Description

S-Phenyl thioacetate (CAS No. 934-87-2), also known as S-phenyl ethanethioate, is a high-purity organosulfur compound with the molecular formula C₈H₈OS. This versatile reagent features a thioester functional group, where an acetyl group is bonded to a sulfur atom that is further linked to a phenyl ring. Its unique structure makes it valuable in organic synthesis, particularly in the preparation of sulfur-containing compounds and as a building block in pharmaceuticals, agrochemicals, and material science applications. Our product is rigorously tested to ensure exceptional quality, with purity levels suitable for demanding research and industrial processes. Available in various quantities, it is supplied in secure, chemically resistant packaging to maintain stability and shelf life.

Properties

• CAS Number: 934-87-2
• Complexity: 116
• IUPAC Name: S-phenyl ethanethioate
• InChI: InChI=1S/C8H8OS/c1-7(9)10-8-5-3-2-4-6-8/h2-6H,1H3
• InChI Key: WBISVCLTLBMTDS-UHFFFAOYSA-N
• Exact Mass: 152.02958605
• Molecular Formula: C8H8OS
• Molecular Weight: 152.22
• SMILES: CC(=O)SC1=CC=CC=C1
• Topological: 42.4
• Monoisotopic Mass: 152.02958605
• Synonyms: S-Phenyl thioacetate, 934-87-2, S-Phenyl ethanethioate, Thiophenyl acetate, S-PHENYLTHIOACETATE, Ethanethioic acid, S-phenyl ester, ACETIC ACID, THIO-, S-PHENYL ESTER, Phenyl thiolacetate, Thioacetic acid S-phenyl ester, 1-(phenylsulfanyl)ethan-1-one, L1K5I18NJ8, EINECS 213-294-2, BRN 1858641, AI3-15532, MFCD00008752, 1-phenylsulfanylethanone, S-Phenyl ethanethioate #, BENZENETHIOL, ACETATE, UNII-L1K5I18NJ8, S-Phenyl thioacetate, 98%, 4-06-00-01522 (Beilstein Handbook Reference), SCHEMBL342299, SCHEMBL1979861, SCHEMBL2039663, SCHEMBL6972687, ethanethioic acid S-phenyl ester, SCHEMBL16116058, WBISVCLTLBMTDS-UHFFFAOYSA-, DTXSID00239419, AKOS015840643, BS-23840, NS00039567, T0849, InChI=1/C8H8OS/c1-7(9)10-8-5-3-2-4-6-8/h2-6H,1H3

Application

S-Phenyl thioacetate is widely used as a key intermediate in organic synthesis, particularly for introducing thioester functionalities into target molecules. It serves as a precursor in the preparation of sulfur-containing heterocycles and is employed in peptide chemistry for thioacetylation reactions. Researchers also utilize it in the development of novel agrochemicals and pharmaceuticals due to its reactivity and structural versatility.

If you are interested or have any questions, please contact us at support@atomfair.com

Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.