947-24-0

Basic information

• Product Name: Benzene, [2-[(trifluoromethyl)sulfonyl]ethenyl]-, (E)-
• Synonyms: (E)-1-Phenyl-2-(trifluoromethylsulphonyl)ethene;((E)-2-Trifluoromethanesulfonyl-vinyl)-benzene
• CAS NO: 947-24-0
• Molecular Formula: C9H7F3O2S
• Molecular Weight: 236.21100
• Mol File: 947-24-0.mol

Chemical Properties

• Melting Point: 52 - 53 °C
• Boiling Point: 312.0±42.0 °C(Predicted)
• Density: 1.407±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Benzene, [2-[(trifluoromethyl)sulfonyl]ethenyl]-, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, [2-[(trifluoromethyl)sulfonyl]ethenyl]-, (E)-(947-24-0)
• EPA Substance Registry System: Benzene, [2-[(trifluoromethyl)sulfonyl]ethenyl]-, (E)-(947-24-0)

Safety Data

• Hazardous Substances Data: 947-24-0(Hazardous Substances Data)

Upstream product

• 100-42-5 styrene 
• 421-83-0 trifluoromethane sulfonyl chloride 
• 4206-67-1 iodo(trimethylsilyl)methane 
• 358-23-6 trifluoromethylsulfonic anhydride 
• 100-52-7 benzaldehyde 
• 158530-84-8 Trifluoromethanesulfonylmethyl-phosphonic acid dimethyl ester 
• 756-79-6 dimethyl methane phosphonate 

Downstream Products

• 18138-77-7 (E)-2-styryltetrahydrofuran 
• 18869-27-7 (E)-(2-cyclohexylvinyl)benzene 

Relevant articles and documents

Cu Photoredox Catalysts Supported by a 4,6-Disubstituted 2,2′-Bipyridine Ligand: Application in Chlorotrifluoromethylation of Alkenes

Interest in base metal catalysis motivates the development of Cu-based photoredox catalysts for organic synthesis. However, only a few Cu catalysts have been applied in photoredox reactions, the majority of which contain one or two 1,10-phenanthroline lig

A mild and convenient synthesis of functionalized methyl triflones and vinyl triflones

A general route for the synthesis of methyl triflone derivatives utilizing triflic anhydride is described. Stereoselective synthesis of E-vinyl and dienyl triflones has been accomplished by the Peterson olefination reaction of α-silyl triflone anions.

Novel Perfluoroalkylation of Alkenes with Perfluoroalkanesulphonyl Chlorides Catalysed by a Ruthenium(II) Complex

The perfluoroalkylation of acyclic and cyclic alkenes by perfluoroalkanesulphonyl chlorides 1 has been investigated in the presence of a ruthenium(II) catalyst.The addition reactions proceeded smoothly, with extrusion of sulphur dioxide, in alkenes posses