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Relevant bibliographies by topics / Phenoxyacetohydrazide

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Journal articles

Academic literature on the topic 'Phenoxyacetohydrazide'

Author: Grafiati

Published: 3 June 2025

Last updated: 31 July 2025

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Journal articles on the topic "Phenoxyacetohydrazide"

1

Fun, Hoong-Kun, Ching Kheng Quah, Arun M. Isloor, Dhanya Sunil, and Prakash Shetty. "2-Phenoxyacetohydrazide." Acta Crystallographica Section E Structure Reports Online 66, no. 1 (2009): o53—o54. http://dx.doi.org/10.1107/s1600536809051344.

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2

Jamil, Waqas, Shagufta Perveen, Syed Shah та ін. "Phenoxyacetohydrazide Schiff Bases: β-Glucuronidase Inhibitors". Molecules 19, № 7 (2014): 8788–802. http://dx.doi.org/10.3390/molecules19078788.

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3

Sangeetha, M., and R. Mathammal. "EXPERIMENTAL CUM THEORETICAL EVALUATION OF MOLECULAR STRUCTURE, VIBRATIONAL SPECTRA, NBO, UV, NMR, OF A BIOACTIVE COMPOUND – PHENOXYACETOHYDRAZIDE." International Journal of Research -GRANTHAALAYAH 3, no. 7 (2015): 103–15. http://dx.doi.org/10.29121/granthaalayah.v3.i7.2015.2991.

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Hydrazide-Hydrazone compounds are key species for a range of bioactivities. The first complete density functional theoretical study of Phenoxyacetohydrazide(PAH) is reported. The normal mode frequencies, intensities and the corresponding vibrational assignments were calculated using the GAUSSIAN 09W set of quantum chemistry codes at the DFT/B3LYP levels of theory using the 6-311++G** basis set. Stability of the molecule arising from hyperconjugative interactions has been probed using NBO analysis. 1H and 13C NMR spectra have been analysed and the chemical shifts were calculated using the gauge

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4

M., Sangeetha, and Mathammal R. "EXPERIMENTAL CUM THEORETICAL EVALUATION OF MOLECULAR STRUCTURE, VIBRATIONAL SPECTRA, NBO, UV, NMR, OF A BIOACTIVE COMPOUND – PHENOXYACETOHYDRAZIDE." International Journal of Research -GRANTHAALAYAH 3, no. 7 (2017): 103–15. https://doi.org/10.5281/zenodo.847084.

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Hydrazide-Hydrazone compounds are key species for a range of bioactivities. The first complete density functional theoretical study of Phenoxyacetohydrazide (PAH) is reported. The normal mode frequencies, intensities and the corresponding vibrational assignments were calculated using the GAUSSIAN 09W set of quantum chemistry codes at the DFT/B3LYP levels of theory using the 6-311++G** basis set. Stability of the molecule arising from hyperconjugative interactions has been probed using NBO analysis. 1H and 13C NMR spectra have been analysed and the chemical shifts were calculated using the gaug

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5

Tang, Yan-Ru. "(E)-N′-[1-(2-Hydroxyphenyl)ethylidene]-2-phenoxyacetohydrazide–2,2′-(1,1′-azinodiethylidyne)diphenol (2/1)." Acta Crystallographica Section E Structure Reports Online 67, no. 7 (2011): o1819. http://dx.doi.org/10.1107/s1600536811023956.

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6

Badawi, Hassan M. "Comparative study between the X-ray, DFT and Møller–Plesset structure of solid phenoxyacetohydrazide." Journal of Molecular Structure 984, no. 1-3 (2010): 209–13. http://dx.doi.org/10.1016/j.molstruc.2010.09.029.

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7

An, Caixia, Xilan Feng, Ning Zhao, Ping Liu, Tianxi Wang, and Zhaoxun Lian. "Synthesis, structures, and third-order nonlinear optical properties of three new copper complexes based on salicylaldehyde phenoxyacetohydrazide ligand." Journal of Coordination Chemistry 67, no. 22 (2014): 3621–32. http://dx.doi.org/10.1080/00958972.2014.976212.

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8

Solet, Sanwar Mal, Neetesh Kumar Sharma, and Raghvendra Singh Bhadauria. "Synthesis of 2, 5-disubstituted-1, 3, 4-oxadiazole derivatives." Journal of Drug Delivery and Therapeutics 9, no. 4-A (2019): 528–60. http://dx.doi.org/10.22270/jddt.v9i4-a.3514.

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Synthesis of a series of various 2, 5-disubstituted-1, 3, 4-oxadiazole derivatives (7a-7u) have been done. Synthesis of a series of intermediates (3a-3c and 5a-5c) have been also done, ethyl-2-phenoxyacetate (3a), ethyl 2-(2, 4-dichlorophenoxy)acetate (3b), ethyl 2-(4-nitrorophenoxy) acetate (3c), 2-phenoxyacetohydrazide (5a), 2-(2, 4-dichlorophenoxy) acetohydrazide (5b), 2-(4-nitrophenoxy)acetohydrazide (5c), and final product (7a-7u), 2-(phenoxymethyl)-5-phenyl-1, 3, 4-oxadiazole (7a), 4-(5-(phenoxymethyl)-1, 3, 4-oxadiazol-2-yl)aniline (7b), 3-(5-(phenoxymethyl)-1, 3, 4-oxadiazol-2-yl) anil

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9

Jupudi, Srikanth, Mohammed Afzal Azam, and Ashish Wadhwani. "Design, synthesis and molecular modelling of phenoxyacetohydrazide derivatives as Staphylococcus aureus MurD inhibitors." Chemical Papers, October 3, 2020. http://dx.doi.org/10.1007/s11696-020-01380-2.

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