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CAS 22814-92-2

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4-(4-Chlorophenyl)-thiosemicarbazide

Description:
4-(4-Chlorophenyl)-thiosemicarbazide is an organic compound characterized by the presence of a thiosemicarbazide functional group, which consists of a thiocarbonyl group (C=S) bonded to a semicarbazide moiety. This compound features a chlorophenyl group, indicating the presence of a chlorine atom on a phenyl ring, which can influence its chemical reactivity and biological activity. It typically appears as a solid at room temperature and is soluble in polar solvents. The presence of the chlorine substituent can enhance the compound's lipophilicity and may affect its interaction with biological targets. Thiosemicarbazides are known for their diverse biological activities, including antimicrobial, antifungal, and anticancer properties, making compounds like 4-(4-Chlorophenyl)-thiosemicarbazide of interest in medicinal chemistry. Additionally, the compound may undergo various chemical reactions, such as oxidation or substitution, due to the reactivity of the thiosemicarbazide group. Safety data should be consulted for handling and potential hazards associated with this compound.
Formula:C7H8ClN3S
InChI:InChI=1/C7H8ClN3S/c8-5-1-3-6(4-2-5)10-7(12)11-9/h1-4H,9H2,(H2,10,11,12)
SMILES:c1cc(ccc1Cl)NC(=NN)S
Synonyms:
  • 4-(4-Chlorophenyl)-3-thiosemicarbazide
  • N-(4-chlorophenyl)hydrazinecarbothioamide
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