4-Azidobenzoyl hydrazine

95%

Reagent Code: #129301
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CAS Number 63296-32-2

science Other reagents with same CAS 63296-32-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 177.16 g/mol
Formula C₇H₇N₅O
thermostat Physical Properties
Melting Point 169-170 °C
inventory_2 Storage & Handling
Storage -20°C, light-proof, inert gas

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds and pharmaceuticals. Its azide and hydrazine functional groups allow participation in click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), enabling efficient construction of triazole derivatives for drug discovery. Also employed in the development of photoaffinity probes to study biological interactions, where the azide group generates reactive nitrenes upon UV irradiation, forming covalent bonds with nearby biomolecules. Additionally, it serves in the synthesis of dyes, agrochemicals, and functional materials due to its ability to undergo cycloadditions and condensation reactions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿5,500.00
100mg
10-20 days ฿16,120.00
4-Azidobenzoyl hydrazine
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Used as a key intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds and pharmaceuticals. Its azide and hydrazine functional groups allow participation in click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), enabling efficient construction of triazole derivatives for drug discovery. Also employed in the development of photoaffinity probes to study biological interactions, where the azide group generates reactive nitrenes upon UV irr

Used as a key intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds and pharmaceuticals. Its azide and hydrazine functional groups allow participation in click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), enabling efficient construction of triazole derivatives for drug discovery. Also employed in the development of photoaffinity probes to study biological interactions, where the azide group generates reactive nitrenes upon UV irradiation, forming covalent bonds with nearby biomolecules. Additionally, it serves in the synthesis of dyes, agrochemicals, and functional materials due to its ability to undergo cycloadditions and condensation reactions.

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