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CAS 23766-28-1

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2-Mercapto-5-(4-chlorophenyl)-1,3,4-oxadiazole

Description:
2-Mercapto-5-(4-chlorophenyl)-1,3,4-oxadiazole is a chemical compound characterized by its unique structure, which includes a mercapto group (-SH) and an oxadiazole ring. This compound features a chlorophenyl substituent, which enhances its potential biological activity. The presence of the thiol group contributes to its reactivity, making it a candidate for various chemical reactions, including nucleophilic substitutions and redox processes. The oxadiazole moiety is known for its applications in pharmaceuticals and agrochemicals due to its ability to act as a bioactive scaffold. Additionally, the chlorophenyl group can influence the compound's lipophilicity and overall pharmacokinetic properties. This substance may exhibit antimicrobial, antifungal, or anticancer activities, although specific biological data would be necessary to confirm these effects. As with many chemical compounds, safety and handling precautions should be observed, particularly due to the presence of the thiol group, which can be reactive and potentially hazardous.
Formula:C8H5ClN2OS
InChI:InChI=1S/C8H5ClN2OS/c9-6-3-1-5(2-4-6)7-10-11-8(13)12-7/h1-4H,(H,11,13)
InChI key:InChIKey=MUFWSGAENICYQA-UHFFFAOYSA-N
SMILES:S=C1OC(C2=CC=C(Cl)C=C2)=NN1
Synonyms:
  • 1,3,4-Oxadiazole-2(3H)-thione, 5-(4-chlorophenyl)-
  • 1,3,4-Oxadiazole-2-thiol, 5-(4-chlorophenyl)-
  • 1,3,4-Oxadiazole-2-thiol, 5-(p-chlorophenyl)-
  • 2-(4-Chlorophenyl)-5-mercapto-1,3,4-oxadiazole
  • 2-(4-Chlorophenyl)-Δ<sup>2</sup>-1,3,4-oxadiazoline-5-thione
  • 2-Mercapto-5-(4-chlorophenyl)-1,3,4-oxadiazole
  • 5-(4-Chlorophenyl)-1,3,4-oxadiaole-2-thiol
  • 5-(4-Chlorophenyl)-1,3,4-oxadiazole-2(3H)-thione
  • 5-(4-Chlorophenyl)-2-thioxo-1,3,4-oxadiazoline
  • 5-(p-Chlorophenyl)-1,3,4-oxadiazole-2-thione
  • 5-(p-Chlorophenyl)-2-mercapto-1,3,4-oxadiazole
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