{"title":"Hydroxylation [Asymmetric Synthesis]","description":"\u003cp\u003e\u003cstrong\u003eHydroxylation [Asymmetric Synthesis]\u003c\/strong\u003e — mencakup katalis dan reagen kiral yang digunakan untuk reaksi hidroksilasi asimetris, termasuk turunan alkaloid sinkona serta pasangan enansiomer oksaziridina turunan kamfer sulfonil, yang mengarahkan pembentukan pusat stereogenik baru dengan selektivitas tinggi pada substrat organik.\u003c\/p\u003e\u003cp\u003eKatalis dan reagen dalam kategori ini dipakai peneliti sintesis asimetris untuk memperkenalkan gugus hidroksil secara enantioselektif pada tahap kunci sintesis total senyawa bioaktif kompleks. Oksaziridina turunan kamfer sulfonil berperan sebagai reagen pengoksidasi kiral yang mengubah enolat menjadi alfa-hidroksi keton dengan selektivitas tinggi, sedangkan turunan sinkona seperti beta-isokupreidina dan senyawa pirolo-oksazin dipakai sebagai katalis organik pada reaksi hidroksilasi katalitik.\u003c\/p\u003e\u003cp\u003eContoh produk dalam koleksi ini: \u003ca href=\"\/en\/products\/tci2510i072835967\"\u003eTCI I0728 253430-48-7 beta-Isocupreidine\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c132615822\"\u003eTCI C1326 104322-63-6 (2R,8aS)-(+)-(Camphorylsulfonyl)oxaziridine [Asymmetric Oxidizing Reagent]\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510e097428826\"\u003eTCI E0974 1476067-44-3 (1R,3S,5R,7R,8aS)-7-Ethylhexahydro-1-(6-hydroxy-4-quinolinyl)-3,7-methano-1H-pyrrolo[2,1-c][1,4]oxazine\u003c\/a\u003e, \u003ca href=\"\/en\/products\/tci2510c132715824\"\u003eTCI C1327 104372-31-8 (2S,8aR)-(-)-(Camphorylsulfonyl)oxaziridine [Asymmetric Oxidizing Reagent]\u003c\/a\u003e.\u003c\/p\u003e\u003cp\u003ePemilihan katalis atau reagen hidroksilasi asimetris perlu disesuaikan dengan konfigurasi enansiomer yang diinginkan pada produk akhir serta kemurnian optik reagen agar hasil stereoselektif tetap konsisten. 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-building-blocks\"\u003eChiral Building Blocks\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-chiral-catalysts-chiral-ligands-chiral-reagents\"\u003eChiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-chiral-resolution-reagents\"\u003eChiral Resolution Reagents\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-chiral-resolving-reagents\"\u003eChiral Resolving Reagents\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l3-chiral-auxiliaries\"\u003eChiral Auxiliaries\u003c\/a\u003e\u003c\/li\u003e\n\u003cli\u003e\u003ca href=\"\/en\/collections\/tci-l4-proline-based-organocatalysts-asymmetric-synthesis\"\u003eProline-Based Organocatalysts [Asymmetric Synthesis]\u003c\/a\u003e\u003c\/li\u003e\n\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":"tci2510c132615822","title":"TCI C1326 104322-63-6 (2R,8aS)-(+)-(Camphorylsulfonyl)oxaziridine [Asymmetric Oxidizing Reagent]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1326 (2R,8aS)-(+)-(Camphorylsulfonyl)oxaziridine is a chiral oxidizing reagent widely used in asymmetric synthesis laboratories. Its rigid camphorsulfonyl framework directs oxygen transfer toward one face of the substrate, enabling enantioselective transformations such as the hydroxylation of enolates to α-hydroxy carbonyl compounds and the oxidation of sulfides to chiral sulfoxides. Because the reaction proceeds through neutral oxygen transfer without transition metals, it suits substrates that are sensitive to strong acids or residual metal contamination. AMI Scientific supplies this reagent in research-scale packaging for academic, pharmaceutical, and industrial research laboratories in Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":50506853843162,"sku":"TCI2510C132615822","price":1439000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1326.jpg?v=1767096757"},{"product_id":"tci2510c132715824","title":"TCI C1327 104372-31-8 (2S,8aR)-(-)-(Camphorylsulfonyl)oxaziridine [Asymmetric Oxidizing Reagent]","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eTCI C1327 (2S,8aR)-(-)-(Camphorylsulfonyl)oxaziridine is the enantiomeric counterpart of the widely used camphor-derived chiral oxidant. Its rigid sulfonyl-camphor scaffold delivers oxygen preferentially to one face of the substrate, supporting enantioselective enolate hydroxylation and the preparation of chiral sulfoxides from sulfides. The metal-free oxygen transfer mechanism is valuable when the final product must remain free of transition-metal residues. AMI Scientific offers this reagent in research-scale packaging for organic chemistry, pharmaceutical, and academic laboratories across Indonesia.