| Weight | 134.2 g/mol |
|---|---|
| Formula | C5H10O2S |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 3 |
Ethyl (methylthio)acetate (4455-13-4)
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- A NOVEL CYCLIZATION OF ELECTRON DEFICIENT N-BENZENE-SULFONYL-BETA -PHENETHYLAMINES USING ETHYL CHLORO-(METHYLTHIO)ACETATE. SYNTHESIS OF ETHYL 1,2,3,4- TETRA-HYDROISOQUINOLINE-1-CARBOXYLATES (Heterocycles, 1996)
- Synthesis of Ethyl Arylacetates by Means of Friedel-Crafts Reaction of Aromatic Compounds with Ethyl -Chloro--(methylthio) acetate (Chemical & Pharmaceutical Bulletin, 1982)
- ChemInform Abstract: SYNTHESIS OF ETHYL ARYLACETATES BY MEANS OF FRIEDEL-CRAFTS REACTION OF AROMATIC COMPOUNDS WITH ETHYL -CHLORO--(METHYLTHIO)ACETATE (ChemInform, 1982)
- Ethyl (Methylthio)acetate (2001)
- ChemInform Abstract: A Novel Cyclization of Electron-Deficient N-Benzenesulfonyl-- phenethylamines Using Ethyl Chloro(methylthio)acetate. Synthesis of Ethyl 1,2,3,4-Tetrahydroisoquinoline-1-carboxylates. (ChemInform, 2010)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCOC(=O)CSC
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InChIKeyMDIAKIHKBBNYHF-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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Ethyl (methylthio)acetate
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