tert-Butyl 4-nitrobenzylcarbamate

≥95%

Reagent Code: #121418
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CAS Number 94838-58-1

science Other reagents with same CAS 94838-58-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.27 g/mol
Formula C₁₂H₁₆N₂O₄
badge Registry Numbers
MDL Number MFCD09038178
thermostat Physical Properties
Boiling Point 408.8°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This chemical is primarily utilized in organic synthesis as a protective group for amines. It is often employed in peptide synthesis to safeguard the amine functionality during reactions, ensuring selective modification of other functional groups. The nitrobenzyl group can be removed under mild conditions, making it suitable for sensitive applications. Additionally, it serves as an intermediate in the preparation of pharmaceuticals and agrochemicals, where controlled release or protection of amine groups is critical. Its stability and ease of deprotection make it a valuable tool in complex synthetic pathways.

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Test Parameter Specification
Appearance White To Off-White To Yellow To Light Green Powder Or Crystals
Purity (%) 94.5-100%
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿910.00
inventory 1g
10-20 days ฿1,800.00
inventory 5g
10-20 days ฿5,720.00

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tert-Butyl 4-nitrobenzylcarbamate
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This chemical is primarily utilized in organic synthesis as a protective group for amines. It is often employed in peptide synthesis to safeguard the amine functionality during reactions, ensuring selective modification of other functional groups. The nitrobenzyl group can be removed under mild conditions, making it suitable for sensitive applications. Additionally, it serves as an intermediate in the preparation of pharmaceuticals and agrochemicals, where controlled release or protection of amine groups

This chemical is primarily utilized in organic synthesis as a protective group for amines. It is often employed in peptide synthesis to safeguard the amine functionality during reactions, ensuring selective modification of other functional groups. The nitrobenzyl group can be removed under mild conditions, making it suitable for sensitive applications. Additionally, it serves as an intermediate in the preparation of pharmaceuticals and agrochemicals, where controlled release or protection of amine groups is critical. Its stability and ease of deprotection make it a valuable tool in complex synthetic pathways.

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