1078739-22-6

Basic information

• Product Name: 1-((4-methoxyphenyl)sulfonyl)-4-phenyl-1H-1,2,3-triazole
• Synonyms: 1-((4-methoxyphenyl)sulfonyl)-4-phenyl-1H-1,2,3-triazole
• CAS NO: 1078739-22-6
• Molecular Weight: 315.353
• Mol File: 1078739-22-6.mol
• Article Data: 14

Chemical Properties

• CAS DataBase Reference: 1-((4-methoxyphenyl)sulfonyl)-4-phenyl-1H-1,2,3-triazole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-((4-methoxyphenyl)sulfonyl)-4-phenyl-1H-1,2,3-triazole(1078739-22-6)
• EPA Substance Registry System: 1-((4-methoxyphenyl)sulfonyl)-4-phenyl-1H-1,2,3-triazole(1078739-22-6)

Safety Data

• Hazardous Substances Data: 1078739-22-6(Hazardous Substances Data)

Upstream product

• 4547-64-2 4-methoxybenzenesulfonyl azide 
• 536-74-3 phenylacetylene 

Downstream Products

• 933025-26-4 4-methoxy-N-(2-oxo-2-phenylethyl)benzenesulfonamide 
• 1394912-82-3 N-(2,2-diphenylvinyl)-4-methoxybenzenesulfonamide 
• 1078739-42-0 1-[(4-methoxyphenyl)sulfonyl]-2,4-diphenyl-1H-imidazole 
• 112614-96-7 4-phenyl-2H-[1,2,3]triazole 

Relevant articles and documents

Rhodium-Catalyzed Denitrogenative Transannulation of N-Sulfonyl-1,2,3-triazoles with Glycals Giving Pyrroline-Fused N-Glycosides

Described here is a selective synthesis of 2,3-dihydropyrrole-fused N-glycosides through rhodium-catalyzed denitrogenative transannulation of N-sulfonyl-1,2,3-triazoles with glycals. A series of pyrroline-fused N-glycosides are afforded in moderate to exc

Copper(I)-N-Heterocyclic Carbene Complexes as Efficient Catalysts for the Synthesis of 1,4-Disubstituted 1,2,3-Sulfonyltriazoles in Air

Bis-NHC and mixed NHC/PR3 copper(I) complexes (NHC = N-heterocyclic carbene) were found to be efficient catalysts enabling the azide-alkyne cycloaddition reaction leading to the formation of 1,2,3-sulfonyltriazoles under Click conditions. The mechanism of this transformation was probed and decoordination of the NHC ligand (even in the NHC/PR3 mixed ligand systems) during the catalytic transformation was observed.

Method for preparing triazole derivatives

The invention discloses a method for preparing triazole derivatives. The method comprises the following steps: taking aryl sulfonyl azide derivatives and acetylenic derivatives as raw materials, taking cuprous iodide and ortho-aminophenol as catalysts, an