| Weight | 168.523 g/mol |
|---|---|
| Formula | CClF3O2S |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Trifluoromethanesulfonyl chloride (421-83-0)
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- Trifluoromethanesulfonyl chloride, a mild chlorinating agent (Tetrahedron Letters, 1979)
- Trifluoromethanesulfonyl chloride for identification of oxygen, nitrogen, and sulfur functional groups by fluorine-19 nuclear magnetic resonance spectrometry (Analytical Chemistry, 1982)
- Importance of poly(ethylene oxide)-modification and chloride anion for the electron transfer reaction of cytochrome c in 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide (Electrochimica Acta, 2006)
- Synthetic Methods and Reactions; 721. Mild Fragmentative C-C Bond Cleavage of -Hydroxyketoximes with Trifluoromethanesulfonic Anhydride, Trifluoroacetic Anhydride, or Trifluoromethanesulfonyl Chloride. (Synthesis, 1980)
- Transition metal-free direct trifluoromethylthiolation of indoles using trifluoromethanesulfonyl chloride in the presence of triphenylphosphine. (Organic and Biomolecular Chemistry, 2017)
- Cathodic chloride extraction treatment of a late bronze-age artifact affected by bronze disease in room-temperature ionic-liquid 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide (EMI-TFSI) (Journal of Solid State Electrochemistry, 2010)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(F)(F)(F)S(=O)(=O)Cl
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InChIKeyGRGCWBWNLSTIEN-UHFFFAOYSA-N
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