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48086063349978,"sku":"TCI2510C132715824","price":2045000.0,"currency_code":"IDR","in_stock":true},{"title":"5g","offer_id":48086063382746,"sku":"TCI2510C132715825","price":6537000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510C1327.jpg?v=1767096761"},{"product_id":"tci2510e097428826","title":"TCI E0974 1476067-44-3 (1R,3S,5R,7R,8aS)-7-Ethylhexahydro-1-(6-hydroxy-4-quinolinyl)-3,7-methano-1H-pyrrolo[2,1-c][1,4]oxazine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eThis complex compound, with a chiral structure, plays a vital role in asymmetric synthesis within laboratory settings. It is a chiral reagent designed to facilitate the creation of molecules with specific stereochemical configurations. Its unique molecular architecture allows it to selectively interact with other molecules, making it a powerful tool for synthesizing compounds with precise spatial arrangements. In chemical research, this material is essential for achieving high enantioselectivity, which is crucial in the development of pharmaceuticals and other advanced chemical products.\u003c\/p\u003e\n\u003cp\u003eThe compound's chiral nature and molecular complexity make it a preferred choice for researchers aiming to control stereoselectivity in chemical reactions. Its ability to selectively interact with specific isomers enhances the efficiency and accuracy of synthetic processes. This reagent is particularly valued for its stability under standard laboratory conditions, which ensures consistent performance and ease of handling. Its reliability and effectiveness have made it a staple in both academic and industrial research environments.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, this compound is widely used by researchers in higher education institutions and research organizations. It is particularly relevant in fields such as pharmacology, organic chemistry, and industrial chemistry. Its application supports the development of new drugs and advanced chemical materials, contributing to scientific innovation and technological progress in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis in pharmaceutical research due to its ability to selectively produce enantiomers with high efficiency.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry experiments requiring precise control over stereochemistry for the synthesis of complex molecules.\u003c\/li\u003e\n\u003cli\u003eIndustrial chemical production where chiral compounds are needed for the creation of high-value products.\u003c\/li\u003e\n\u003cli\u003eDrug development projects that rely on stereoselective reactions to achieve desired pharmacological effects.\u003c\/li\u003e\n\u003cli\u003eResearch in catalytic processes where chiral reagents are essential for enhancing reaction specificity and yield.\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: 1476067-44-3\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Not specified\u003c\/li\u003e\n\u003cli\u003ePhysical form: Not specified\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from light and moisture\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eThis compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its stability and effectiveness. It is recommended to use airtight containers to prevent exposure to air and potential degradation. In laboratory settings, proper ventilation should be ensured when handling the material to minimize any risk of inhalation. Always wear appropriate personal protective equipment, such as gloves and safety goggles, when working with this compound. The material should be kept in a secure location, away from incompatible substances to ensure safe storage and handling. Regular monitoring of storage conditions is advised to maintain the integrity of the compound throughout its shelf life.