tert-Butyl (4-aminophenyl)carbamate

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Reagent Code: #145864
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CAS Number 71026-66-9

science Other reagents with same CAS 71026-66-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 208.26 g/mol
Formula C₁₁H₁₆N₂O₂
thermostat Physical Properties
Melting Point 113°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for the protection of amino groups during peptide synthesis. Its primary application lies in the preparation of protected aniline derivatives, which are key building blocks in the development of active pharmaceutical ingredients (APIs). The tert-butyloxycarbonyl (Boc) group allows for selective protection of the amine functionality, enabling multi-step syntheses under mild conditions. It is also employed in the production of dyes, agrochemicals, and specialty polymers where controlled reactivity of the amine group is required. The compound’s stability and ease of deprotection make it valuable in combinatorial chemistry and drug discovery processes.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿380.00
inventory 5g
10-20 days ฿810.00
inventory 100g
10-20 days ฿14,110.00
inventory 25g
10-20 days ฿3,550.00

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tert-Butyl (4-aminophenyl)carbamate
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Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for the protection of amino groups during peptide synthesis. Its primary application lies in the preparation of protected aniline derivatives, which are key building blocks in the development of active pharmaceutical ingredients (APIs). The tert-butyloxycarbonyl (Boc) group allows for selective protection of the amine functionality, enabling multi-step syntheses under mild conditions. It is also employed in the prod

Used as an intermediate in organic synthesis, particularly in the pharmaceutical industry for the protection of amino groups during peptide synthesis. Its primary application lies in the preparation of protected aniline derivatives, which are key building blocks in the development of active pharmaceutical ingredients (APIs). The tert-butyloxycarbonyl (Boc) group allows for selective protection of the amine functionality, enabling multi-step syntheses under mild conditions. It is also employed in the production of dyes, agrochemicals, and specialty polymers where controlled reactivity of the amine group is required. The compound’s stability and ease of deprotection make it valuable in combinatorial chemistry and drug discovery processes.

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