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CAS 1086376-13-7

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5-[2-(2-Chloro-3,4-dimethoxyphenyl)ethenyl]-1,3,4-oxadiazol-2(3H)-one

Description:
5-[2-(2-Chloro-3,4-dimethoxyphenyl)ethenyl]-1,3,4-oxadiazol-2(3H)-one is a chemical compound characterized by its unique oxadiazole ring structure, which contributes to its potential biological activity. The presence of the chloro and methoxy substituents on the phenyl group enhances its lipophilicity and may influence its interaction with biological targets. This compound is likely to exhibit properties such as moderate to high stability under standard conditions, and its reactivity may be influenced by the electron-withdrawing nature of the chloro group and the electron-donating properties of the methoxy groups. The oxadiazole moiety is known for its applications in pharmaceuticals and agrochemicals, often associated with antimicrobial and anti-inflammatory activities. Additionally, the compound's molecular structure suggests potential for various synthetic modifications, which could lead to derivatives with enhanced efficacy or selectivity. As with many synthetic organic compounds, safety and handling precautions should be observed due to potential toxicity or reactivity.
Formula:C12H11ClN2O4
InChI:InChI=1S/C12H11ClN2O4/c1-17-8-5-3-7(10(13)11(8)18-2)4-6-9-14-15-12(16)19-9/h3-6H,1-2H3,(H,15,16)
InChI key:InChIKey=SWTRYUZXMWVSSM-UHFFFAOYSA-N
SMILES:C(=CC=1OC(=O)NN1)C2=C(Cl)C(OC)=C(OC)C=C2
Synonyms:
  • 1,3,4-Oxadiazol-2(3H)-one, 5-[2-(2-chloro-3,4-dimethoxyphenyl)ethenyl]-
  • 5-[2-(2-Chloro-3,4-dimethoxyphenyl)ethenyl]-1,3,4-oxadiazol-2(3H)-one
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