64650-34-6

Basic information

• Product Name: Benzenamine, N,N-dimethyl-3-[(4-nitrophenyl)thio]-
• CAS NO: 64650-34-6
• Molecular Formula: C14H14N2O2S
• Molecular Weight: 274.343
• Mol File: 64650-34-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzenamine, N,N-dimethyl-3-[(4-nitrophenyl)thio]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, N,N-dimethyl-3-[(4-nitrophenyl)thio]-(64650-34-6)
• EPA Substance Registry System: Benzenamine, N,N-dimethyl-3-[(4-nitrophenyl)thio]-(64650-34-6)

Safety Data

• Hazardous Substances Data: 64650-34-6(Hazardous Substances Data)

Upstream product

• 50-00-0 formaldehyd 
• 104621-64-9 3-(4-nitrophenylsulfanyl)phenylamine 
• 178752-79-9 3-(N,N-dimethylamino)phenylboronic acid 
• 1849-36-1 para-nitrobenzenethiol 
• 100-00-5 4-chlorobenzonitrile 
• 22948-02-3 3-aminothiophenol 

Relevant articles and documents

SUBSTITUTED PHENYL SULFONYL PHENYL TRIAZOLE THIONES AND USES THEREOF

The present disclosure relates to substituted phenyl sulfonyl phenyl triazole thiones, pharmaceutical compositions containing them, and methods of using them.

Copper mediated formation of carbon-heteroatom bonds using organoboron reagents and ultrasound

This report summarizes research efforts focused on copper acetate mediated reactions to form new carbon-heteroatom bonds using organoboron reagents under ultrasound irradiation. The method involves the application of ultrasound irradiation to the Chan-Evans-Lam reaction to achieve O-arylation of phenols, N-arylation of anilines and indoles, and S-arylation of thiols. Ultrasound irradiation was found to decrease reaction times from 72 hours to 4 hours while improving the product yields an average of 20%.1 Representative C-O, C-N, and C-S coupling reactions were successfully scaled-up from the milligram to gram levels while maintaining good product yields offering potential applications in industrial processes.