125440-38-2

Basic information

• Product Name: 1,2-difluoro-1,1,2-triphenylethane
• Synonyms: 1,2-difluoro-1,1,2-triphenylethane
• CAS NO: 125440-38-2
• Molecular Weight: 294.344
• Mol File: 125440-38-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 1,2-difluoro-1,1,2-triphenylethane(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-difluoro-1,1,2-triphenylethane(125440-38-2)
• EPA Substance Registry System: 1,2-difluoro-1,1,2-triphenylethane(125440-38-2)

Safety Data

• Hazardous Substances Data: 125440-38-2(Hazardous Substances Data)

Upstream product

• 58-72-0 Triphenylethylene 
• 632-51-9 1,1,2,2-tetraphenylethylene 

Relevant articles and documents

Rearrangement of phenylethenes on reaction with iodine-xenon difluoride

(matrix presented) Phenyl-substituted ethenes react with iodine and xenon difluoride to provide difluorinated products. Iodofluoro intermediates react with xenon difluoride to produce transient iodine difluoride species that lose IF and F- and produce carbocations.

N-Fluorobisimides: Reactions with Some Olefins via α-Fluoro Carbocationic Intermediates

N-Fluorobisimides are a new class of electrophilic fluorinating agents.Reaction of (CF3SO2)2NF (1) with olefins gave various products, depending on the reaction conditions and the structure of the substrate.In solvents of higher nucleophilicity such as H2O, acetic acid, aqueous HCl, and (HF)nPy, α-fluorohydrins and their acetates, α,β-chlorofluoro- and α,β-difluoroalkanes were obtained.In acetic acid, trans-stilbene and tetraphenylethylene produced the rearranged, nonfluorinated aldehyde and ketone.Evidence is presented for the reactions proceeding via a one-electron transfer mechanism involving α-fluorocarbocationic intermediates.