4-Nitrobenzyl 1H-benzo[d][1,2,3]triazole-1-carboxylate

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Reagent Code: #39457
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CAS Number 86832-06-6

science Other reagents with same CAS 86832-06-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 298.2536 g/mol
Formula C₁₄H₁₀N₄O₄
thermostat Physical Properties
Melting Point 160-162 ℃
Boiling Point 518.4±52.0 ℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.47±0.1 g/cm3
Storage room temperature

description Product Description

This chemical is primarily utilized in organic synthesis as a protective group for hydroxyl and amine functionalities. It is particularly effective in peptide chemistry, where it helps to temporarily shield reactive groups during complex reactions, ensuring selective transformations. Additionally, it serves as a key intermediate in the development of pharmaceuticals and agrochemicals, enabling the synthesis of compounds with specific biological activities. Its nitrobenzyl group also makes it useful in photolabile applications, where it can be cleaved by light, allowing for controlled release or activation of molecules in research and industrial processes.

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Test Parameter Specification
Appearance Light Yellow Solid
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿6,822.00
inventory 1g
10-20 days ฿2,052.00

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4-Nitrobenzyl 1H-benzo[d][1,2,3]triazole-1-carboxylate
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This chemical is primarily utilized in organic synthesis as a protective group for hydroxyl and amine functionalities. It is particularly effective in peptide chemistry, where it helps to temporarily shield reactive groups during complex reactions, ensuring selective transformations. Additionally, it serves as a key intermediate in the development of pharmaceuticals and agrochemicals, enabling the synthesis of compounds with specific biological activities. Its nitrobenzyl group also makes it useful in ph

This chemical is primarily utilized in organic synthesis as a protective group for hydroxyl and amine functionalities. It is particularly effective in peptide chemistry, where it helps to temporarily shield reactive groups during complex reactions, ensuring selective transformations. Additionally, it serves as a key intermediate in the development of pharmaceuticals and agrochemicals, enabling the synthesis of compounds with specific biological activities. Its nitrobenzyl group also makes it useful in photolabile applications, where it can be cleaved by light, allowing for controlled release or activation of molecules in research and industrial processes.

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