{"title":"Chiral Building Blocks","description":"\u003cp\u003e\u003cstrong\u003eChiral Building Blocks\u003c\/strong\u003e — menghimpun blok bangun kiral, baik heterosiklik maupun non-heterosiklik, bersama ligan istimewa dan kompleks logam untuk hidrogenasi asimetris. Kategori ini menyediakan fragmen enantiomurni yang menjadi titik awal sintesis senyawa dengan stereokimia terkendali.\u003c\/p\u003e\u003cp\u003eChiral Building Blocks dipakai kimiawan sintesis untuk merakit molekul target dengan pusat stereogenik tertentu, misalnya pada sintesis bahan aktif farmasi dan agrokimia melalui rute stereoselektif. Ligan dan kompleks logam dalam kategori ini juga berperan dalam reaksi hidrogenasi asimetris dan katalisis kiral lain untuk menghasilkan produk dengan kemurnian enantiomer tinggi.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510v007756498\"\u003eTCI V0077 4276-09-9 D-Valinol\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\/tci2510v007256492\"\u003eTCI V0072 1196-01-6 (-)-Verbenone\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b564712345\"\u003eTCI B5647 146504-07-6 (1R,2R)-N1-(tert-Butoxycarbonyl)-1,2-cyclohexanediamine\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510v005856471\"\u003eTCI V0058 2026-48-4 L-Valinol\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b564812347\"\u003eTCI B5648 180683-64-1 (1S,2S)-N1-(tert-Butoxycarbonyl)-1,2-cyclohexanediamine\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510t438556147\"\u003eTCI T4385 111769-26-7 (R)-Tetrahydrofuran-3-amine\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510b565712353\"\u003eTCI B5657 108149-65-1 tert-Butyl (S)-4-(Hydroxymethyl)-2,2-dimethyloxazolidine-3-carboxylate\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePerhatikan konfigurasi stereokimia (R\/S) dan kemurnian enantiomer (ee), karena kesalahan pemilihan isomer langsung memengaruhi hasil akhir sintesis asimetris. 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 Asymmetric Synthesis, sering dipakai bersamaan dalam satu alur kerja laboratorium:\u003c\/p\u003e\u003cul\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\u003c\/ul\u003e\u003cp\u003eKoleksi ini masih terbagi menjadi 4 kelompok yang lebih spesifik:\u003c\/p\u003e\u003cul\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-chiral-non-heterocyclic-building-blocks\"\u003eChiral Non-Heterocyclic Building Blocks\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-chiral-heterocyclic-building-blocks\"\u003eChiral Heterocyclic Building Blocks\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-privileged-ligands-and-complexes-asymmetric-synthesis\"\u003ePrivileged Ligands and Complexes [Asymmetric Synthesis]\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-hydrogenation-asymmetric-synthesis\"\u003eHydrogenation [Asymmetric Synthesis]\u003c\/a\u003e\u003c\/li\u003e\n\u003c\/ul\u003e\u003cp\u003eKembali ke \u003ca href=\"\/en\/collections\/tci-l2-asymmetric-synthesis\"\u003eAsymmetric Synthesis\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":"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":"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":"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":"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":"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":"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":"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":"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"},{"product_id":"tci2510c146616036","title":"TCI C1466 7540-51-4 (-)-beta-Citronellol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1466 (-)-beta-Citronellol is a chiral monoterpene alcohol with a characteristic rose-like floral aroma. It is widely used as a naturally derived chiral building block in asymmetric synthesis, where its primary hydroxyl group and alkene provide two convenient handles for further derivatisation. The compound also serves as a reference material in essential oil analysis and in fragrance and flavour research. AMI Scientific supplies it as a liquid in original TCI packaging, and containers should be kept tightly sealed away from heat and light to preserve quality.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eNaresh Yadav et al. (2018). Highly Efficient Stereoselective Glycosylation of \u0026amp;beta;-Citronellol. \u003cem\u003eAsian Journal of Organic \u0026amp; Medicinal Chemistry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.14233\/ajomc.2018.ajomc-p109\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.14233\/ajomc.2018.ajomc-p109\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eMaulina et al. (2025). In silico study of beta citronellol compound in lime plant (Citrus aurantifolia) as a drug candidate for enterovirus disease. \u003cem\u003eGreen and Tropical Laboratory for