17798-15-1

Basic information

• Product Name: Benzenesulfonamide, N-(2-chloro-1-phenylethyl)-4-methyl-
• Synonyms: N-<2-Chlor-1-phenylethyl>-p-toluolsulfonamid;2-chloro-1-phenyl-N-tosylethanamine
• CAS NO: 17798-15-1
• Molecular Formula: C15H16ClNO2S
• Molecular Weight: 309.817
• Mol File: 17798-15-1.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: Benzenesulfonamide, N-(2-chloro-1-phenylethyl)-4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonamide, N-(2-chloro-1-phenylethyl)-4-methyl-(17798-15-1)
• EPA Substance Registry System: Benzenesulfonamide, N-(2-chloro-1-phenylethyl)-4-methyl-(17798-15-1)

Safety Data

• Hazardous Substances Data: 17798-15-1(Hazardous Substances Data)

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 20989-17-7 Phenylglycinol 
• 24395-14-0 N-(p-tolylsulfonyl)-2-phenylaziridine 
• 100-42-5 styrene 
• 127-65-1 chloroamine-T 
• 593-71-5 Chloroiodomethane 
• 51608-60-7 N-(benzylidene)-p-methylbenzenesulfonamide 
• 622-24-2 2-phenylethyl chloride 
• 70-55-3 toluene-4-sulfonamide 
• 473-34-7 N,N-dichloro-p-toluenesulfonamide 

Relevant articles and documents

A phosphonium ylide as a visible light organophotoredox catalyst

A phosphonium ylide-based visible light organophotoredox catalyst has been designed and successfully applied to halohydrin synthesis using trichloroacetonitrile and epoxides. An oxidative quenching cycle by the ylide catalyst was established, which was confirmed by experimental mechanistic studies.

A versatile metal-free intermolecular aminochlorination of alkenes

New reaction conditions for the rapid and productive intermolecular aminochlorination reaction of alkenes using a combination of chloramine-T and a Br?nstedt acid are described. Upon simple protonation of chloramine-T, conditions for a mild and selective aminochlorination are obtained. In addition, the reaction can proceed to form either of the two possible regioisomers, depending on whether a stoichiometric amount of such an acid activator or acetic acid is used as solvent. The reaction is operative for all different classes of alkenes. A total of over 50 examples is presented to illustrate this concept.

Hydrated nickel (II) halides mediated ring opening reaction with N-tosylaziridines

An efficient and water tolerant method for the synthesis of β-haloamines is described utilizing hydrated nickel (II) halides (NiX 2·nH2O X = Cl, Br, I) and aziridines as starting materials. N-Tosylaziridines reacted with NiCl2/