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"100mg","offer_id":48086914269402,"sku":"TCI2510E097428826","price":5579000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510E0974.jpg?v=1767112088"},{"product_id":"tci2510i072835967","title":"TCI I0728 253430-48-7 beta-Isocupreidine","description":"\u003ch3\u003eDescription\u003c\/h3\u003e\n\u003cp\u003eBeta-Isocupreidine is a chiral compound widely used in asymmetric synthesis to produce molecules with specific stereochemical configurations. It serves as a key reagent or catalyst in chemical reactions that require precise control over stereochemistry. In the laboratory, it plays a crucial role in various synthetic processes, enabling the creation of complex organic structures with high enantioselectivity. Its chiral nature makes it particularly valuable in the development of pharmaceuticals and specialty chemicals.\u003c\/p\u003e\n\u003cp\u003eThe compound is known for its stability under controlled conditions and its ability to participate effectively in a range of chemical reactions. Its high purity and solid form make it ideal for use in laboratory settings where precision and reproducibility are essential. Beta-Isocupreidine is often selected for its reliability and consistent performance in synthetic protocols. Its chemical properties allow it to function as a ligand or catalyst, enhancing the efficiency of reactions such as Michael additions, aldol reactions, and enantioselective transformations.\u003c\/p\u003e\n\u003cp\u003eIn Indonesian laboratories, Beta-Isocupreidine is commonly used in organic chemistry research, especially in asymmetric synthesis and the development of new compounds. It is a preferred choice for researchers working on drug discovery, industrial chemical production, and academic studies. Its availability and performance make it a valuable tool for both academic and industrial applications in the region.\u003c\/p\u003e\n\u003ch3\u003eLaboratory Applications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eAsymmetric synthesis applications benefit from Beta-Isocupreidine’s chiral properties, enabling the selective formation of enantiomers in complex molecules.\u003c\/li\u003e\n\u003cli\u003eIn pharmaceutical research, it is used to synthesize chiral compounds with specific biological activities, supporting drug development efforts.\u003c\/li\u003e\n\u003cli\u003eFor enantioselective reactions, its ability to control stereochemistry ensures high yields of desired products in organic synthesis.\u003c\/li\u003e\n\u003cli\u003eIn industrial chemical production, it contributes to the efficient synthesis of specialty chemicals with defined stereochemistry.\u003c\/li\u003e\n\u003cli\u003eOrganic chemistry research relies on Beta-Isocupreidine for its consistent performance in catalytic and ligand-based reactions.\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eSpecifications\u003c\/h3\u003e\n\u003cul\u003e\n\u003cli\u003eBrand: TCI\u003c\/li\u003e\n\u003cli\u003eCAS number: 253430-48-7\u003c\/li\u003e\n\u003cli\u003eCategory: Chemistry \u0026gt; Asymmetric Synthesis \u0026gt; Chiral Catalysts, Chiral Ligands, Chiral Reagents\u003c\/li\u003e\n\u003cli\u003ePack sizes: Available in various quantities as per supplier specifications\u003c\/li\u003e\n\u003cli\u003ePhysical form: Solid\u003c\/li\u003e\n\u003cli\u003eStorage note: Store in a cool, dry place away from moisture and direct light\u003c\/li\u003e\n\u003c\/ul\u003e\n\u003ch3\u003eHandling and Storage\u003c\/h3\u003e\n\u003cp\u003eBeta-Isocupreidine should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep it in a sealed container to avoid exposure to moisture and air, which could affect its performance. The compound should be stored away from direct sunlight and sources of heat to ensure long-term integrity. In laboratory settings, it is important to handle it with care, using appropriate personal protective equipment such as gloves and safety goggles. While it is generally stable under normal storage conditions, it should be kept in a secure location to prevent accidental contamination or exposure. Proper storage ensures that Beta-Isocupreidine remains effective for use in synthetic processes requiring high precision and reliability.\u003c\/p\u003e","brand":"TCI","offers":[{"title":"1g","offer_id":48087412343002,"sku":"TCI2510I072835967","price":9035000.0,"currency_code":"IDR","in_stock":true}],"thumbnail_url":"\/\/cdn.shopify.com\/s\/files\/1\/0756\/7156\/8602\/files\/TCI2510I0728.jpg?v=1767120196"}],"url":"https:\/\/amiscientific.com\/en\/collections\/tci-l4-hydroxylation-asymmetric-synthesis.oembed","provider":"AMI Scientific","version":"1.0","type":"link"}