| Weight | 96.582 g/mol |
|---|---|
| Formula | C2H5ClS |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
Chloromethyl methyl sulfide (2373-51-5)
chlorodimethyl sulfide
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- Intramolecular cyclization via onium salts: a novel synthesis of 1,3-thiazolidines from chloromethyl (trimethylsilyl)methyl sulfide and nitrogen-containing heteroaromatic compounds (Journal of Organic Chemistry, 1987)
- Conformational and stereoelectronic investigation of chloromethyl methyl sulfide and its sulfinyl and sulfonyl analogs (Journal of Molecular Structure, 2006)
- Superelectrophilic methylthiomethylation of aromatics with chloromethyl methyl sulfide/aluminum chloride (MeSCH2Cl:2 AlCl3) reagent (Synthesis, 1994)
- Addition reaction of chloromethyl methyl sulfide to olefins in sulfuric acid. Synthesis of 3-(methylthio)propionaldehyde (Journal of Organic Chemistry, 1970)
- Raman and infrared spectra, conformational stability, and ab initio calculations for chloromethyl methyl sulfide (Journal of Raman Spectroscopy, 2000)
- HCl Elimination from Ethanesulfenyl Chloride (I) and Chlorodimethyl Sulfide (ChemInform, 1992)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - chlorodimethyl sulfide
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SMILESCSCCl
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InChIKeyJWMLCCRPDOIBAV-UHFFFAOYSA-N
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