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CAS 13124-11-3

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4-(2,4-Dichlorophenyl)-3-thiosemicarbazide

Description:
4-(2,4-Dichlorophenyl)-3-thiosemicarbazide is an organic compound characterized by its thiosemicarbazide functional group, which features a sulfur atom bonded to a carbonyl carbon. This compound contains a dichlorophenyl moiety, indicating the presence of two chlorine atoms on a phenyl ring, specifically at the 2 and 4 positions. The thiosemicarbazide structure contributes to its potential biological activity, as thiosemicarbazides are known for their roles in medicinal chemistry, particularly as antimicrobial and anticancer agents. The presence of the dichlorophenyl group may enhance its lipophilicity and biological interactions. This compound is typically a solid at room temperature and may exhibit moderate solubility in organic solvents. Its reactivity can be influenced by the electron-withdrawing nature of the chlorine substituents, which can affect its nucleophilicity and overall chemical behavior. As with many thiosemicarbazides, it may also participate in various chemical reactions, including condensation and complexation with metal ions, making it of interest in coordination chemistry and drug development.
Formula:C7H7Cl2N3S
InChI:InChI=1/C7H7Cl2N3S/c8-4-1-2-6(5(9)3-4)11-12-7(10)13/h1-3,11H,(H3,10,12,13)
SMILES:c1cc(c(cc1Cl)Cl)NNC(=N)S
Synonyms:
  • N-(2,4-dichlorophenyl)hydrazinecarbothioamide
  • 2-(2,4-Dichlorophenyl)Hydrazinecarbothioamide
  • 2,4-DICHLOROPHENYLTHIOSEMICARBAZIDE
  • 2-(2,4-DICHLOROPHENYL)-1-HYDRAZINECARBOTHIOAMIDE
  • 4-(2,4-DICHLOROPHENYL)-3-THIOSEMICARBAZIDE
  • 4-(2,4-DICHLOROPHENYL)-3-THIOSEMICARBAZIDE, 98+%
  • 1-(2,4-Dichlorophenyl)thiosemicarbazide
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