CAS 22536-46-5

[(2-oxo-2-phenylethyl)sulfanyl]acetic acid

Description:

[(2-oxo-2-phenylethyl)sulfanyl]acetic acid, with the CAS number 22536-46-5, is an organic compound characterized by the presence of a sulfanyl group (-S-) attached to an acetic acid moiety. This compound features a phenyl group, which contributes to its aromatic properties, and a keto group (C=O) adjacent to the sulfanyl linkage. The structure suggests that it may exhibit both acidic and nucleophilic characteristics due to the carboxylic acid functional group and the presence of the sulfur atom, which can participate in various chemical reactions. The compound is likely to be soluble in polar solvents, given the presence of the carboxylic acid, and may exhibit biological activity, making it of interest in medicinal chemistry. Its reactivity can be influenced by the electron-withdrawing nature of the carbonyl group and the electron-donating properties of the phenyl ring. Overall, this compound's unique structure may lead to diverse applications in organic synthesis and pharmaceutical development.

Formula: C₁₀H₁₀O₃S

InChI: InChI=1/C10H10O3S/c11-9(6-14-7-10(12)13)8-4-2-1-3-5-8/h1-5H,6-7H2,(H,12,13)

SMILES: c1ccc(cc1)C(=O)CSCC(=O)O

Synonyms:

• Acetic Acid, 2-[(2-Oxo-2-Phenylethyl)Thio]-

[(2-Oxo-2-phenylethyl)sulfanyl]acetic acid

CAS: 22536-46-5

[(2-Oxo-2-phenylethyl)sulfanyl]acetic acid is a methyl ester that belongs to the class of alpha,alpha-diphenylacetates. It has been shown to be an effective inhibitor of protein synthesis in bacteria and yeast. This inhibition may be due to its ability to inhibit ribosome function by binding to the 30S subunit of bacterial ribosomes. The acid methyl ester form of [(2-Oxo-2-phenylethyl)sulfanyl]acetic acid is also an inhibitor of protein synthesis in bacteria and yeast, but it does not inhibit ribosome function.

Formula: C₁₀H₁₀O₃S

Purity: Min. 95%

Molecular weight: 210.25 g/mol

Ref: 3D-XAA53646