55009-95-5

Basic information

• Product Name: 1.1.1.2.2-Pentafluor-4-phenylbut-3-en
• CAS NO: 55009-95-5
• Molecular Weight: 222.158
• Mol File: 55009-95-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1.1.1.2.2-Pentafluor-4-phenylbut-3-en(CAS DataBase Reference)
• NIST Chemistry Reference: 1.1.1.2.2-Pentafluor-4-phenylbut-3-en(55009-95-5)
• EPA Substance Registry System: 1.1.1.2.2-Pentafluor-4-phenylbut-3-en(55009-95-5)

Safety Data

• Hazardous Substances Data: 55009-95-5(Hazardous Substances Data)

Upstream product

• 354-64-3 Pentafluoroethyl iodide 
• 103-64-0 bromostyrene 
• 559-91-1 1-phenylperfluorobutan-1-one 
• 81290-20-2 (trifluoromethyl)trimethylsilane 
• 120120-26-5 (trifluoromethyl)triethylsilane 
• 2923-18-4 sodium 2,2,2-trifluoroacetate 

Downstream Products

• 55009-90-0 (pentafluorobut-1-yn-1-yl)benzene 

Relevant articles and documents

Efficient trifluoromethylation of activated and non-activated alkenyl halides by using (trifluoromethyl)trimethylsilane

An efficient method for the trifluoromethylation of halogenated double bonds by using in situ generated "trifluoromethyl copper" is described. Herein, the most common trifluoromethyl source, (trifluoromethyl) trimethylsilane, was converted selectively int

Sodium Perfluoroalkane Carboxylates as Sources of Perfluoroalkyl Groups

Sodium trifluoroacetate, in the presence of copper(I) iodide, is used as a source of trifluoromethyl to replace halogen by trifluoromethyl in benzenoid and heterocyclic aromatic systems, as well as in alkenyl and alkyl halogen compounds.The mechanism of this interesting copper-assisted process has been explored and an intermediate of the form - is proposed.Introduction of higher perfluoroalkyl groups from their respective sodium perfluoroalkane carboxylates has been demonstrated and the machanistic features are compared with those of the trifluoromethylation process.