4937-54-6

Basic information

• Product Name: (4-chlorophenyl)(2-(methylamino)phenyl)methanone
• Synonyms: (4-chlorophenyl)(2-(methylamino)phenyl)methanone
• CAS NO: 4937-54-6
• Molecular Weight: 245.708
• Mol File: 4937-54-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (4-chlorophenyl)(2-(methylamino)phenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (4-chlorophenyl)(2-(methylamino)phenyl)methanone(4937-54-6)
• EPA Substance Registry System: (4-chlorophenyl)(2-(methylamino)phenyl)methanone(4937-54-6)

Safety Data

• Hazardous Substances Data: 4937-54-6(Hazardous Substances Data)

Upstream product

• 2894-51-1 2-amino-4'-chlorobenzophenone 
• 614-00-6 N-methyl-N-nitrosoaniline 
• 106-43-4 para-chlorotoluene 
• 100-61-8 N-methylaniline 
• 74-88-4 methyl iodide 

Downstream Products

• 58658-41-6 3-chloro-10-methylacridin-9(10H)-one 
• 1610460-77-9 3-benzyl-3-(4-chlorophenyl)-1-methylindolin-2-one 
• 42259-84-7 2-chloro-10-methylacridine-9(10H)-one 

Relevant articles and documents

Transition-Metal-Free Synthesis of Acridones via Base-Mediated Intramolecular Oxidative C?H Amination

Intramolecular oxidative C?H amination of 2-aminobenzophenones was achieved in the presence of potassium tert-butoxide and dimethyl sulfoxide. A series of functionalized acridones were prepared in moderate to excellent yields in a mild, efficient, and transition-metal-free manner. (Figure presented.).

Palladium-catalyzed oxidative C-H bond acylation of N-nitrosoanilines with toluene derivatives: A traceless approach to synthesize N-alkyl-2-aminobenzophenones

A palladium-catalyzed cascade cross-coupling of N-nitroso-anilines and toluene derivatives for the direct synthesis of N-alkyl-2-aminobenzophenones is described. N-nitroso groups in anilines can act as the traceless directing groups while toluene derivatives can serve as effective acyl precursors under mild reaction conditions.