
CAS 185739-14-4
:Fórmula:C9H8F2O3S
InChI:InChI=1S/C9H8F2O3S/c1-7-2-4-8(5-3-7)15(12,13)14-6-9(10)11/h2-6H,1H3
Clave InChI:ZQLLPWMNXQYESO-UHFFFAOYSA-N
SMILES:CC1=CC=C(C=C1)S(=O)(=O)OC=C(F)F
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2,2-Difluoroethenyl 4-Methylbenzene-1-sulfonate
CAS:Fórmula:C9H8F2O3SPureza:>98.0%(GC)Forma y color:Colorless to Light yellow clear liquidPeso molecular:234.222,2-Difluorovinyl 4-methylbenzenesulfonate
CAS:2,2-Difluorovinyl 4-methylbenzenesulfonateFórmula:C9H8F2O3SPureza:95%Forma y color:LiquidPeso molecular:234.222,2-Difluoroethenyl-4-methylbenzenesulfonate
CAS:Fórmula:C9H8F2O3SPureza:97%Forma y color:LiquidPeso molecular:234.21982,2-Difluoroethenyl 4-methylbenzene-1-sulfonate
CAS:2,2-Difluoroethenyl 4-methylbenzene-1-sulfonateFórmula:C9H8F2O3SPureza:95%Peso molecular:234.222,2-Difluorovinyl 4-methylbenzenesulfonate
CAS:Pureza:95%Forma y color:LiquidPeso molecular:234.22000122,2-Difluoroethenyl 4-methylbenzene-1-sulfonate
CAS:2,2-Difluoroethenyl 4-methylbenzene-1-sulfonate is a coupling reagent that is used to form terminal alkynes. It reacts with fluorescing compounds to yield 2,2-difluoroethenyl esters or thioesters and can be used as a source of terminal alkynes. This reagent has been shown to react with various aromatic compounds in the presence of base. The reaction results in the formation of a difluorinated aromatic compound and a sulfonic acid salt.
Fórmula:C9H8F2O3SPureza:Min. 95%Peso molecular:234.22 g/mol





