CAS 111874-19-2

Ethyl 2-(2-mercapto-4-methyl-1,3-thiazol-5-yl)acetate

Description:

Ethyl 2-(2-mercapto-4-methyl-1,3-thiazol-5-yl)acetate is an organic compound characterized by its thiazole ring, which contributes to its biological activity and potential applications in pharmaceuticals. The presence of a mercapto group (-SH) enhances its reactivity, making it useful in various chemical reactions, including nucleophilic substitutions. This compound typically appears as a colorless to pale yellow liquid and has a distinctive odor. Its molecular structure includes an ethyl ester functional group, which can influence its solubility and volatility. Ethyl 2-(2-mercapto-4-methyl-1,3-thiazol-5-yl)acetate may exhibit antimicrobial and antifungal properties, making it of interest in medicinal chemistry. Additionally, its thiazole moiety is often associated with various biological activities, including enzyme inhibition and interaction with biological targets. Safety data should be consulted for handling and exposure guidelines, as compounds containing thiol groups can be sensitive to oxidation and may pose health risks. Overall, this compound represents a versatile building block in organic synthesis and medicinal chemistry.

Formula: C₈H₁₁NO₂S₂

InChI: InChI=1/C8H11NO2S2/c1-3-11-7(10)4-6-5(2)9-8(12)13-6/h3-4H2,1-2H3,(H,9,12)

SMILES: CCOC(=O)Cc1c(C)nc(S)s1

Synonyms:

• 2,3-Dihydro-4-methyl-2-thioxo-5-thiazoleacetic acid ethyl ester
• 2-Sulfhydyl-4-Methyl-5-Thiazylethylformate
• Ethyl (4-Methyl-2-Sulfanyl-1,3-Thiazol-5-Yl)Acetate
• ethyl 2-(4-methyl-2-thioxo-2,3-dihydrothiazol-5-yl)acetate
• 2-(4-methyl-2-sulfanylidene-3H-thiazol-5-yl)acetic acid ethyl ester
• 2-Mercapto-4-methylthiazole-5-acetic acid ethyl ester
• Ethyl 2-(2-mercapto-4-methyl-1,3-thiazol-5-yl)acetate
• Ethyl 2-(2-Mercapto-4-Methylthiazol-5-yl)acetate
• 5-Thiazoleacetic acid, 2,3-dihydro-4-methyl-2-thioxo-, ethyl ester