19766-55-3

Basic information

• Product Name: N-(4-(dimethylamino)phenyl)-4-methylbenzenesulfonamide
• Synonyms: N-(4-(dimethylamino)phenyl)-4-methylbenzenesulfonamide
• CAS NO: 19766-55-3
• Molecular Weight: 290.386
• Mol File: 19766-55-3.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: N-(4-(dimethylamino)phenyl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-(dimethylamino)phenyl)-4-methylbenzenesulfonamide(19766-55-3)
• EPA Substance Registry System: N-(4-(dimethylamino)phenyl)-4-methylbenzenesulfonamide(19766-55-3)

Safety Data

• Hazardous Substances Data: 19766-55-3(Hazardous Substances Data)

Upstream product

• 99-98-9 4-amino-N,N-dimethylaniline 
• 98-59-9 p-toluenesulfonyl chloride 
• 536-57-2 p-toluene sulfinic acid 
• 138-89-6 p-dimethylaminonitrosobenzene 
• 941-55-9 4-toluenesulfonyl azide 
• 121-69-7 N,N-dimethyl-aniline 

Downstream Products

• 1616978-62-1 N-(4-(dimethylamino)phenyl)-4-methyl-N-phenylbenzenesulfonamide 
• 52373-53-2 N'-tosyl-N,N,N'-trimethyl-p-phenylenediamine 
• 52260-12-5 N-(4-Dimethylamino-phenyl)-4-methyl-N-(1-phenyl-vinyl)-benzenesulfonamide 
• 5369-34-6 N,N,N'-trimethyl-p-phenylenediamine 
• 53119-87-2 [(4-Dimethylamino-phenyl)-(toluene-4-sulfonyl)-amino]-phenyl-acetic acid methyl ester 
• 53119-89-4 N-(4-Dimethylamino-phenyl)-N-(2-hydroxy-1-phenyl-ethyl)-4-methyl-benzenesulfonamide 

Relevant articles and documents

Cs2CO3 catalyzed rapid and efficient conversion of amines into sulfonamides; Alcohols and phenols into sulfonic esters

A simple and efficient method has been developed for the sulfonylation of several amines, alcohols, and phenols by p-toluenesulphonylchloride (p-TsCl) in the presence of catalytic amount of Cs2CO3 at 25C to obtain sulfonamides and sulfonic esters in very good yields. Cs2CO3 has been found to be highly efficient catalyst. Taylor & Francis Group, LLC.

Chemical and electrochemical oxidative coupling of N,N-dialkyl-p- phenylenediamines and arylsulfinic acids. Synthesis of sulfonamide derivatives

Electrochemical and chemical oxidation of N,N-dialkyl-p-phenylenediamines have been studied in the presence of arylsulfinic acids as nucleophiles in aqueous solutions for the synthesis of sulfonamide derivatives. The results indicate that the electrochemi

A simple and efficient method for sulfonylation of amines, alcohols and phenols with cupric oxide under mild conditions

Cupric Oxide efficiently catalyzed the synthesis of sulfonamides and sulfonic esters. This method has been applied to a variety of substrates including nucleophilic and sterically-hindered amines, alcohols and phenols with excellent yields of sulfonamides and sulfonic esters. The remarkable selectivity under mild and neutral conditions of this commercially available inexpensive catalyst is an attractive feature of this method.