tert-butyl(3R,5S)-3-amino-5-methylpiperidine-1-carboxylate-A29748

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Reagent Code: #228707
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CAS Number 1860012-52-7

science Other reagents with same CAS 1860012-52-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.3 g/mol
Formula C₁₁H₂₂N₂O₂
badge Registry Numbers
MDL Number MFCD28368518
inventory_2 Storage & Handling
Storage 2-8°C, dry, light-proof

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors and antidiabetic drugs. Its stereochemistry enables selective interactions in biological systems, enhancing drug efficacy and reducing side effects. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Suitable for use in coupling reactions and multistep organic syntheses where controlled amine functionality is needed.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,230.00
inventory 500mg
10-20 days ฿24,710.00

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tert-butyl(3R,5S)-3-amino-5-methylpiperidine-1-carboxylate-A29748
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Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors and antidiabetic drugs. Its stereochemistry enables selective interactions in biological systems, enhancing drug efficacy and reducing side effects. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Suitable for use in coupling reactions and multistep organic syntheses where controlled amine functionality is ne

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors and antidiabetic drugs. Its stereochemistry enables selective interactions in biological systems, enhancing drug efficacy and reducing side effects. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Suitable for use in coupling reactions and multistep organic syntheses where controlled amine functionality is needed.

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