380389-65-1

Basic information

• Product Name: Benzamide, 4-chloro-N-[2-(1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl]-
• Synonyms: T0503-6966;Benzamide,4-chloro-N-[2-(1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl];1-(4-chlorophenylcarboxamido)-2-(1H-1-imidazolyl)-5-trifluoromethylbenzene
• CAS NO: 380389-65-1
• Molecular Formula: C17H11ClF3N3O
• Molecular Weight: 365.73700
• Mol File: 380389-65-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzamide, 4-chloro-N-[2-(1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, 4-chloro-N-[2-(1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl]-(380389-65-1)
• EPA Substance Registry System: Benzamide, 4-chloro-N-[2-(1H-imidazol-1-yl)-5-(trifluoromethyl)phenyl]-(380389-65-1)

Safety Data

• Hazardous Substances Data: 380389-65-1(Hazardous Substances Data)

Upstream product

• 25373-61-9 1-(2-nitro-4-trifluoromethylphenyl)-1H-imidazole 
• 121-17-5 2-chloro-3-nitro-5-trifluoromethylbenzene 
• 122-01-0 4-chloro-benzoyl chloride 
• 380389-67-3 2-(1H-imidazol-1-yl)-5-(trifluoromethyl)aniline 

Downstream Products

• 380420-01-9 5-(4-chlorobenzoyl)-4-morpholino-4-thioxo-7-trifluoromethyl-4,5-dihydrobenzo[e]imidazo[2,1-c][1,4,2]diazaphosphinine 
• 420849-27-0 5-(4-chlorobenzoyl)-4-bromo-7-trifluoromethyl-4,5-dihydrobenzo[e]imidazo[2,1-c][1,4,2]diazaphosphinine 
• 420849-29-2 5-(4-chlorobenzoyl)-4-phenyl-7-trifluoromethyl-4,5-dihydrobenzo[e]imidazo[2,1-c][1,4,2]diazaphosphinine 

Relevant articles and documents

Synthesis and properties of 4,5-dihydrobenzo[e]imidazo[2,1-c][1,4,2]diazaphosphinine derivatives

A number of 4,5-dihydrobenzo[e]imidazo[2,1-c][1,4,2]diazaphosphinine derivatives were prepared by the direct phosphorylation of 1-(4-Chloro-phenylcarboxamido)-2-(1H-1-imidazolyl)-5-trifluoromethylbenzene in basic medium with phosphorus(III) bromide and dibromophenylphosphine. The amide was reacted with phosphorus(III) bromide to yield the tricyclic compound. The tricyclic compound with a trivalent phosphorus atom went through the diazaphosphine ring opening upon treatment with secondary amines in the presence of sulphur.