| Weight | 106.146 g/mol |
|---|---|
| Formula | C3H6O2S |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
METHYL THIOGLYCOLATE (2365-48-2)
methyl thioglycolate, sodium salt · methyl mercaptoacetate · thioglycolic acid methyl ester
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- Proposed Structure of the Neocarzinostatin Chromophore-Methyl Thioglycolate Adduct; A Mechanism for the Nucleophilic Activation of Neocarzinostatin (Tetrahedron Letters, 1987)
- Stereochemical assignment of neocarzinostatin chromophore. Structures of neocarzinostatin chromophore-methyl thioglycolate adducts (Journal of the American Chemical Society, 1988)
- Reductive and nucleophilic activation products of dynemicin A with methyl thioglycolate. A rational mechanism for DNA cleavage of the thiol-activated dynemicin A (Biochemistry, 1991)
- Addition of Methyl Thioglycolate and Benzylamine to (Z)-Ligustilide, a Bioactive Unsaturated Lactone Constituent of Several Herbal Medicines. An Improved Synthesis of (Z)-Ligustilide (Journal of Natural Products, 1995)
- Reversed-phase ion-pair high-performance liquid chromatography of mercaptoacetate and N-acetylcysteine after derivatization with N-(1-pyrene)maleimide and N-(7-dimethylamino-4-methyl-3-coumarinyl)maleimide (Journal of Chromatography B: Biomedical Sciences and Applications, 1982)
- The Preparation of 4-Thiazolidones. III. The Reaction of Methyl Thioglycolate with Benzylidene Dialkylaminoalkylamines (Journal of the American Chemical Society, 1949)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - methyl thioglycolate, sodium salt
- methyl mercaptoacetate
- thioglycolic acid methyl ester
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SMILESCOC(=O)CS
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InChIKeyMKIJJIMOAABWGF-UHFFFAOYSA-N
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METHYL THIOGLYCOLATE
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