| Weight | 218.074 g/mol |
|---|---|
| Formula | C2F6O3S |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
trifluoromethyl trifluoromethanesulfonate (3582-05-6)
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- Preparation and Properties of Bis(trifluoromethylsulfuryl) Peroxide and Trifluoromethyl Trifluoromethanesulfonate (Inorganic Chemistry, 1965)
- Trifluoromethyl trifluoromethanesulfonate (CF3SO2OCF3) (Tetrahedron Letters, 1979)
- Gas-phase structure and vibrational properties of trifluoromethyl trifluoromethanesulfonate, CF3SO2OCF3 (European Journal of Inorganic Chemistry, 2007)
- The Simple Practical Preparation of Trifluoromethyl Trifluoromethanesulfonate (Triflate)1 (Synthesis, 1976)
- Solvolysis of 2-(trifluoromethyl)-2-propyl trifluoromethanesulfonate. Solvent, salt, and. beta. -deuterium isotope effects. Substituents effect of a strongly deactivating group and rate-limiting solvent-assisted elimination (Journal of the American Chemical Society, 1981)
- Nucleosides. 137. (Trifluoromethyl)sulfonyl (triflyl) migration. Synthesis of 6,3'-anhydro-3-benzyl-1-(5-chloro-5-deoxy-.beta.-D-xylofuranosyl)barbituric acid from the 2'-trifluoromethanesulfonate (triflate) of 6,5'-anhydro-3-benzyl-1-.beta.-D-ribofuranosylbarbituric acid (Journal of Organic Chemistry, 1986)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(OS(=O)(=O)C(F)(F)F)(F)(F)F
-
InChIKeyGVZFDPPAJXHNGL-UHFFFAOYSA-N
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trifluoromethyl trifluoromethanesulfonate
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