| Weight | 226.175 g/mol |
|---|---|
| Formula | C7H5F3O3S |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
Phenyl trifluoromethanesulfonate (17763-67-6)
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- Efficient synthesis of 2-(trimethylsilyl)phenyl trifluoromethanesulfonate: a versatile precursor to o-benzyne. (Journal of Organic Chemistry, 2009)
- Tandem thia-Fries rearrangement--cyclisation of 2-(trimethylsilyl)phenyl trifluoromethanesulfonate benzyne precursors. (Chemical Communications, 2013)
- Formation of Phenyl Cations in the Sovolysis of a Dienynyl Trifluoromethanesulfonate (Angewandte Chemie, 1979)
- Synthesis and nucleophilic dealkylation of poly[alkyl-(4-(phenylthio)phenyl)sulfonium trifluoromethanesulfonate]s (Macromolecules, 1998)
- 2-Phenyl-1,3-benzodithiolylium trifluoromethanesulfonate : a reagent for the conversion of alcohols into benzyl ethers and benzoates under mild conditions (Tetrahedron Letters, 1990)
- Isomer Dependence in the Assembly and Lability of Silver(I) Trifluoromethanesulfonate Complexes of the Heteroditopic Ligands, 2-, 3-, and 4-[Di(1H-pyrazolyl)methyl]phenyl(di-p-tolyl)phosphine (Inorganic Chemistry, 2014)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)OS(=O)(=O)C(F)(F)F
-
InChIKeyGRJHONXDTNBDTC-UHFFFAOYSA-N
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Phenyl trifluoromethanesulfonate
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