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| Product | Description | |
|---|---|---|
| Trimethylsulfonium Iodide | Treatment with strong base yields the dimethylsulfonium methylide which reacts in-situ with the carbonyl group of ketones to form epoxides or allylic alcohols. Group: Battery materials dye-sensitized solar cell (dssc) materials. Alternative Names: S111 I. CAS No. 2181-42-2. Product ID: trimethylsulfanium; iodide. Molecular formula: 204.07. Mole weight: C3H9IS. C[S+](C)C.[I-]. InChI=1S/C3H9S.HI/c1-4(2)3; /h1-3H3; 1H/q+1; /p-1. VFJYIHQDILEQNR-UHFFFAOYSA-M. >98.0%T. |  |
| Trimethylsulfonium Iodide | Treatment with strong base yields the dimethylsulfonium methylide which reacts in-situ with the carbonyl group of ketones to form epoxides or allylic alcohols. Group: Heterocyclic organic compound. Alternative Names: S111 I. CAS No. 2181-42-2. Molecular formula: C3H9IS. Mole weight: 204.07. Appearance: White to Almost white powder to crystal. Purity: >98.0%T. IUPACName: trimethylsulfanium;iodide. Canonical SMILES: C[S+](C)C.[I-]. ECNumber: 218-555-4. Catalog: ACM2181422. |  |
| Trimethylsulfonium Iodide | Trimethylsulfonium iodide is a salt that is usually dissolved in strong base in order to synthesize epoxides in-situ. Trimethylsulfonium iodide also has the potential to inhibit human placental diamine oxidase. Group: Biochemicals. Grades: Highly Purified. CAS No. 2181-42-2. Pack Sizes: 1g, 10g. Molecular Formula: C3H9IS, Molecular Weight: 204.07. US Biological Life Sciences. |  Worldwide |
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