| Weight | 220.075 g/mol |
|---|---|
| Formula | C3H9IOS |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Trimethylsulfoxonium iodide (1774-47-6)
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- Microwave-Assisted Efficient Methylation of Alkyl and Arenesulfonamides with Trimethylsulfoxonium Iodide and KOH (Synthetic Communications, 2008)
- Carbon-13 chemical-shift tensors and relaxation phenomena in solid trimethylsulfoxonium iodide. A single-crystal NMR study (Journal of Magnetic Resonance, Series A, 1995)
- [Studies on phenoxazine related compounds. IV. Reaction of imidazo (4,5,1-kl)phenoxazine and trimethylsulfoxonium iodide]. (Yakugaku Zasshi-journal of The Pharmaceutical Society of Japan, 1970)
- ChemInform Abstract: Reaction of Diaryltellurium Oxides with Trimethylsulfoxonium Iodide. (ChemInform, 1987)
- Reaction of diaryltelluroxides with trimethylsulfoxonium iodide (1987)
- ChemInform Abstract: Microwave-Assisted Efficient Methylation of Alkyl and Arenesulfonamides with Trimethylsulfoxonium Iodide and KOH. (ChemInform, 2009)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC[S+](=O)(C)C.[I-]
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InChIKeyBPLKQGGAXWRFOE-UHFFFAOYSA-M
- Pubchem - Trimethylsulfoxonium iodide
- Wikipedia - Trimethylsulfoxonium iodide
Trimethylsulfoxonium iodide is a sulfoxonium salt. It is used to generate dimethyloxosulfonium methylide by reaction with sodium hydride. The latter compound is used as a methylene-transfer reagent, and is used to prepare epoxides.
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