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CAS 5706-80-9

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4-Chlorobenzaldehyde thiosemicarbazone

Description:
4-Chlorobenzaldehyde thiosemicarbazone is an organic compound characterized by its thiosemicarbazone functional group, which is derived from the condensation of 4-chlorobenzaldehyde and thiosemicarbazide. This compound typically appears as a solid and is known for its potential biological activities, including antimicrobial and anticancer properties. It features a chlorinated aromatic ring, which contributes to its reactivity and interaction with biological systems. The presence of the thiosemicarbazone moiety enhances its ability to form coordination complexes with metal ions, making it of interest in coordination chemistry. Additionally, 4-Chlorobenzaldehyde thiosemicarbazone can exhibit various physical properties, such as solubility in organic solvents, which may vary based on the solvent's polarity. Its synthesis often involves straightforward laboratory procedures, making it accessible for research purposes. As with many thiosemicarbazones, it may also display tautomeric behavior, which can influence its chemical reactivity and stability. Overall, this compound serves as a valuable subject for studies in medicinal chemistry and coordination chemistry.
Formula:C8H8ClN3S
InChI:InChI=1S/C8H8ClN3S/c9-7-3-1-6(2-4-7)5-11-12-8(10)13/h1-5H,(H3,10,12,13)
InChI key:InChIKey=FABQYDLGFZXBIK-UHFFFAOYSA-N
SMILES:C(=NNC(N)=S)C1=CC=C(Cl)C=C1
Synonyms:
  • 2-(4-Chlorobenzylidene)hydrazine-1-carbothioamide
  • 2-[(4-Chlorophenyl)methylene]hydrazinecarbothioamide
  • 4-Chlorobenzaldehyde thiosemicarbazone
  • Benzaldehyde, p-chloro-, thiosemicarbazone
  • Hydrazinecarbothioamide, 2-[(4-Chlorophenyl)Methylene]-
  • NSC 8277
  • p-Chlorobenzaldehyde thiosemicarbazone
  • 2-(4-Chlorobenzylidene)hydrazinecarbothioamide
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