Sustainability\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.22219\/gtlabs.v2i1.41033\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.22219\/gtlabs.v2i1.41033\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":48086071705818,"sku":"TCI2510C146616036","price":1289000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1466.jpg?v=1768816533"},{"product_id":"tci2510c147416045","title":"TCI C1474 141942-85-0 Ethyl (R)-(-)-4-Cyano-3-hydroxybutyrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1474 Ethyl (R)-(-)-4-Cyano-3-hydroxybutyrate is an enantiomerically defined chiral building block bearing nitrile, hydroxyl, and ester functionalities. It is widely recognised as a key intermediate toward the chiral dihydroxy side chain found in statin-type pharmaceutical compounds. The nitrile can be reduced or hydrolysed, the ester further derivatised, and the chiral alcohol used directly to construct additional stereocentres. AMI Scientific supplies this reagent in original TCI packaging across three pack sizes, and it should be stored cool, dry, and tightly sealed following the manufacturer's label recommendations.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086072197338,"sku":"TCI2510C147416045","price":431000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086072230106,"sku":"TCI2510C147416046","price":657000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086072262874,"sku":"TCI2510C147416047","price":2221000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1474.jpg?v=1769144469"},{"product_id":"tci2510c148216057","title":"TCI C1482 10334-26-6 (1R)-(-)-Camphorquinone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1482 (1R)-(-)-Camphorquinone (CAS 10334-26-6) is an enantiomerically defined bicyclic α-diketone derived from the camphor skeleton. It is widely used as a visible-light photoinitiator for radical polymerisation, typically in combination with a tertiary amine co-initiator, and is well known in dental resin research. The rigid chiral framework also makes it a useful auxiliary and ligand precursor in asymmetric synthesis. Supplied in 1 g and 5 g packs; store protected from light and refer to the Safety Data Sheet.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eROY et al. (1998). ChemInform Abstract: An Efficient Synthesis of anti‐(1R)‐(+)‐Camphorquinone 3‐Oxime.. \u003cem\u003eChemInform\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/chin.199845099\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/chin.199845099\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eRoy (née Bhattacharaya) dkk. (1998). An efficient synthesis of anti-(1R)-(+)-camphorquinone 3-oxime. \u003cem\u003eTetrahedron Letters\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/s0040-4039(98)01307-0\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/s0040-4039(98)01307-0\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003e(2002). CAMPHORQUINONE AND CAMPHORQUINONE MONOXIME. \u003cem\u003eOrganic Syntheses\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.15227\/orgsyn.079.0125\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.15227\/orgsyn.079.0125\u003c\/a\u003e\n\u003c\/li\u003e\n\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":48086072623322,"sku":"TCI2510C148216057","price":1642000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086072656090,"sku":"TCI2510C148216058","price":3989000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1482.jpg?v=1768816541"},{"product_id":"tci2510c153116142","title":"TCI C1531 17430-98-7 (S)-(+)-1-Cyclohexylethylamine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI (S)-(+)-1-Cyclohexylethylamine (CAS 17430-98-7) is an enantiomerically defined chiral primary amine bearing a bulky cyclohexyl group. It is commonly used as a resolving agent for racemic carboxylic acids via diastereomeric salt formation, and as a removable chiral auxiliary in asymmetric synthesis. The compound also serves as a starting material for chiral ligands and as a derivatising reagent in enantiomeric purity analysis. AMI Scientific supplies 5 g and 25 g packs; keep tightly sealed away from air and moisture, and consult the manufacturer's Safety Data Sheet and Certificate of Analysis.\u003c\/p\u003e\n\u003cp\u003e---\u003c\/p\u003e\n\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSakai et al. (2006). Molecular mechanism of DCR phenomenon observed in (RS)-1-cyclohexylethylamine–mandelic acid resolution system. \u003cem\u003eTetrahedron: Asymmetry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.tetasy.2006.06.037\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.tetasy.2006.06.037\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003ePatel et al. (2012). Functionalization of Keggin type manganese substituted phosphotungstate by R-(−)-1-cyclohexylethylamine: Synthesis and characterization. \u003cem\u003eInorganica Chimica Acta\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.ica.2011.10.017\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.ica.2011.10.017\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eTurani‐I‐Belloto