Design, Synthesis, and In-Depth Biological Assessment of Novel 2-[(E)-2-Substituted-Ethenyl]-1,3-Benzoxazole Derivatives

  • Unique Paper ID: 184294
  • PageNo: 904-912
  • Abstract:
  • Using 2-methylbenzoxazole derivatives and suitably substituted aldehydes, a systematic condensation procedure was used to create a novel series of 2-[(E)-2-substituted-ethenyl] derivatives of 1,3-benzoxazoles. Mass spectrometry, FT-IR, ¹H NMR, ¹³C NMR, and other spectroscopic methods were used to confirm the molecular frameworks and stereochemistry of the produced compounds. Their antibacterial, antioxidant, and cytotoxic properties were evaluated through a thorough biological analysis. Numerous compounds showed excellent antioxidant activity in DPPH experiments and noteworthy antibacterial potency against both Gram-positive and Gram-negative bacterial strains, indicating significant biological value. The crucial impact of electron-donating and electron-withdrawing substituents on biological outcomes was demonstrated by the structure-activity relationship (SAR) research. According to these results, 2-[(E)-2-substituted-ethenyl]-1,3-benzoxazole compounds have a great deal of promise as therapeutic scaffolding for additional drug development.

Copyright & License

Copyright © 2026 Authors retain the copyright of this article. This article is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

BibTeX

@article{184294,
        author = {Mohammad Zaid Mansoori and DR REETESH YADAV and DR DEEPAK PATEL and DILEND PATLE},
        title = {Design, Synthesis, and In-Depth Biological Assessment of Novel 2-[(E)-2-Substituted-Ethenyl]-1,3-Benzoxazole Derivatives},
        journal = {International Journal of Innovative Research in Technology},
        year = {2025},
        volume = {12},
        number = {4},
        pages = {904-912},
        issn = {2349-6002},
        url = {https://ijirt.org/article?manuscript=184294},
        abstract = {Using 2-methylbenzoxazole derivatives and suitably substituted aldehydes, a systematic condensation procedure was used to create a novel series of 2-[(E)-2-substituted-ethenyl] derivatives of 1,3-benzoxazoles. Mass spectrometry, FT-IR, ¹H NMR, ¹³C NMR, and other spectroscopic methods were used to confirm the molecular frameworks and stereochemistry of the produced compounds. Their antibacterial, antioxidant, and cytotoxic properties were evaluated through a thorough biological analysis. Numerous compounds showed excellent antioxidant activity in DPPH experiments and noteworthy antibacterial potency against both Gram-positive and Gram-negative bacterial strains, indicating significant biological value. The crucial impact of electron-donating and electron-withdrawing substituents on biological outcomes was demonstrated by the structure-activity relationship (SAR) research. According to these results, 2-[(E)-2-substituted-ethenyl]-1,3-benzoxazole compounds have a great deal of promise as therapeutic scaffolding for additional drug development.},
        keywords = {DPPH, 2-methylbenzoxazole, 1,3-benzoxazoles, Mass spectrometry, 2-[(E)-2-substituted-ethenyl]-1,3-benzoxazole, Antibacterial. Antioxidant Activity Assays, Synthesis, and Characterization},
        month = {September},
        }

Cite This Article

Mansoori, M. Z., & YADAV, D. R., & PATEL, D. D., & PATLE, D. (2025). Design, Synthesis, and In-Depth Biological Assessment of Novel 2-[(E)-2-Substituted-Ethenyl]-1,3-Benzoxazole Derivatives. International Journal of Innovative Research in Technology (IJIRT), 12(4), 904–912.

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