197566-47-5

Basic information

• Product Name: (E)-4,4,4-trifluoro-3-methyl-1-phenyl-2-buten-1-ol
• Synonyms: (E)-4,4,4-trifluoro-3-methyl-1-phenyl-2-buten-1-ol
• CAS NO: 197566-47-5
• Molecular Weight: 216.203
• Mol File: 197566-47-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (E)-4,4,4-trifluoro-3-methyl-1-phenyl-2-buten-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-4,4,4-trifluoro-3-methyl-1-phenyl-2-buten-1-ol(197566-47-5)
• EPA Substance Registry System: (E)-4,4,4-trifluoro-3-methyl-1-phenyl-2-buten-1-ol(197566-47-5)

Safety Data

• Hazardous Substances Data: 197566-47-5(Hazardous Substances Data)

Upstream product

• 851645-72-2 (E)-4,4,4-trifluoro-3-methyl-1-phenyl-2-buten-1-one 
• 6048-29-9 triphenylphenacylphosphonium bromide 

Downstream Products

• 106352-39-0 4,4,4-trifluoro-3-methyl-1-phenylbutan-1-one 

Relevant articles and documents

Synthesis of trifluoro- or difluoromethylated olefins by regio- and stereocontrolled SN2′ reactions of gem-difluorinated vinyloxiranes

This paper presents a highly stereoselective synthesis of trifluoro- or difluoromethylated olefins via an SN2′ type fluorination or reductions of gem-difluorinated vinyloxiranes. Their fluorination with HF-Py furnished trifluoromethylated allyl

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