58174-56-4

Upstream product

• 811-97-2 1,1,1,2-tetrafluoroethane 
• 625-99-0 3-iodochlorobenzene 
• 40193-72-4 α,β-dibromo-α,β,β-trifluorostyrene 
• 447-14-3 1,2,2-trifluorostyrene 
• 309-13-7 1-chloro-3-(pentafluoroethyl)benzene 
• 946152-81-4 1-(3'-chlorophenyl)-1-trimethylsilyl-1,2,2,2-tetrafluoroethane 

Relevant academic research and scientific papers

Fluoride ion-catalyzed 1,2-desilylative defluorination: Syntheses of 1-substituted 2,2-difluorostyrenes

(Chemical Equation Presented) 1-(3′-Chlorophenyl)-1-trimethylsilyl-1, 2,2,2-tetrafluoroethane has been prepared in an excellent yield by the Mg-promoted defluorinative silylation of 3-chloropentafluoroethylbenzene and transformed to a series of 1-substitu

Room temperature preparation of trifluoroethenylzinc reagent by metalation of the readily available halocarbon HFC-134a and an efficient, economically viable synthesis of 1,2,2-trifluorostyrenes

Trifluoroethenylzinc reagent [CF2=CFZnX] was generated from the readily available halocarbon HFC-134a by an in situ metalation-transmetalation procedure at temperatures near to room temperature (15-20 °C). By systematic standardization of the m