Weight | 178.131 g/mol |
---|---|
Formula | C3H5F3O3S |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 2 |
Ethyl trifluoromethanesulfonate (425-75-2)
Score:
#108 in Physical chemistry
,
#2377 in Physics
,
#7261 in Chemistry
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- Electropolymerization of pyrrole in 1-ethyl-3-methylimidazolium trifluoromethanesulfonate room temperature ionic liquid (Electrochemistry Communications, 2002)
- Physical and electrochemical properties of ionic liquids 1-ethyl-3-methylimidazolium tetrafluoroborate, 1-butyl-3-methylimidazolium trifluoromethanesulfonate and 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl)imide (Journal of Molecular Liquids, 2010)
- Volumetric and Ultrasonic Studies of 1-Ethyl-3-methylimidazolium Trifluoromethanesulfonate Ionic Liquid with Methanol, Ethanol, 1-Propanol, and Water at Several Temperatures (Journal of Chemical & Engineering Data, 2007)
- Electrooxidative polymerization of aromatic compounds in 1-ethyl-3-methylimidazolium trifluoromethanesulfonate room-temperature ionic liquid (Journal of Electroanalytical Chemistry, 2003)
- Ionic liquids as entrainers in extractive distillation : Isobaric vapor-liquid equilibria for acetone + methanol + 1 -ethyl -3 -methylimidazolium trifluoromethanesulfonate (Journal of Chemical & Engineering Data, 2007)
- tert-Amyl Ethyl Ether Separation from Its Mixtures with Ethanol Using the 1-Butyl-3-methylimidazolium Trifluoromethanesulfonate Ionic Liquid: Liquid-Liquid Equilibrium (Industrial & Engineering Chemistry Research, 2004)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCOS(=O)(=O)C(F)(F)F
-
InChIKeyUVECLJDRPFNRRQ-UHFFFAOYSA-N
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Similar Compounds
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trifluoromethyl trifluoromethanesulfonate
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Copper(II) trifluoromethanesulfonate
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trifluoromethane(2h)sulfonic acid
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53555-41-2
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Phenyl trifluoromethanesulfonate
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29540-84-9
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697-18-7
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69739-34-0
(69739-34-0)
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1-Naphthyl trifluoromethanesulfonate
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Acetic acid, difluorosulfo-
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85272-31-7
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126613-06-7
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bis(2,2,2-trifluoroethyl) sulfite
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36457-58-6
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