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235789-75-0

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235789-75-0 Structure

235789-75-0 Structure
IdentificationBack Directory
[Name]

EMI-FSI 1-Ethyl-3-methylimidazolium Bis(fluorosulfonyl) imide
[CAS]

235789-75-0
[Synonyms]

EMIFSI
IL 110
Elexcel AS 110
Elexcel IL 110
EMIm bis(fluorosulfonyl)amide
Methylethylimidazolium bis(fluorosulfonyl)imide
1-Ethyl-3-methylimidazolium Bis(fluorosulfonyl) imide
EMI-FSI 1-Ethyl-3-methylimidazolium Bis(fluorosulfonyl) imide
[Molecular Formula]

C6H11F2N3O4S2
[MDL Number]

MFCD17018943
[MOL File]

235789-75-0.mol
[Molecular Weight]

291.296
Chemical PropertiesBack Directory
[Melting point ]

-18 °C
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H335-H319-H315
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362
Hazard InformationBack Directory
[Description]

1-Ethyl-3-methylimidazolium bis(fluorosulfonyl)imide is a chemical that has been used in organic solvents to increase the rate of reaction. It is an organic compound with a sulfonyl group, which is a functional group consisting of a sulfonate ester and a sulfonic acid.
[Uses]

1-Ethyl-3-methylimidazolium bis(fluorosulfonyl)imide binds to hydrogen and forms hydrogen bonds with other molecules, which increases viscosity and intramolecular interaction energies. This compound also interacts with other compounds through van der Waals interactions and covid-19 pandemic interactions. It can be synthesized by reacting methylamine with 2-chloroethanesulfonylfluoride in the presence of ammonium chloride.
Spectrum DetailBack Directory
[Spectrum Detail]

1-Ethyl-3-methylimidazolium bis(fluorosulfonyl)imide(235789-75-0)1HNMR
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