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CAS 57658-21-6

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3-(5-Mercapto-1,3,4-thiadiazol-2-ylthio)-propionic acid

Description:
3-(5-Mercapto-1,3,4-thiadiazol-2-ylthio)-propionic acid, with the CAS number 57658-21-6, is a chemical compound that features a thiadiazole ring, which is known for its diverse biological activities. This compound contains a propionic acid moiety, contributing to its acidic properties. The presence of a mercapto group (-SH) enhances its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions. The thiadiazole structure is often associated with antimicrobial and antifungal properties, suggesting potential applications in pharmaceuticals or agricultural chemicals. Additionally, the compound's ability to form disulfide bonds may play a role in its biological interactions. Its solubility characteristics can vary based on the pH of the environment, which is important for its application in biological systems. Overall, this compound exemplifies the intersection of organic chemistry and medicinal applications, warranting further investigation into its properties and potential uses in various fields.
Formula:C5H6N2O2S3
InChI:InChI=1/C5H6N2O2S3/c8-3(9)1-2-11-5-7-6-4(10)12-5/h1-2H2,(H,6,10)(H,8,9)
SMILES:C(CSc1nnc(S)s1)C(=O)O
Synonyms:
  • 3-[(5-Thioxo-4,5-Dihydro-1,3,4-Thiadiazol-2-Yl)Sulfanyl]Propanoic Acid
  • 3-(5-MERCAPTO-1,3,4-THIADIAZOL-2-YLTHIO)PROPIONIC ACID
  • Propanoic acid, 3-[(4,5-dihydro-5-thioxo-1,3,4-thiadiazol-2-yl)thio]-
  • 3-(5-Mercapto-1,3,4-thiadiazol-2-ylthio)propionic
  • Propionicacid, 3-(5-Mercapto-1,3,4-thiadiazol-2-ylthio)- (6CI)
  • 3-[(5-MERCAPTO-1,3,4-THIADIAZOL-2-YL)THIO]PROPANOIC ACID
  • 3-[(5-SULFANYL-1,3,4-THIADIAZOL-2-YL)SULFANYL]PROPANOIC ACID
  • 3-[(2-sulfanylidene-3H-1,3,4-thiadiazol-5-yl)sulfanyl]propanoic acid
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