Weight | 76.12 g/mol |
---|---|
Formula | C2H4OS |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
THIOACETIC ACID
thioacetic acid, potassium salt · thioacetic acid, sodium salt
507-09-5, 68-11-1, 10387-40-3
Score:
#1189 in Physics
,
#3392 in Chemistry
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- Enantioselective Addition of Thioacetic Acid to Nitroalkenes via N-Sulfinyl Urea Organocatalysis (Journal of the American Chemical Society, 2009)
- Mechanistic Study of Photoinitiated Free Radical Polymerization Using Thioxanthone Thioacetic Acid as One-Component Type II Photoinitiator (Macromolecules, 2005)
- Organocatalytic Asymmetric Conjugate Addition of Thioacetic Acid to -Nitrostyrenes. (Tetrahedron Letters, 2006)
- Organocatalytic enantioselective michael addition of thioacetic acid to enones (Tetrahedron Letters, 2006)
- Squaramide-catalysed enantio- and diastereoselective sulfa-Michael addition of thioacetic acid to ,-disubstituted nitroalkenes. (Organic and Biomolecular Chemistry, 2012)
- Phosphoric Acid Catalyzed Asymmetric 1,6-Conjugate Addition of Thioacetic Acid to para-Quinone Methides (Angewandte Chemie, 2016)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - thioacetic acid, potassium salt
- thioacetic acid, sodium salt
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SMILESCC(=O)S
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InChIKeyDUYAAUVXQSMXQP-UHFFFAOYSA-N
- Pubchem - THIOACETIC ACID
- Wikipedia - thioacetic acid
Thioacetic acid is an organosulfur compound with the molecular formula CH3COSH. It is a yellow coloured liquid with a strong thiol-like odor. It is used in organic synthesis for the introduction of thiol groups in molecules
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