1427026-26-3

Basic information

• Product Name: 1-(4-methylbenzenesulfonyl)-4-(4-fluorobenzene)-1H-1,2,3-triazole
• Synonyms: 1-(4-methylbenzenesulfonyl)-4-(4-fluorobenzene)-1H-1,2,3-triazole
• CAS NO: 1427026-26-3
• Molecular Weight: 317.344
• Mol File: 1427026-26-3.mol
• Article Data: 24

Chemical Properties

• CAS DataBase Reference: 1-(4-methylbenzenesulfonyl)-4-(4-fluorobenzene)-1H-1,2,3-triazole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-methylbenzenesulfonyl)-4-(4-fluorobenzene)-1H-1,2,3-triazole(1427026-26-3)
• EPA Substance Registry System: 1-(4-methylbenzenesulfonyl)-4-(4-fluorobenzene)-1H-1,2,3-triazole(1427026-26-3)

Safety Data

• Hazardous Substances Data: 1427026-26-3(Hazardous Substances Data)

Upstream product

• 115665-76-4 (Z)-1-(2-bromovinyl)-4-fluorobenzene 
• 766-98-3 1-ethynyl-4-fluorobenzene 
• 941-55-9 4-toluenesulfonyl azide 

Downstream Products

• 1427026-31-0 1-(4-(4-fluorophenyl)-2-methyl-1-tosyl-1H-pyrrol-3-yl)propan-2-one 
• 1598463-56-9 N-(2-(4-(diethylamino)phenyl)-2-(4-fluorophenyl)vinyl)-4-methylbenzenesulfonamide 
• 1598463-55-8 N-(2-(4-(diethylamino)phenyl)-2-(4-fluorophenyl)vinyl)-4-methylbenzenesulfonamide 
• 1613045-76-3 (Z)-N-(1-(dimethylamino)-3-(4-fluorophenyl)-3-oxo-1-phenylprop-1-en-2-yl)-4-methylbenzenesulfonamide 
• 1613045-77-4 C₂₄H₂₃FN₂O₃S 

Relevant articles and documents

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