884866-01-7

Basic information

• Product Name: 1-(4-methylbenzensulfonyl)-4-phenyl-1H-1,2,3-triazole
• Synonyms: 1-(4-methylbenzensulfonyl)-4-phenyl-1H-1,2,3-triazole
• CAS NO: 884866-01-7
• Molecular Weight: 299.353
• Mol File: 884866-01-7.mol
• Article Data: 69

Chemical Properties

• CAS DataBase Reference: 1-(4-methylbenzensulfonyl)-4-phenyl-1H-1,2,3-triazole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-methylbenzensulfonyl)-4-phenyl-1H-1,2,3-triazole(884866-01-7)
• EPA Substance Registry System: 1-(4-methylbenzensulfonyl)-4-phenyl-1H-1,2,3-triazole(884866-01-7)

Safety Data

• Hazardous Substances Data: 884866-01-7(Hazardous Substances Data)

Upstream product

• 941-55-9 4-toluenesulfonyl azide 
• 536-74-3 phenylacetylene 
• 504-03-0 2.6-dimethylpiperidine 
• 100-51-6 benzyl alcohol 
• 1680-44-0 4-phenyl-1H-1,2,3-triazole 
• 98-59-9 p-toluenesulfonyl chloride 
• 108-18-9 diisopropylamine 
• 623-47-2 propynoic acid ethyl ester 
• 871-84-1 1,7-Octadiyne 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 112614-96-7 4-phenyl-2H-[1,2,3]triazole 
• 102-96-5 (2-nitroethenyl)benzene 
• 1576-35-8 toluene-4-sulfonic acid hydrazide 
• 588-73-8 (Z)-β-bromostyrene 

Downstream Products

• 1680-44-0 4-phenyl-1H-1,2,3-triazole 
• 1078739-33-9 (E)-4-phenyl-2-styryl-1-tosyl-1H-imidazole 
• 1078739-39-5 4-phenyl-1-tosyl-2-((trimethylsilyl)methyl)-1H-imidazole 
• 1078739-31-7 2-heptyl-4-phenyl-1-tosyl-1H-imidazole 
• 1078739-29-3 2-(phenanthren-9-yl)-4-phenyl-1-tosyl-1H-imidazole 
• 1078739-38-4 2-(cyclohepta-2,4,6-trienyl)-4-phenyl-1-tosyl-1H-imidazole 
• 1078739-37-3 2-(4-isopropylphenyl)-4-phenyl-1-tosyl-1H-imidazole 
• 1078739-36-2 2-(4-bromophenyl)-4-phenyl-1-tosyl-1H-imidazole 
• 1078739-32-8 2-benzyl-4-phenyl-1-tosyl-1H-imidazole 
• 1078739-19-1 1-[(4-methylphenyl)sulfonyl]-2,4-diphenyl-1H-imidazole 
• 1078739-34-0 2-(4-methylphenyl)-1-[(4-methylphenyl)sulfonyl]-4-phenyl-1H-imidazole 
• 1078739-28-2 2-(4-methoxyphenyl)-1-[(4-methylphenyl)sulfonyl]-4-phenyl-1H-imidazole 
• 1078739-30-6 ethyl 2-(4-phenyl-1-tosyl-1H-imidazol-2-yl)acetate 
• 1078739-35-1 2-cyclopropyl-4-phenyl-1-tosyl-1H-imidazole 

Relevant articles and documents

Copper-catalyzed three-component cascade reaction of alkynes, sulfonyl azides and simple aldehydes/ketones

A copper-catalyzed dimethylzinc-promoted three-component cascade reaction of alkynes, sulfonyl azides, and simple aldehydes or ketones is described. Polysubstituted olefins were thus constructed expeditiously in a one-pot procedure under mild conditions.

Cycloaddition of: N -sulfonyl and N -sulfamoyl azides with alkynes in aqueous media for the selective synthesis of 1,2,3-triazoles

The cycloaddition of N-sulfonyl and N-sulfamoyl azides with terminal alkynes generally produces amide derivatives via ketenimine intermediates. We herein delineate a Cu(i) catalyzed method using a prolinamide ligand that selectively generates N-sulfonyl a

Rh-Catalyzed Formal [3+2] Cyclization for the Synthesis of 5-Aryl-2-(quinolin-2-yl)oxazoles and Its Applications in Metal Ions Probes

A facile and efficient strategy for the synthesis of 5-aryl-2-(quinolin-2-yl)oxazoles via rhodium-catalyzed formal [3+2] cyclization of 4-aryl-1-tosyl-1H-1,2,3-triazoles with quinoline-2-carbaldehydes has been described. The protocol employs mild conditions and offers good yields of diverse 2,5-aryloxazole derivatives with a broad reaction scope. It is amenable to gram-scale synthesis and easily transformation. Moreover, this 5-aryl-2-(quinolin-2-yl)oxazole skeleton is indeed a new fluorophore and its applications in metal ions probes are also investigated and showed fluorescent responses to mercury ion.

Rhodium(II)-Catalyzed [4+3] Cyclization of Triazoles with Indole Derivatives and Its Application in the Total Synthesis of (±)-Aurantioclavine

An efficient rhodium(II)-catalyzed [4+3] cyclization reaction of 1-sulfonyl-1,2-3-triazoles and indoles was developed. Azepino[5,4,3- cd]indoles, which are widely distributed in ergot alkaloids with various biological activities, could be obtained in good