et al. (2023). Synthesis and Characterization of (R)‐N‐1‐Cyclohexylethylamine Borane. \u003cem\u003eChemistrySelect\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/slct.202301646\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/slct.202301646\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":48086076260570,"sku":"TCI2510C153116142","price":2247000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086076293338,"sku":"TCI2510C153116143","price":6537000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1531.jpg?v=1771058729"},{"product_id":"tci2510c154116152","title":"TCI C1541 5913-13-3 (R)-(-)-1-Cyclohexylethylamine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1541, (R)-(-)-1-Cyclohexylethylamine (CAS 5913-13-3), is a chiral amine widely applied in asymmetric synthesis and in the classical resolution of racemic carboxylic acids. The bulky cyclohexyl ring adjacent to the stereogenic centre creates an effective chiral environment for diastereomeric salt formation and selective crystallisation. It also serves as a chiral auxiliary, a precursor to chiral ligands, and a derivatising agent for enantiomeric purity determination. Supplied by AMI Scientific in a 5 g pack, this basic liquid should be handled in a fume hood and stored tightly closed in a cool, dry place.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eSakai et al. (2006). Molecular mechanism of DCR phenomenon observed in (RS)-1-cyclohexylethylamine–mandelic acid resolution system. \u003cem\u003eTetrahedron: Asymmetry\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.tetasy.2006.06.037\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.tetasy.2006.06.037\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003ePatel et al. (2012). Functionalization of Keggin type manganese substituted phosphotungstate by R-(−)-1-cyclohexylethylamine: Synthesis and characterization. \u003cem\u003eInorganica Chimica Acta\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1016\/j.ica.2011.10.017\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1016\/j.ica.2011.10.017\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eTurani‐I‐Belloto et al. (2023). Synthesis and Characterization of (R)‐N‐1‐Cyclohexylethylamine Borane. \u003cem\u003eChemistrySelect\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/slct.202301646\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/slct.202301646\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":48276383891674,"sku":"TCI2510C154116152","price":1995000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1541.jpg?v=1768816560"},{"product_id":"tci2510c154216154","title":"TCI C1542 60827-45-4 (S)-(+)-3-Chloro-1,2-propanediol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1542, (S)-(+)-3-Chloro-1,2-propanediol (CAS 60827-45-4), is a versatile chiral three-carbon synthon carrying two hydroxyl groups and one chloride. Base treatment converts it into an enantiomerically defined glycidol derivative, opening routes to chiral amino alcohols, modified glycerol frameworks, and chiral ligands. Its defined S configuration allows stereochemistry to be controlled from the very first step of a synthetic sequence. Available from AMI Scientific in 10 g and 25 g packs, it should be handled in a fume hood and stored tightly closed in a cool, dry place.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"10g","offer_id":48086076719322,"sku":"TCI2510C154216154","price":1491000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086076752090,"sku":"TCI2510C154216155","price":2576000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1542.jpg?v=1768816562"},{"product_id":"tci2510c160916254","title":"TCI C1609 58917-85-4 N-Carbobenzoxy-D-phenylalaninol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1609 N-Carbobenzoxy-D-phenylalaninol (CAS 58917-85-4) is a Cbz-protected chiral amino alcohol used as a defined stereochemical starting point in asymmetric synthesis. The free primary hydroxyl allows oxidation, activation, or substitution while the carbamate keeps the nitrogen protected until selective deprotection is required. Typical applications include chiral ligand and auxiliary preparation, peptidomimetic research, and comparative studies against the L-enantiomer. AMI Scientific supplies this TCI chiral building block in small research pack sizes, with all quality data referenced to the manufacturer's certificate of analysis.