Thioacetic acid (C007B-279296)

Thioacetic acid (TAA) can undergo:• Enantioselective addition to nitroalkenes to form chiral 1,2-aminothiol derivatives in the presence of a novel sulfinyl urea organocatalyst. This method has been successfully employed in the synthesis of antifungal drug, sulconazole.• Asymmetric Michael addition reaction with chalcones in the presence of a bifunctional amine thiourea catalyst to form synthetically useful thioesters.• Asymmetric 1,6-conjugate addition with para-quinone methides in the presence of a chiral phosphoric acid catalyst to form chiral sulfur-containing diphenylmethane-type compounds.• Conjugate addition to methacrylamides with chiral trans-2,5-disubstituted pyrrolidine auxiliaries to form chiral β-mercaptocarboxylic acid derivatives.Thioacetic acid is a reagent for introduction of the thiol group into organic molecules.A reagent for introduction of the thiol group into organic molecules.

Specifications and Purity: ≥95%

MDL Number: MFCD00004853

Molecular Formula: C2H4OS

Molecular Weight: 76.12

EC Number: 208-063-8

PubChem CID: 10484

Isomeric SMILES: CC(=O)S

Beilstein Registry Number: 2230

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