83790-89-0

Basic information

• Product Name: 4-methyl-N-(2,2,2-trichloro-1-hydroxyethyl)benzenesulfonamide
• CAS NO: 83790-89-0
• Molecular Formula: C₉H₁₀Cl₃NO₃S
• Molecular Weight: 318.6046
• Mol File: 83790-89-0.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 406.3°C at 760 mmHg
• Flash Point: 199.5°C
• Density: 1.554g/cm³
• Vapor Pressure: 2.49E-07mmHg at 25°C
• Refractive Index: 1.589
• CAS DataBase Reference: 4-methyl-N-(2,2,2-trichloro-1-hydroxyethyl)benzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methyl-N-(2,2,2-trichloro-1-hydroxyethyl)benzenesulfonamide(83790-89-0)
• EPA Substance Registry System: 4-methyl-N-(2,2,2-trichloro-1-hydroxyethyl)benzenesulfonamide(83790-89-0)

Safety Data

• Hazardous Substances Data: 83790-89-0(Hazardous Substances Data)

Upstream product

• 70-55-3 toluene-4-sulfonamide 
• 75-87-6 chloral 
• 507-47-1 1-amino-2,2,2-trichloro-ethanol 
• 98-59-9 p-toluenesulfonyl chloride 
• 473-34-7 N,N-dichloro-p-toluenesulfonamide 
• 156-60-5 trans-1,2-dichloroethylene 
• 79-01-6 Trichloroethylene 
• 83790-92-5 N-(2,2,2-trichloro-1-acetoxyethyl)-p-toluenesulfonamide 
• 51608-61-8 N-(2,2,2-trichloroethyliden)-p-toluenesulfonamide 
• 75-86-5 2-hydroxy-2-methylpropanenitrile 
• 26798-15-2 N-(2,2,2-Trichloro-1-tributylstannyloxyaethyl)toluol-p-sulfonamid 

Downstream Products

• 255048-79-4 N-[2,2,2-trichloro-1-(4-methylphenyl)ethyl]-4-methylbenzenesulfonamide 
• 786696-37-5 N-(1,2,2,2-tetrachloroethyl)-p-toluenesulfonamide 
• 26798-15-2 N-(2,2,2-Trichloro-1-tributylstannyloxyaethyl)toluol-p-sulfonamid 
• 786696-40-0 N-[2,2,2-trichloro-1-(diisopropoxyphosphoryl)ethyl]-p-toluenesulfonamide 
• 32135-55-0 1-p-Toluolsulfonamido-1-phenyl-2,2,2-trichlorethan 

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

REACTION OF TRICHLOROETHYLENE WITH N,N-DICHLOROARENESULFONAMIDES IN THE PRESENCE OF LEWIS ACIDS

The reaction of N,N-dichloroarenesulfonamides with trichloroethylene in the presence of ionic catalyst (SnCl4 and AlCl3) leads to N-(2,2,2-trichloroethyliden)-arenesulfonamides and the products of the subsequent conversion, namely, N-(2,2,2-trichloro-1-arenesulfonamidoethyl)arenesulfonamides and N-(2,2,2-trichloro-1-hydroxyethyl)arenesulfonamides.