1342899-83-5

Basic information

• Product Name: N,N-dibenzyl-4-[3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide
• Synonyms: N,N-dibenzyl-4-[3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide
• CAS NO: 1342899-83-5
• Molecular Weight: 471.503
• Mol File: 1342899-83-5.mol

Chemical Properties

• CAS DataBase Reference: N,N-dibenzyl-4-[3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-dibenzyl-4-[3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide(1342899-83-5)
• EPA Substance Registry System: N,N-dibenzyl-4-[3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide(1342899-83-5)

Safety Data

• Hazardous Substances Data: 1342899-83-5(Hazardous Substances Data)

Upstream product

• 103-49-1 dibenzylamine 
• 98-61-3 p-Iodobenzenesulfonyl chloride 
• 428486-70-8 N,N-dibenzyl-p-iodobenzenesulfonamide 
• 20154-03-4 3-(trifluoromethyl)pyrazole 

Downstream Products

• 169590-42-5 4-[5-(4-(methyl)phenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulphonamide 
• 853793-24-5 N,N-dibenzyl-4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide 

Relevant articles and documents

A novel three-step synthesis of Celecoxib via palladium-catalyzed direct arylation

A novel three linear step synthesis of Celecoxib was achieved in 33% overall yield via a key regioselective direct C-H arylation reaction between a 1,3-disubstituted pyrazole and an aryl bromide.

Efficient copper-catalyzed cross-coupling of nitrogen nucleophiles with N,N-dibenzyl-4-iodobenzenesulfonamide and its application in the synthesis of Celecoxib intermediate

A practical and efficient strategy has been developed for the cross-coupling of N,N-dibenzyl-4-iodobenzenesulfonamide with nitrogen nucleophiles using 0.5–20 mol% of CuI under ligand-free conditions. A variety of nitrogen nucleophiles including nitrogen h