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1H-1,2,3-Triazole, 4-(azidophenylmethyl)-5-phenyl- is a complex organic compound with the molecular formula C15H12N6. It is a derivative of 1,2,3-triazole, a five-membered heterocyclic ring containing three nitrogen atoms. The compound features an azidophenylmethyl group attached to the 4-position of the triazole ring and a phenyl group at the 5-position. This chemical is known for its unique reactivity and stability, making it a valuable building block in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its azide functionality can participate in click chemistry reactions, which are highly efficient and specific, allowing for the formation of new bonds under mild conditions. The compound's structure and properties make it a promising candidate for applications in materials science, medicinal chemistry, and other fields where the creation of new, stable, and functional molecules is desired.

88596-66-1

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88596-66-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88596-66-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,5,9 and 6 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 88596-66:
(7*8)+(6*8)+(5*5)+(4*9)+(3*6)+(2*6)+(1*6)=201
201 % 10 = 1
So 88596-66-1 is a valid CAS Registry Number.

88596-66-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[azido(phenyl)methyl]-5-phenyl-2H-triazole

1.2 Other means of identification

Product number -
Other names 1H-1,2,3-Triazole,4-(azidophenylmethyl)-5-phenyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:88596-66-1 SDS

88596-66-1Upstream product

88596-66-1Downstream Products

88596-66-1Relevant academic research and scientific papers

APPROACHES TOWARDS THE SYNTHESIS OF ALLENYL AZIDES

L'abbe, Gerrit,Mahy, Michel,Bollyn, Marcus,Germain, Gabriel,Scheefer, Guy

, p. 881 - 892 (2007/10/02)

Methods which are known to produce allenes under mild conditions have failed to synthesize the yet unknown title compounds.These are (i) azide substitution of propargyl sulfonates, (ii) reactions of α-azido acid chlorides with ynamines, and (iii) Wittig condensation of α-azido acid chlorides with phosphorus ylides.The reaction products obtained are respectively azidoalkyl-1,2,3-triazoles (4), pyrrolinones (6) or pyridines (8), and a disubstituted ylide (11) or the fused triazole 12.

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