1402745-49-6

Basic information

• Product Name: ethyl 2-phenyl-6-(trifluoromethyl)quinoline-1(2H)-carboxylate
• Synonyms: ethyl 2-phenyl-6-(trifluoromethyl)quinoline-1(2H)-carboxylate
• CAS NO: 1402745-49-6
• Molecular Weight: 347.337
• Mol File: 1402745-49-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: ethyl 2-phenyl-6-(trifluoromethyl)quinoline-1(2H)-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-phenyl-6-(trifluoromethyl)quinoline-1(2H)-carboxylate(1402745-49-6)
• EPA Substance Registry System: ethyl 2-phenyl-6-(trifluoromethyl)quinoline-1(2H)-carboxylate(1402745-49-6)

Safety Data

• Hazardous Substances Data: 1402745-49-6(Hazardous Substances Data)

Upstream product

• 3262-89-3 triphenylboroxine 
• 1402745-48-5 6-trifluoromethyl-N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline 
• 455-14-1 4-trifluoromethylphenylamine 
• 325-13-3 6-(trifluoromethyl) quinolone 

Relevant articles and documents

Mechanistic investigation of the nickel-catalyzed Suzuki reaction of N, O-acetals: Evidence for boronic acid assisted oxidative addition and an iminium activation pathway

The mechanism of a recently reported Suzuki coupling reaction of quinoline-derived allylic N,O-acetals has been studied using a combination of structural, stereochemical, and kinetic isotope effect experiments. The data indicate that C-O activation is fac