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086080913626,"sku":"TCI2510C160916254","price":733000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086080946394,"sku":"TCI2510C160916255","price":2500000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1609.jpg?v=1768204610"},{"product_id":"tci2510c161016256","title":"TCI C1610 6372-14-1 N-Carbobenzoxy-L-phenylalaninol","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1610 N-Carbobenzoxy-L-phenylalaninol (CAS 6372-14-1) is the L-configured Cbz-protected amino alcohol widely used as a chiral building block in asymmetric synthesis. Its combination of an aromatic ring, a stereogenic centre, a primary alcohol, and a protected amine offers multiple points for selective elaboration. Researchers apply it in peptidomimetic work, chiral ligand design, and the preparation of chiral heterocycles such as oxazolidines. AMI Scientific supplies this TCI product in a convenient 1 g research pack, and users should review the manufacturer's CoA and SDS before use.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086080979162,"sku":"TCI2510C161016256","price":481000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1610.jpg?v=1769144453"},{"product_id":"tci2510c163316283","title":"TCI C1633 77287-29-7 Methyl (R)-(+)-2-Chloropropionate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eMethyl (R)-(+)-2-Chloropropionate is a chiral compound widely used in asymmetric synthesis for the construction of optically active molecules. This compound plays a crucial role in organic chemistry research, particularly in the development of compounds with specific biological activities. Its chiral structure allows for the precise control of molecular configuration, making it an essential tool in asymmetric synthesis. The compound is commonly used in pharmaceutical and biotechnology research for the synthesis of complex molecules with targeted therapeutic applications. Its stability and availability in solid form make it a reliable choice for laboratory use. Due to its optical activity, it is ideal for applications requiring high specificity in chemical reactions, supporting the development of new compounds with potential medical uses.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086082027738,"sku":"TCI2510C163316283","price":3105000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1633.jpg?v=1767097247"},{"product_id":"tci2510c163416284","title":"TCI C1634 73246-45-4 Methyl (S)-(-)-2-Chloropropionate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eMethyl (S)-(-)-2-Chloropropionate (TCI C1634, CAS 73246-45-4) is a chiral building block widely used in asymmetric synthesis. Its specific stereochemistry makes it essential for creating molecules with precise spatial configurations, particularly in pharmaceutical and organic chemistry research. This compound is valued for its stability and reactivity in controlled chemical environments, enabling the synthesis of complex and bioactive compounds. Its application in Indonesian laboratories supports advancements in drug development and chemical innovation, making it a crucial component in modern scientific research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086082093274,"sku":"TCI2510C163416284","price":2524000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1634.jpg?v=1767097251"},{"product_id":"tci2510c165516313","title":"TCI C1655 7474-05-7 (R)-(+)-2-Chloropropionic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(R)-(+)-2-Chloropropionic acid is a chiral compound widely used in asymmetric synthesis for building complex molecular structures. Its chiral nature allows for the formation of different isomers, making it essential in reactions that require precise control over molecular configuration. This compound is commonly used in the synthesis of bioactive compounds, pharmaceuticals, and industrial chemicals. Its stability and reactivity make it a valuable tool in organic chemistry research. The compound is available in various packaging sizes, ensuring flexibility for different laboratory needs. It is recommended to store it in a sealed container away from light to maintain its integrity and effectiveness in experimental applications.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\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\u003cli\u003eHolmberg et al. (1992). Alcohol Induced Reversal of Enantioselectivity in a Lipase Catalyzed Resolution of 2-Chloropropionic Acid. \u003cem\u003eBiocatalysis\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.3109\/10242429209014875\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.3109\/10242429209014875\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":48086083141850,"sku":"TCI2510C165516313","price":1642000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086083174618,"sku":"TCI2510C165516314","price":4721000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086083207386,"sku":"TCI2510C165516315","price":16202000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1655.jpg?v=1768816594"},{"product_id":"tci2510c166016322","title":"TCI C1660 2767-84-2 (1S)-(+)-Camphorquinone","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e(1S)-(+)-Camphorquinone is a chiral compound widely used in asymmetric synthesis for the production of bioactive molecules. Its unique structure allows for the creation of compounds with specific stereochemistry, making it essential in pharmaceutical and biochemical research. This compound is particularly valuable in the development of new drugs due to its ability to form enantiomers with distinct biological activities. It is commonly used in laboratory settings for organic reactions and structural studies, especially in the field of medicinal chemistry. The compound is sensitive to oxidation and light, requiring careful handling and storage to maintain its integrity. Its role in creating complex molecular structures makes it a key component in advanced chemical research.