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CAS 6610-36-2

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4-(4-Chlorobenzyl)-thiosemicarbazide

Description:
4-(4-Chlorobenzyl)-thiosemicarbazide is an organic compound characterized by its thiosemicarbazide functional group, which features a sulfur atom bonded to a carbonyl group and an amine. This compound typically appears as a solid and is known for its potential biological activities, including antimicrobial and anticancer properties. The presence of the 4-chlorobenzyl group enhances its lipophilicity, which may influence its interaction with biological membranes and its overall pharmacological profile. It is soluble in polar organic solvents, and its reactivity can be attributed to the presence of the thiosemicarbazide moiety, which can participate in various chemical reactions, including condensation and coordination with metal ions. The compound's structure allows for potential modifications, making it a subject of interest in medicinal chemistry and drug development. Safety data should be consulted, as with any chemical, to understand its handling and toxicity profiles.
Formula:C26H20N4O3S
InChI:InChI=1/C26H20N4O3S/c1-15-18(25-29-23-21(33-25)11-6-12-27-23)9-5-10-20(15)28-26(34)30-24(31)19-13-16-7-3-4-8-17(16)14-22(19)32-2/h3-14H,1-2H3,(H2,28,30,31,34)
SMILES:Cc1c(cccc1N=C(N=C(c1cc2ccccc2cc1OC)O)S)c1nc2c(cccn2)o1
Synonyms:
  • 3-methoxy-N-{[2-methyl-3-([1,3]oxazolo[4,5-b]pyridin-2-yl)phenyl]carbamothioyl}naphthalene-2-carboxamide
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