(R)-Benzyl (1-aminopropan-2-yl)carbamate

95%

Reagent Code: #231422
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CAS Number 346669-50-9

science Other reagents with same CAS 346669-50-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 208.26 g/mol
Formula C₁₁H₁₆N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of beta-amino alcohols and active pharmaceutical ingredients (APIs) requiring enantiomeric purity. Its protected amine group allows for selective reactions in multi-step organic syntheses, making it valuable in drug development for cardiovascular, central nervous system, and respiratory medications. Commonly employed in asymmetric synthesis due to the stability and reactivity of the carbamate functionality.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿4,750.00
250mg
10-20 days ฿7,100.00
5g
10-20 days ฿80,010.00
1g
10-20 days ฿18,950.00
(R)-Benzyl (1-aminopropan-2-yl)carbamate
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of beta-amino alcohols and active pharmaceutical ingredients (APIs) requiring enantiomeric purity. Its protected amine group allows for selective reactions in multi-step organic syntheses, making it valuable in drug development for cardiovascular, central nervous system, and respiratory medications. Commonly employed in asymmetric synthesis due to the stability and reactivity of the carbamate functionality.<

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of beta-amino alcohols and active pharmaceutical ingredients (APIs) requiring enantiomeric purity. Its protected amine group allows for selective reactions in multi-step organic syntheses, making it valuable in drug development for cardiovascular, central nervous system, and respiratory medications. Commonly employed in asymmetric synthesis due to the stability and reactivity of the carbamate functionality.

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