\u003c\/p\u003e\n\u003ch3\u003eScientific References\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003e(2002). CAMPHORQUINONE AND CAMPHORQUINONE MONOXIME. \u003cem\u003eOrganic Syntheses\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.15227\/orgsyn.079.0125\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.15227\/orgsyn.079.0125\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eAllonas et al. (2001). Excited-State Properties of Camphorquinone Based Monomeric and Polymeric Photoinitiators. \u003cem\u003eHelvetica Chimica Acta\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1002\/1522-2675(20010919)84:9\u0026lt;2577::aid-hlca2577\u0026gt;3.0.co;2-q\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1002\/1522-2675(20010919)84:9\u0026lt;2577::aid-hlca2577\u0026gt;3.0.co;2-q\u003c\/a\u003e\n\u003c\/li\u003e\n\u003cli\u003eSionkowska et al. (1999). Comparison of the photopolymerization kinetics of triethyleneglycol dimethacrylate initiated by camphorquinone\/N-phenylglycine and camphorquinone\/D,L-α-phenylglycine. \u003cem\u003ePolymer Bulletin\u003c\/em\u003e \u003ca href=\"https:\/\/doi.org\/10.1007\/s002890050621\" target=\"_blank\" rel=\"nofollow noopener\"\u003edoi:10.1007\/s002890050621\u003c\/a\u003e\n\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003cp\u003e\u003csmall\u003eReferences were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.\u003c\/small\u003e\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086083469530,"sku":"TCI2510C166016322","price":1363000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086083502298,"sku":"TCI2510C166016323","price":3761000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1660.jpg?v=1769144447"},{"product_id":"tci2510c166316325","title":"TCI C1663 52950-18-2 2-Chloro-D-mandelic Acid","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003e2-Chloro-D-mandelic acid is a chiral compound widely used in asymmetric synthesis, particularly as a chiral building block in organic chemistry. Its unique molecular structure, featuring a chlorine group attached to a specific carbon atom, allows for the synthesis of complex molecules with specific stereochemistry. This compound is valuable in pharmaceutical research and chemical synthesis, where precise control over molecular structure is essential. It is commonly used in laboratory settings for developing new synthetic methods and studying biological activities of chiral compounds. Its versatility and specificity make it an important reagent in both academic and industrial research.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086083633370,"sku":"TCI2510C166316325","price":657000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086083666138,"sku":"TCI2510C166316326","price":2121000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1663.jpg?v=1768816674"},{"product_id":"tci2510c171716380","title":"TCI C1717 86728-85-0 Ethyl (S)-4-Chloro-3-hydroxybutyrate","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eEthyl (S)-4-Chloro-3-hydroxybutyrate is a chiral compound widely used in asymmetric synthesis for the construction of complex molecular structures. This compound plays a vital role in the development of pharmaceuticals and bioactive molecules due to its stereochemical properties. Its ability to participate in various synthetic reactions, such as SN2 and conjugate additions, makes it a valuable building block in organic chemistry. The compound is commonly used in research settings for the synthesis of new compounds with specific biological activities. Its chiral nature allows for precise control over the stereochemistry of the final product, which is crucial in drug development and advanced chemical research. This product is ideal for laboratories focusing on asymmetric synthesis and the creation of bioactive compounds.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"5g","offer_id":48086085664986,"sku":"TCI2510C171716380","price":1162000.0,"currency_code":"IDR","in_stock":true},{"title":"25g","offer_id":48086085697754,"sku":"TCI2510C171716381","price":3761000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1717.jpg?v=1768816688"}],"url":"https:\/\/amiscientific.com\/en\/collections\/tci-l3-chiral-building-blocks.oembed?page=26","provider":"AMI Scientific","version":"1.0","type":"link"}