1207680-79-2

Basic information

• Product Name: 4-chloro-N-[2,2,2-trichloro-1-(1-methyl-1H-pyrrol-3-yl)ethyl]benzenesulfonamide
• CAS NO: 1207680-79-2
• Molecular Weight: 402.128
• Mol File: 1207680-79-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 4-chloro-N-[2,2,2-trichloro-1-(1-methyl-1H-pyrrol-3-yl)ethyl]benzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-chloro-N-[2,2,2-trichloro-1-(1-methyl-1H-pyrrol-3-yl)ethyl]benzenesulfonamide(1207680-79-2)
• EPA Substance Registry System: 4-chloro-N-[2,2,2-trichloro-1-(1-methyl-1H-pyrrol-3-yl)ethyl]benzenesulfonamide(1207680-79-2)

Safety Data

• Hazardous Substances Data: 1207680-79-2(Hazardous Substances Data)

Upstream product

• 96-54-8 N-Methylpyrrole 
• 81924-15-4 N-(2,2,2-trichloroethylidene)-4-chlorobenzenesulfonamide 

Relevant articles and documents

C-amidoalkylation of pyrroles with N-trifluoromethylsulfonyl and N-arylsulfonyl polychloroaldehyde imines

N-(Trifluoromethylsulfonyl) and N-arylsulfonyl polychloroacetaldehyde imines reacted with pyrrole, 1-alkyl-, 1-benzyl-, and 1-(4-nitrophenyl)- substituted pyrroles, and bis-pyrroles to give the corresponding 2-[1-(sulfonylamino)polychloroethyl]-1H-pyrroles or mixtures of 2- and 3-[1-(sulfonylamino)polychloroethyl]-1H-pyrroles, depending on the nature of the Schiff base and substituent on the pyrrole nitrogen atom and reaction conditions. The first synthesis of 2,5-disubstituted NH-pyrrole by reaction of pyrrole with Schiff bases was described.