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CAS 78862-75-6

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4-(3-Chloro-4-methylphenyl)-3-thiosemicarbazide

Description:
4-(3-Chloro-4-methylphenyl)-3-thiosemicarbazide is a chemical compound characterized by its thiosemicarbazide functional group, which is known for its potential biological activity. This compound features a chloro-substituted aromatic ring, contributing to its unique reactivity and interaction with biological systems. The presence of the thiosemicarbazide moiety suggests potential applications in medicinal chemistry, particularly in the development of antimicrobial or anticancer agents, as thiosemicarbazides are often investigated for their pharmacological properties. The compound is typically solid at room temperature and may exhibit moderate solubility in organic solvents. Its molecular structure allows for various chemical modifications, which can enhance its biological efficacy or alter its physicochemical properties. Safety data should be consulted for handling, as compounds with halogen substituents can sometimes pose toxicity risks. Overall, 4-(3-Chloro-4-methylphenyl)-3-thiosemicarbazide represents a class of compounds with significant interest in both synthetic and medicinal chemistry.
Formula:C8H10ClN3S
InChI:InChI=1/C8H10ClN3S/c1-5-2-3-6(4-7(5)9)11-8(13)12-10/h2-4H,10H2,1H3,(H2,11,12,13)
SMILES:Cc1ccc(cc1Cl)N=C(NN)S
Synonyms:
  • N-(3-chloro-4-methylphenyl)hydrazinecarbothioamide
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