70-4 (1S,2S)-(-)-1,2-Cyclohexanediamine D-Tartrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1450 (1S,2S)-(-)-1,2-Cyclohexanediamine D-Tartrate (CAS 67333-70-4) is the stable tartrate salt of the (1S,2S) trans-diaminocyclohexane scaffold. The salt form simplifies weighing and long-term storage while protecting the amine groups from air and moisture. After liberation with base, the diamine serves in salen ligands, Schiff bases, and thiourea or squaramide organocatalysts with the opposite sense of chiral induction. AMI Scientific offers this TCI product in 5 g and 25 g packs for asymmetric synthesis research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086070657242,"sku":"TCI2510C145016011","price":1162000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086070690010,"sku":"TCI2510C145016012","price":3686000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1450.jpg?v=1769180348"},{"product_id":"tci2510c145416018","title":"TCI C1454 5949-05-3 (-)-Citronellal","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1454 (-)-Citronellal (CAS 5949-05-3) is a chiral terpenoid aldehyde and a classic chiral pool starting material. Its aldehyde group, isolated alkene, and stereogenic centre make it ideal for stereocontrolled cyclisation chemistry, most notably the carbonyl-ene route to isopulegol. It is also widely used in terpenoid derivatisation, Lewis acid catalyst benchmarking, and flavour and fragrance research. AMI Scientific offers this TCI product in 5 mL and 25 mL packs; store it tightly closed and protected from light and air as directed by the manufacturer.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eJacob et al. (2009). ChemInform Abstract: Atom‐Economic Synthesis of Functionalized Octahydroacridines from Citronellal or 3‐(Phenylthio)‐citronellal.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.200951168\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.200951168\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eLu et al. (2014). Antioxidant Activity Determination of Citronellal and Crude Extracts of \u0026amp;lt;i\u0026amp;gt;Cymbopogon citratus\u0026amp;lt;\/i\u0026amp;gt; by 3 Different Methods. \u003cem\u003ePharmacology \u0026amp;amp; Pharmacy\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.4236\/pp.2014.54047\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.4236\/pp.2014.54047\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eJacob et al. (2009). Atom-Economic Synthesis of Functionalized Octahydroacridines from Citronellal or 3-(Phenylthio)-citronellal. \u003cem\u003eSynthetic Communications\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1080\/00397910802663469\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1080\/00397910802663469\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":"5mL","offer_id":48086070952154,"sku":"TCI2510C145416018","price":1062000.0,"currency_code":"IDR","in_stock":true},{"title":"25mL","offer_id":48086070984922,"sku":"TCI2510C145416019","price":3131000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1454.jpg?v=1768816527"}],"url":"https:\/\/amiscientific.com\/en\/collections\/tci-l2-asymmetric-synthesis.oembed?page=40","provider":"AMI Scientific","version":"1.0","type":"link"}