1499198-35-4

Basic information

• Product Name: 4,4,4-trifluoro-1-(furan-2-yl)-3-phenylbutan-1-one
• Synonyms: 4,4,4-trifluoro-1-(furan-2-yl)-3-phenylbutan-1-one
• CAS NO: 1499198-35-4
• Molecular Weight: 268.235
• Mol File: 1499198-35-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4,4,4-trifluoro-1-(furan-2-yl)-3-phenylbutan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4,4-trifluoro-1-(furan-2-yl)-3-phenylbutan-1-one(1499198-35-4)
• EPA Substance Registry System: 4,4,4-trifluoro-1-(furan-2-yl)-3-phenylbutan-1-one(1499198-35-4)

Safety Data

• Hazardous Substances Data: 1499198-35-4(Hazardous Substances Data)

Upstream product

• 434-45-7 2,2,2-Trifluoroacetophenone 
• 15109-97-4 2-(2-furyl)-2-oxoethyl(triphenyl)phosphonium bromide 
• 3988-74-7 1-(2-furyl)-3-phenylpropen-1-one 
• 147531-11-1 trifluoromethanesulfonic acid diphenyl(trifluoromethyl)sulfonium salt 

Relevant articles and documents

Benzylamine as Hydrogen Transfer Agent: Cobalt-Catalyzed Chemoselective C=C Bond Reduction of β-Trifluoromethylated α,β-Unsaturated Ketones via 1,5-Hydrogen Transfer

An efficient cobalt-catalyzed chemoselective reduction of β-CF3-α,β-unsaturated ketones using benzylamine as hydrogen transfer agent involving intramolecular 1,5-hydrogen transfer is reported. The reaction proceeded smoothly with a relatively w

Regioselective 1,4-trifluoromethylation of α,β-unsaturated ketones via a S-(trifluoromethyl)diphenylsulfonium salts/copper system

Regioselective conjugate 1,4-trifluoromethylation of α,β- unsaturated ketones by the use of shelf-stable electrophilic trifluoromethylating reagents, S-(trifluoromethyl)diphenylsulfonium salts and copper under mild conditions is described. A wide range of acyclic aryl-aryl-enones and aryl-alkyl-enones were converted into β- trifluoromethylated ketones in low to moderate yields.