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CAS 6320-49-6

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5-[(5-Chloro-2-hydroxyphenyl)methylene]-2-thioxo-4-thiazolidinone

Description:
5-[(5-Chloro-2-hydroxyphenyl)methylene]-2-thioxo-4-thiazolidinone, with the CAS number 6320-49-6, is a thiazolidinone derivative characterized by its thiazolidine ring structure, which incorporates a thione functional group. This compound features a chloro-substituted phenolic moiety, contributing to its potential biological activity. The presence of the thioxo group suggests that it may exhibit reactivity typical of thioketones, which can participate in various chemical reactions, including nucleophilic attacks. The hydroxyl group on the aromatic ring enhances its solubility in polar solvents and may influence its interaction with biological targets. This compound has garnered interest in medicinal chemistry for its potential pharmacological properties, including antimicrobial and anti-inflammatory activities. Its unique structural features may also allow for further modifications to enhance efficacy or reduce toxicity. As with many thiazolidinone derivatives, the compound's stability, reactivity, and biological activity can be influenced by environmental factors such as pH and temperature, making it a subject of interest for further research in drug development and synthetic chemistry.
Formula:C10H6ClNO2S2
InChI:InChI=1S/C10H6ClNO2S2/c11-6-1-2-7(13)5(3-6)4-8-9(14)12-10(15)16-8/h1-4,13H,(H,12,14,15)
InChI key:InChIKey=OYUGKKNIIOTAPN-UHFFFAOYSA-N
SMILES:C(=C1C(=O)NC(=S)S1)C2=C(O)C=CC(Cl)=C2
Synonyms:
  • (5E)-5-(5-chloro-2-hydroxybenzylidene)-2-sulfanyl-1,3-thiazol-4(5H)-one
  • 4(5H)-thiazolone, 5-[(5-chloro-2-hydroxyphenyl)methylene]-2-mercapto-, (5E)-
  • 4-Thiazolidinone, 5-[(5-chloro-2-hydroxyphenyl)methylene]-2-thioxo-
  • 5-[(5-Chloro-2-hydroxyphenyl)methylene]-2-thioxo-4-thiazolidinone
  • NSC 31201
  • Rhodanine, 5-(5-chlorosalicylidene)-
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