106352-39-0

Basic information

• Product Name: 4,4,4-trifluoro-3-methyl-1-phenylbutan-1-one
• Synonyms: 4,4,4-trifluoro-3-methyl-1-phenylbutan-1-one
• CAS NO: 106352-39-0
• Molecular Weight: 216.203
• Mol File: 106352-39-0.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 4,4,4-trifluoro-3-methyl-1-phenylbutan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4,4-trifluoro-3-methyl-1-phenylbutan-1-one(106352-39-0)
• EPA Substance Registry System: 4,4,4-trifluoro-3-methyl-1-phenylbutan-1-one(106352-39-0)

Safety Data

• Hazardous Substances Data: 106352-39-0(Hazardous Substances Data)

Upstream product

• 1771-65-9 2-methyl-4-oxo-4-phenylbutanoic acid 
• 1680206-12-5 Grushin’s reagent 
• 495-41-0 1-phenylbut-2-en-1-one 
• 147531-11-1 trifluoromethanesulfonic acid diphenyl(trifluoromethyl)sulfonium salt 
• 197566-47-5 (E)-4,4,4-trifluoro-3-methyl-1-phenyl-2-buten-1-ol 
• 6048-29-9 triphenylphenacylphosphonium bromide 
• 851645-72-2 (E)-4,4,4-trifluoro-3-methyl-1-phenyl-2-buten-1-one 

Downstream Products

• 106352-41-4 (2R,3S)-4,4,4-Trifluoro-2-hydroxy-3-methyl-1-phenyl-butan-1-one 
• 106352-41-4 (2S,3S)-4,4,4-Trifluoro-2-hydroxy-3-methyl-1-phenyl-butan-1-one 

Relevant articles and documents

Silver-Catalyzed Decarboxylative Trifluoromethylation of Aliphatic Carboxylic Acids

The silver-catalyzed decarboxylative trifluoromethylation of aliphatic carboxylic acids is described. With AgNO3 as the catalyst and K2S2O8 as the oxidant, the reactions of aliphatic carboxylic acids with (bpy)C

Synthesis of β-CF3 ketones from trifluoromethylated allylic alcohols by ruthenium catalyzed isomerization

This work describes the optimization process for the synthesis of β-trifluoromethylated ketones from trifluoromethylated allylic alcohols. This transformation proceeds through a ruthenium catalyzed isomerization under mild conditions with high atom econom

Ruthenium-catalyzed redox isomerization of trifluoromethylated allylic alcohols: Mechanistic evidence for an enantiospecific pathway

Transfer news: A synthetic approach to chiral β-CF3- substituted saturated carbonyl compounds has been developed in which ruthenium complexes efficiently catalyze the redox isomerization of CF3-bearing allylic alcohols by an intramol