430432-26-1

Basic information

• Product Name: N-(2-chloro-phenethyl)-toluene-4-sulfonamide
• Synonyms: N-(2-chloro-phenethyl)-toluene-4-sulfonamide
• CAS NO: 430432-26-1
• Molecular Weight: 309.817
• Mol File: 430432-26-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-(2-chloro-phenethyl)-toluene-4-sulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-chloro-phenethyl)-toluene-4-sulfonamide(430432-26-1)
• EPA Substance Registry System: N-(2-chloro-phenethyl)-toluene-4-sulfonamide(430432-26-1)

Safety Data

• Hazardous Substances Data: 430432-26-1(Hazardous Substances Data)

Upstream product

• 52085-97-9 3-(2-chlorophenyl)propionyl chloride 
• 13078-80-3 2-(2-chlorophenyl)ethanamine 
• 98-59-9 p-toluenesulfonyl chloride 

Relevant articles and documents

Electrochemical C?H Amidation of Heteroarenes with N-Alkyl Sulfonamides in Aqueous Medium

The construction of C?N bonds by free radical reactions represents a powerful synthetic approach for direct C?H amidations of arenes or heteroarenes. Developing efficient and more environmentally friendly synthetic methods for C?H amidation reactions remains highly desirable. Herein, metal-free electrochemical oxidative dehydrogenative C?H amidations of heteroarenes with N-alkylsulfonamides have been accomplished. The catalyst- and chemical-oxidant-free C?H amidation features an ample scope and employs electricity as the green and sole oxidant. A variety of heteroarenes, including indoles, pyrroles, benzofuran and benzothiophene, thereby underwent this C(sp2)?H nitrogenation. Cyclic voltammetry studies and control experiments provided evidence for nitrogen-centered radicals being directly generated under metal-free electrocatalysis.