(R)-tert-Butyl (oXnran-2-ylmethyl)carbamate

98%

Reagent Code: #231129
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CAS Number 149057-20-5

science Other reagents with same CAS 149057-20-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 173.21 g/mol
Formula C₈H₁₅NO₃
badge Registry Numbers
MDL Number MFCD11111972
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role. Its protected amine group allows for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of bioactive molecules, including protease inhibitors and central nervous system agents. The tert-butyl carbamate (Boc) group provides stability under various reaction conditions and can be easily removed under mild acidic conditions, making it ideal for use in peptide chemistry and medicinal chemistry research.

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Test Parameter Specification
Appearance Solid
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,310.00
inventory 250mg
10-20 days ฿14,830.00
inventory 1g
10-20 days ฿46,680.00
(R)-tert-Butyl (oXnran-2-ylmethyl)carbamate
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role. Its protected amine group allows for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of bioactive molecules, including protease inhibitors and central nervous system agents. The tert-butyl carbamate (Boc) group provides stability under various reaction conditions and can be ea

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role. Its protected amine group allows for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of bioactive molecules, including protease inhibitors and central nervous system agents. The tert-butyl carbamate (Boc) group provides stability under various reaction conditions and can be easily removed under mild acidic conditions, making it ideal for use in peptide chemistry and medicinal chemistry research.

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