75040-61-8

Basic information

• Product Name: Benzenamine, N-(1-phenylethylidene)-2-(trifluoromethyl)-
• CAS NO: 75040-61-8
• Molecular Formula: C15H12F3N
• Molecular Weight: 263.262
• Mol File: 75040-61-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzenamine, N-(1-phenylethylidene)-2-(trifluoromethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenamine, N-(1-phenylethylidene)-2-(trifluoromethyl)-(75040-61-8)
• EPA Substance Registry System: Benzenamine, N-(1-phenylethylidene)-2-(trifluoromethyl)-(75040-61-8)

Safety Data

• Hazardous Substances Data: 75040-61-8(Hazardous Substances Data)

Upstream product

• 98-86-2 acetophenone 
• 88-17-5 2-(trifluoromethyl)benzenamine 
• 74653-65-9 N?sulfinyl?2?trifluoromethylaniline 

Downstream Products

• 128924-99-2 N-isopropyl-2-phenylquinolin-4-amine 
• 128925-04-2 N,N'-Diisopropyl-2-[1-phenyl-eth-(E)-ylideneamino]-benzamidine 
• 1144-20-3 2-phenyl-4-quinolinol 
• 137434-53-8 N,N'-bis<3-(dimethylamino)propyl>-2-<(1-phenylethylidene)amino>benzamidine 
• 128925-09-7 [1-Phenyl-eth-(E)-ylidene]-[2-(1,4,5,6-tetrahydro-pyrimidin-2-yl)-phenyl]-amine 
• 6725-13-9 2-amino-N-<2-(dimethylamino)ethyl>benzamide 
• 148726-12-9 N-<2-(Dimethylamino)ethyl>-2-phenylquinolin-4-amine 
• 128924-97-0 Diisopropyl-(2-phenyl-quinolin-4-yl)-amine 
• 22680-63-3 4-ethoxy-2-phenylquinoline 
• 189877-75-6 4-(1,1,1,3,3,3-Hexamethyl-disilazan-2-yl)-2-phenyl-quinoline 
• 128924-95-8 N-(tert-butyl)-2-phenylquinolin-4-amine 
• 128924-96-9 N,N'-Di-tert-butyl-2-[1-phenyl-eth-(E)-ylideneamino]-benzamidine 
• 128924-98-1 4-tert-Butoxy-2-phenyl-quinoline 

Relevant articles and documents

QUINOLINES DERIVATIVES AS NOVEL ANTICANCER AGENTS

The invention provides quinoline derivatives, their manufacture, pharmaceutical compositions containing them, and their use as medicaments. The active compounds of the present invention are useful for the treatment of proliferative neoplastic and nonneoplastic diseases.

Monomeric Metaphosphate Anion: Reaction with Carbonyl Groups

The elusive monomeric metaphosphate anion is generated rapidly at room temperature by the fragmentation of threo- or erythro- (1,2-dibromo-1-phenylpropyl)phosphonate in the presence of a hindered base; it reacts at the carbonyl groups of acetophenone and