1340343-75-0

Basic information

• Product Name: 4,4,4-trifluoro-1-(2-methoxyphenyl)butan-1-one
• Synonyms: 4,4,4-trifluoro-1-(2-methoxyphenyl)butan-1-one
• CAS NO: 1340343-75-0
• Molecular Weight: 232.202
• Mol File: 1340343-75-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 4,4,4-trifluoro-1-(2-methoxyphenyl)butan-1-one(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4,4-trifluoro-1-(2-methoxyphenyl)butan-1-one(1340343-75-0)
• EPA Substance Registry System: 4,4,4-trifluoro-1-(2-methoxyphenyl)butan-1-one(1340343-75-0)

Safety Data

• Hazardous Substances Data: 1340343-75-0(Hazardous Substances Data)

Upstream product

• 887144-94-7 Togni's reagent II 
• 58824-49-0 1-(2-methoxyphenyl)prop-2-en-1-ol 
• 353-83-3 1,1,1-trifluoro-2-iodoethane 
• 612-15-7 o-methoxystyrene 
• 606-45-1 2-methoxybenzoic acid methyl ester 
• 692-51-3 (E)-trimethyl(3,3,3-trifluoroprop-1-en-1-yl)silane 
• 135-02-4 ortho-anisaldehyde 

Relevant articles and documents

A Concise Copper-Catalyzed Oxytrifluoromethylation of Allyl Alcohols

An efficient oxytrifluoromethylation of 1-aryl-substituted allyl alcohols has been developed using Togni's reagent II as a trifluoromethylation reagent and copper(I) chloride as a catalyst. This reaction proceeded through a one-pot process of trifluoromet

Copper-catalysed ring-opening trifluoromethylation of cyclopropanols

A copper-catalysed ring-opening trifluoromethylation reaction of cyclopropanols has been developed. Various β-trifluoromethyl ketones are obtained in good to excellent yields under mild reaction conditions. The present method also exhibits good functional-group compatibility. The mechanism of this new ring-opening trifluoromethylation reaction was investigated by radical trapping reactions.