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CAS 21198-18-5

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4-Cyclohexylthiosemicarbazide

Description:
4-Cyclohexylthiosemicarbazide is an organic compound characterized by its thiosemicarbazide functional group, which features a sulfur atom bonded to a semicarbazide moiety. This compound typically appears as a white to off-white solid and is known for its potential applications in medicinal chemistry, particularly in the development of pharmaceuticals due to its biological activity. The presence of the cyclohexyl group contributes to its hydrophobic characteristics, influencing its solubility and interaction with biological systems. 4-Cyclohexylthiosemicarbazide may exhibit properties such as antimicrobial, antifungal, or anticancer activities, making it a subject of interest in research. Its reactivity can be attributed to the presence of functional groups that allow for various chemical transformations. Safety data should be consulted, as with any chemical, to understand its handling, storage, and potential hazards. Overall, this compound represents a versatile scaffold in organic synthesis and drug development.
Formula:C7H15N3S
InChI:InChI=1S/C7H15N3S/c8-10-7(11)9-6-4-2-1-3-5-6/h6H,1-5,8H2,(H2,9,10,11)
InChI key:InChIKey=LVEUHPMMNLURRJ-UHFFFAOYSA-N
SMILES:N(C(NN)=S)C1CCCCC1
Synonyms:
  • 1-Amino-3-cyclohexylthiourea
  • 1-Cyclohexylhydrazinecarbothioamide
  • 3-Amino-1-cyclohexylthiourea
  • 4-Cyclohexyl-3-thiosemicarbazide
  • 4-Cyclohexylthiosemicarbazide
  • Hydrazinecarbothioamide, N-cyclohexyl-
  • N-Cyclohexylthiosemicarbazide
  • N-cyclohexylhydrazinecarbothioamide
  • NSC 82337
  • Semicarbazide, 4-cyclohexyl-3-thio-
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