tert-Butyl (1R,4R,5S)-2-azabicyclo[2.2.1]heptan-5-ylcarbamate

98%

Reagent Code: #152996
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CAS Number 1932203-04-7

science Other reagents with same CAS 1932203-04-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.29 g/mol
Formula C₁₁H₂₀N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C, drying away from light

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of chiral compounds for drug discovery. Its rigid bicyclic structure and defined stereochemistry make it valuable for creating selective bioactive molecules, especially in central nervous system agents and enzyme inhibitors. The tert-butyl carbamate (Boc) group allows for easy protection and deprotection of the amine during multi-step syntheses, enhancing its utility in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿12,300.00
inventory 100mg
10-20 days ฿20,880.00
inventory 250mg
10-20 days ฿37,340.00
inventory 1g
10-20 days ฿117,600.00

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tert-Butyl (1R,4R,5S)-2-azabicyclo[2.2.1]heptan-5-ylcarbamate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of chiral compounds for drug discovery. Its rigid bicyclic structure and defined stereochemistry make it valuable for creating selective bioactive molecules, especially in central nervous system agents and enzyme inhibitors. The tert-butyl carbamate (Boc) group allows for easy protection and deprotection of the amine during multi-step syntheses, enhancing its utility in medicinal chemistry.

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of chiral compounds for drug discovery. Its rigid bicyclic structure and defined stereochemistry make it valuable for creating selective bioactive molecules, especially in central nervous system agents and enzyme inhibitors. The tert-butyl carbamate (Boc) group allows for easy protection and deprotection of the amine during multi-step syntheses, enhancing its utility in medicinal chemistry.

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