1612790-52-9

Basic information

• Product Name: (5-methyl-1-phenyl-1H-1,2,3-triazol-4-yl)(p-tolyl)methanone
• Synonyms: (5-methyl-1-phenyl-1H-1,2,3-triazol-4-yl)(p-tolyl)methanone
• CAS NO: 1612790-52-9
• Molecular Weight: 277.326
• Mol File: 1612790-52-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (5-methyl-1-phenyl-1H-1,2,3-triazol-4-yl)(p-tolyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (5-methyl-1-phenyl-1H-1,2,3-triazol-4-yl)(p-tolyl)methanone(1612790-52-9)
• EPA Substance Registry System: (5-methyl-1-phenyl-1H-1,2,3-triazol-4-yl)(p-tolyl)methanone(1612790-52-9)

Safety Data

• Hazardous Substances Data: 1612790-52-9(Hazardous Substances Data)

Upstream product

• 130649-66-0 1-(4-Methylphenyl)-3-buten-1-one 
• 622-37-7 Phenyl azide 

Relevant articles and documents

A NHC-catalyzed 1,3-dipolar cycloaddition reaction of allyl ketones with azides: Direct access to 1,4,5-trisubstituted 1,2,3-triazoles

A NHC-catalyzed 1,3-dipolar cycloaddition reaction of allyl ketones with azides has been developed. This strategy could generate 1,4,5-trisubstituted 1,2,3-triazoles in high yields and regioselectivities in the presence of a 20 mol% N-heterocyclic carbene catalyst. A broad substrate scope of this process is also presented.

Direct access to 1,2,3-triazoles through organocatalytic 1,3-dipolar cycloaddition reaction of allyl ketones with azides

A general organocatalytic 1,3-dipolar cycloaddition reaction between allyl ketones and various azides is reported. The reaction is catalyzed by a secondary amine to generate substituted 1,2,3-triazoles with high levels of regioselectivity. This journal is the Partner Organisations 2014.