tert-Butyl(2-hydroxybutyl)(methyl)carbamate

98%

Reagent Code: #155554
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CAS Number 1889077-30-8

science Other reagents with same CAS 1889077-30-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.28 g/mol
Formula C₁₀H₂₁NO₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its hydroxyl and carbamate functional groups allow for selective modifications, making it valuable in building complex molecules. Commonly employed in the development of protected amino alcohols, it serves as a building block in medicinal chemistry for synthesizing bioactive compounds. The tert-butyl carbamate group acts as a protecting group for amines, enabling controlled reaction sequences in multi-step syntheses. Its stability under various reaction conditions and ease of deprotection enhance its utility in drug discovery and process chemistry.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿9,560.00
1g
10-20 days ฿34,060.00
5g
10-20 days ฿51,970.00
250mg
10-20 days ฿13,650.00
10g
10-20 days ฿92,470.00
tert-Butyl(2-hydroxybutyl)(methyl)carbamate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its hydroxyl and carbamate functional groups allow for selective modifications, making it valuable in building complex molecules. Commonly employed in the development of protected amino alcohols, it serves as a building block in medicinal chemistry for synthesizing bioactive compounds. The tert-butyl carbamate group acts as a protecting group for amines, enabling controlled reaction sequen

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its hydroxyl and carbamate functional groups allow for selective modifications, making it valuable in building complex molecules. Commonly employed in the development of protected amino alcohols, it serves as a building block in medicinal chemistry for synthesizing bioactive compounds. The tert-butyl carbamate group acts as a protecting group for amines, enabling controlled reaction sequences in multi-step syntheses. Its stability under various reaction conditions and ease of deprotection enhance its utility in drug discovery and process chemistry.

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