360564-14-3

Basic information

• Product Name: Benzenesulfonamide, 4-chloro-N-(2,2-dichloro-1-hydroxy-2-phenylethyl)-
• CAS NO: 360564-14-3
• Molecular Formula: C14H12Cl3NO3S
• Molecular Weight: 380.679
• Mol File: 360564-14-3.mol

Chemical Properties

• CAS DataBase Reference: Benzenesulfonamide, 4-chloro-N-(2,2-dichloro-1-hydroxy-2-phenylethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonamide, 4-chloro-N-(2,2-dichloro-1-hydroxy-2-phenylethyl)-(360564-14-3)
• EPA Substance Registry System: Benzenesulfonamide, 4-chloro-N-(2,2-dichloro-1-hydroxy-2-phenylethyl)-(360564-14-3)

Safety Data

• Hazardous Substances Data: 360564-14-3(Hazardous Substances Data)

Upstream product

• 1329689-03-3 4-chloro-N-[2,2-dichloro-1-(4-chlorophenoxy)-2-phenylethyl]benzenesulfonamide 
• 17260-65-0 N,N-dichloro-4-chlorobenzenesulfonamide 
• 536-74-3 phenylacetylene 
• 98416-35-4 N-(2-benzene-2,2-dichloroethylidene)-4-chlorobenzenesulfonamide 
• 75-86-5 2-hydroxy-2-methylpropanenitrile 
• 71-43-2 benzene 

Downstream Products

• 360564-12-1 1,1-dichloro-2,2-bis(4-chlorophenylsulfonylamino)-1-phenylethane 
• 1309880-85-0 4-chloro-N-(2,2-dichloro-2-phenylethyl)benzenesulfonamide 
• 429619-19-2 N-[2,2-dichloro-1-(4-methylphenyl)-2-phenylethyl]-4-chlorobenzenesulfonamide 
• 5021-43-2 2-phenylquinoxaline 

Relevant articles and documents

New approach to the preparation of p-(1-cyanoethyl)arenesulfonamides by reaction of arylsulfonyl imines of polychloroacetaldehydes with acetone cyanohydrin

Reaction of N-(2,2,2-trichloroethylidene)- or N-(1-phenyl-2,2-dichloroethylidene)arenesulfonamides with acetone cyanohydrin in acetone in the presence of potassium carbonate led to the formation of N- (2,2,2-trichloro-1-cyanoethyl)- or N-(2-phenyl-2,2-dic

A new synthesis of 3-(sulfonamido)benzofurans through an acid-promoted cascade reaction of N-(2,2-dichloro-2-phenylethylidene)arenesulfonamides with para-substituted phenols

2-Phenyl-3-(sulfonamido)benzofurans are produced in a cascade reaction of N-(2,2-dichloro-2-phenylethylidene)arenesulfonamides with para-substituted phenols in the presence of the superacid H2SO4/P 4O10 system. A convenient synthetic approach to 2-aryl-3-(sulfonamido)benzofurans through a cascade reaction of available N-(2,2-dichloro-2-phenylethylidene)arenesulfonamides withpara-substituted phenols in the presence of the superacid H2SO4/P 4O10 system was developed.

Reactions of N-(2,2-dichloro-2-phenylethylidene)arenesulfonamicles with aromatic and heterocyclic compounds

Benzene, toluene, and 2-chlorothiophene regioselectively react with N-(2,2-dichloro-2-phenylethylidene)arenesulfonamides in the presence of oleum to give N-[1-aryl(or hetaryl)-2,2-dichloro-2-phenylethyl]arenesulfonamides. Analogous C-amidoalkylation products are formed by the action of N-(2,2-dichloro-1-hydroxy-2-phenylethyl)- and N-(1-arylsulfonylamino-2,2-dichloro-2-phenylethyl)arenesulfonamides on toluene and 2-chlorothiophene in concentrated sulfuric acid.

Synthesis of N-(2-benzene-2,2-dichloroethylidene)-4-chlorobenzenesulfonamide and N-(2-benzene-2,2-dichloroethylidene)-4-methylbenzenesulfonamide

In reaction of N,N-dichloro-4-chlorobenzene-and N,N-dichloro-4-methylbenzenesulfonamides with phenylacetylene were obtained in good yield N-(2-benzene-2,2-dichloroethylidene)arenesulfonamides. The latter undergo nucleophilic addition of water, ethanol, an