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ChemicalBook--->CAS DataBase List--->677-25-8

677-25-8

677-25-8 Structure

677-25-8 Structure
IdentificationBack Directory
[Name]

ethylenesulphonyl fluoride
[CAS]

677-25-8
[Synonyms]

Fluorosulfonylethene
Ethenesulfonylfluoride
Vinyl sulfonyl fluoride
ethylenesulphonyl fluoride
Ethenesulfonyl fluoride,97%
Ethenesulfonic acid fluoride
[EINECS(EC#)]

211-640-7
[Molecular Formula]

C2H3FO2S
[MDL Number]

MFCD00051388
[MOL File]

677-25-8.mol
[Molecular Weight]

110.11
Chemical PropertiesBack Directory
[Boiling point ]

44-46 °C(Press: 50 Torr)
[density ]

1.328 g/mL at 25 °C
[refractive index ]

n20/D1.385
[Fp ]

40℃
[form ]

liquid
[EPA Substance Registry System]

Ethenesulfonyl fluoride (677-25-8)
Safety DataBack Directory
[Symbol(GHS) ]


GHS02,GHS05,GHS06,GHS08
[Signal word ]

Danger
[Hazard statements ]

H226-H301+H311+H331-H314-H335-H341
[Precautionary statements ]

P202-P210-P280-P303+P361+P353-P304+P340+P310-P305+P351+P338
[Hazard Codes ]

T,C
[Risk Statements ]

23/24/25-34-68
[Safety Statements ]

26-36/37/39-45
[RIDADR ]

UN 2920 3(8) / PGII
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

Ethenesulfonyl fluoride can be used as a reactant to synthesize:
  • β-Arylethenesulfonyl fluorides via palladium(II) acetate-catalyzed Heck-Matsuda reaction with arenediazonium tetrafluoroborates.
  • Bisalkylsulfonyl fluoride(BSF) monomers via Michael addition reaction with amines/anilines. BSF monomers are applicable in the synthesis of polysulfonates.
  • Cyclobutane-fused pyridinyl sulfonyl fluorides by photocatalytic [2 + 2] cycloaddition with pyridones or isoquinolones.
[reaction suitability]

reaction type: click chemistry
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