77826-10-9

Basic information

• Product Name: N-Phenyl-N-(3-trifluoromethyl-phenyl)-benzamide
• Synonyms: N-Phenyl-N-(3-trifluoromethyl-phenyl)-benzamide
• CAS NO: 77826-10-9
• Molecular Weight: 341.332
• Mol File: 77826-10-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-Phenyl-N-(3-trifluoromethyl-phenyl)-benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-Phenyl-N-(3-trifluoromethyl-phenyl)-benzamide(77826-10-9)
• EPA Substance Registry System: N-Phenyl-N-(3-trifluoromethyl-phenyl)-benzamide(77826-10-9)

Safety Data

• Hazardous Substances Data: 77826-10-9(Hazardous Substances Data)

Upstream product

• 101-23-5 N-(3-trifluoromethylphenyl)aniline 
• 98-88-4 benzoyl chloride 

Downstream Products

• 101-23-5 N-(3-trifluoromethylphenyl)aniline 
• 65-85-0 benzoic acid 

Relevant articles and documents

Micellar Catalysis of the Basic Hydrolysis of Amides. 4. Substituted N,N-Diphenylbenzamides

The cytalysis of the basic hydrolysis of a series of N-aryl-N-phenylbenzamides (1) and a series of substituted N,N-diphenylbenzamides (2) by micelles of cetyltrimethylammonium bromide (ctab) has been studied.On the basis of the effects of substituents on the aromatic ring attached to the nitrogen atom, a mechanistic change on transfer from water to a micellar environment is proposed.In water the mechanism involves rate-determining solvent-assisted carbon-nitrogen bond breaking (mechanism B), while in the presence of micelles of ctab, a rate-determining attack of hydroxide ion (mechanism C) is proposed.Reasons for mechanistic change are discussed.