41463-86-9

Basic information

• Product Name: 4,4,4-TRIFLUORO-3-HYDROXY-1-PHENYL-BUT-2-EN-1-ONE
• Synonyms: Benzoyltrifluoroacetoneenol
• CAS NO: 41463-86-9
• Molecular Formula: C₁₀H₇F₃O₂
• Molecular Weight: 0
• Mol File: 41463-86-9.mol
• Article Data: 13

Chemical Properties

• Boiling Point: 211.71°C (rough estimate)
• Appearance: /
• CAS DataBase Reference: 4,4,4-TRIFLUORO-3-HYDROXY-1-PHENYL-BUT-2-EN-1-ONE(CAS DataBase Reference)
• NIST Chemistry Reference: 4,4,4-TRIFLUORO-3-HYDROXY-1-PHENYL-BUT-2-EN-1-ONE(41463-86-9)
• EPA Substance Registry System: 4,4,4-TRIFLUORO-3-HYDROXY-1-PHENYL-BUT-2-EN-1-ONE(41463-86-9)

Safety Data

• Hazardous Substances Data: 41463-86-9(Hazardous Substances Data)

Upstream product

• 383-63-1 ethyl trifluoroacetate, 
• 98-86-2 acetophenone 

Downstream Products

• 80460-22-6 (Z)-4,4,4-Trifluoro-3-methylamino-1-phenyl-but-2-en-1-one 
• 80460-23-7 (Z)-1,1,1-Trifluoro-4-methylamino-4-phenyl-but-3-en-2-one 
• 1291099-87-0 1-methyl-4-nitroso-5-phenyl-3-(trifluoromethyl)-1H-pyrazole 
• 1414573-15-1 1-methyl-5-phenyl-3-(trifluoromethyl)-1H-pyrazol-4-amine 
• 842141-03-1 5-phenyl-3-(trifluoromethyl)-1H-pyrazol-4-amine 
• 824969-35-9 4-nitroso-5-phenyl-3-(trifluoromethyl)-1H-pyrazole 

Relevant articles and documents

Nickel-Catalyzed Aminofluoroalkylation of Alkenes: Access to Difluoroalkylated N-Containing Heterocyclic Compounds

A nickel-catalyzed aminofluoroalkylative cyclization of unactive alkenes with iododifluoromethyl ketones was developed to construct versatile difluoroalkylated Nitrogen-containing heterocycles including aziridines, pyrrolidines and piperidines in moderate to high yields. This method features a broad substrate scope and has been demonstrated on gram scale.

Preparation method of gamma-bromine-beta, gamma-alkenyl fluoroketone derivatives

The invention relates to a preparation method of gamma-bromine-beta, gamma-alkenyl fluoroketone derivatives, which comprises the following steps: dissolving a compound represented by formula (IV) andcorresponding alkyne in acetone, adding bis (triphenylph

Nickel-Catalyzed Coupling Reaction of α-Bromo-α-fluoroketones with Arylboronic Acids toward the Synthesis of α-Fluoroketones

A nickel-catalyzed coupling reaction of α-bromo-α-fluoroketones with arylboronic acids was reported, which provides an efficient pathway to access 2-fluoro-1,2-diarylethanones in high yields. We also disclosed the synthesis of the monofluorination agents