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Relevant bibliographies by topics / Methylacetophenone

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Academic literature on the topic 'Methylacetophenone'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "Methylacetophenone"

1

Amaral, Luísa M. P. F., and Manuel A. V. Ribeiro da Silva. "Calorimetric study of 2′-methylacetophenone and 4′-methylacetophenone." Journal of Chemical Thermodynamics 57 (February 2013): 301–5. http://dx.doi.org/10.1016/j.jct.2012.08.034.

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2

Espinosa-Colín, María, Irene Hernandez-Caballero, Celia Infante, Irene Gago, Javier García-Muñoz, and Teresa Sosa. "Evaluation of Propiophenone, 4-Methylacetophenone and 2′,4′-Dimethylacetophenone as Phytotoxic Compounds of Labdanum Oil from Cistus ladanifer L." Plants 12, no. 5 (2023): 1187. http://dx.doi.org/10.3390/plants12051187.

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This is the first study to evaluate the phytotoxic activity of three phenolic compounds present in the essential oil of the labdanum of Cistus ladanifer, an allelopathic species of the Mediterranean ecosystem. Propiophenone, 4′-methylacetophenone, and 2′,4′-dimethylacetophenone slightly inhibit total germination and radicle growth of Lactuca sativa, and they strongly delay germination and reduce hypocotyl size. On the other hand, the inhibition effect of these compounds on Allium cepa was stronger on total germination than on germination rate, and radicle length compared to hypocotyl size. The

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3

Z Sharkawi, Marco M., Norhan R. Mohamed, Mohammed T. El-Saadi, and Noha H. Amin. "Validated green chromatographic methods for determination of amlodipine and celecoxib in presence of methylacetophenone." Bioanalysis 13, no. 12 (2021): 969–83. http://dx.doi.org/10.4155/bio-2021-0040.

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Aim: Green, accurate and rapid methods, namely LC–MS/MS and thin layer chromatography-densitometric methods, were developed for determination of amlodipine besylate and celecoxib in presence of its process-related impurities, 4-methylacetophenone in pure and formulated tablets. Results: LC–MS/MS was achieved on ZORBAX Eclipse Plus C18 column using methanol:aqueous solution of 5 mM formic acid (95:5 v/v). High sensitivity with low limit of detection values 0.00028, 0.00027 and 0.0003 for amlodipine, celecoxib and 4-methylacetophenone, respectively were obtained. While, thin layer chromatography

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4

Chanysheva, A. R., A. L. Sufiyarova, N. V. Privalov, and V. V. Zorin. "Green Asymmetric Reduction of Methylacetophenone." Russian Journal of General Chemistry 92, no. 13 (2022): 3111–15. http://dx.doi.org/10.1134/s1070363222130126.

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5

Evans, S. V., та J. Trotter. "Structure of α-cycloheptyl-4-methylacetophenone". Acta Crystallographica Section C Crystal Structure Communications 44, № 8 (1988): 1459–62. http://dx.doi.org/10.1107/s0108270188004263.

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6

Su, Shih-Hao, and Ming-Der Su. "Mechanistic analysis of the photochemical carboxylation of o-alkylphenyl ketones with carbon dioxide." RSC Advances 6, no. 56 (2016): 50825–32. http://dx.doi.org/10.1039/c6ra05890f.

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The mechanisms for photochemical carboxylation reactions are studied theoretically using two model systems: o-methylbenzophenone and o-methylacetophenone, with the M06-L and the 6-311G(d,p) basis set.

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7

Liotier, Elodie, Guy Mousset, and Christine Mousty. "Electrochemical and spectroscopic behavior of trifluoromethylacetophenone in aqueous and micellar medium." Canadian Journal of Chemistry 73, no. 9 (1995): 1488–96. http://dx.doi.org/10.1139/v95-184.

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The electrochemical behavior of 4-trifluoromethylacetophenone (TFMA) has been studied in aqueous (2 ≤ pH ≤ 10), micellar, and ethanolic solutions using polarographic techniques. A slow hydration process of the carbonyl group has been observed by means of polarography and UV–visible spectrophotometry. Besides the well-known pH dependence of the electroreduction of aromatic ketones, C—F bond cleavages concomitant to the ketone reduction occur under electrolysis conditions in alkaline medium (pH = 10) at a very negative potential (−1.7 V), leading to the formation of 4-methylacetophenone, which i

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8

K., K. ARAVINDAKSHAN. "Complexes of lron(III), Cobalt(II), Nickel(II), Zine(ll), Cadmium(II) and Mercury(II) with 2-Hydroxy-5 methylacetophenone Thiosemicarbazone." Journal of Indian Chemical Society Vol. 66, May 1989 (1989): 338–40. https://doi.org/10.5281/zenodo.6163954.

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Department or Chemistry, University of Calicut, Kerala-673 635 <em>Manuscript received 18 March 1988, revised 9 November 1988, accepted 28 February 1989</em> Complexes of lron(III), Cobalt(II), Nickel(II), Zine(ll), Cadmium(II) and Mercury(II) with 2-Hydroxy-5 methylacetophenone Thiosemicarbazone 

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9

K., K. ARAVINDAKSHAN, and MURALBEDHARAN K. "Thermal Decomposition and Kinetics of Cobalt(II) and Nickel(II) Complexes with 2-Hydroxy-5-methylacetophenone Thiosemicarbazone." Journal of Indian Chemical Society Vol. 68, Jun 1991 (1991): 348–50. https://doi.org/10.5281/zenodo.6156298.

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Department of Chemistry. University of Calicut. Kerala-673 635 <em>Manuscript received 25 October 1990, revised 6 May 1991, </em><em>accepted 27 May 1991</em> Thermal Decomposition and Kinetics of Cobalt(II) and Nickel(II) Complexes with 2-Hydroxy-5-methylacetophenone Thiosemicarbazone.

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10

Chakkaravarthi, G., A. Anthonysamy, S. Balasubramanian, and V. Manivannan. "4,4′-Dimethyl-2,2′-[1,1′-(ethane-1,2-diyldinitrilo)diethylidyne]diphenol." Acta Crystallographica Section E Structure Reports Online 63, no. 11 (2007): o4475. http://dx.doi.org/10.1107/s1600536807052622.

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The title compound, C20H24N2O2, is a Schiff base compound derived from the condensation of 2-hydroxy-5-methylacetophenone and 1,2-diaminoethane in ethanol. The molecule has crystallographic twofold rotation symmetry. The molecular structure is stabilized by weak intramolecular O—H...N interactions and the crystal packing is stabilized by weak intermolecular C—H...O and C—H...π interactions.

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Book chapters on the topic "Methylacetophenone"

1

Wohlfarth, Ch. "Viscosity of p-methylacetophenone." In Supplement to IV/18. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_315.

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2

Wohlfarth, Christian. "Viscosity of p-methylacetophenone." In Viscosity of Pure Organic Liquids and Binary Liquid Mixtures. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49218-5_315.

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3

Wohlfarth, Ch. "Viscosity of the mixture (1) acetonitrile; (2) p-methylacetophenone." In Supplement to IV/18. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_716.

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4

Wohlfarth, Ch. "Viscosity of the mixture (1) N-methylacetamide; (2) p-methylacetophenone." In Supplement to IV/18. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_960.

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5

Wohlfarth, Ch. "Dielectric constant of the mixture (1) benzene; (2) 4-methylacetophenone." In Supplement to IV/6. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75506-7_948.

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6

Wohlfarth, Ch. "Viscosity of the mixture (1) N,N-dimethylformamide; (2) p-methylacetophenone." In Supplement to IV/18. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75486-2_959.

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7

Wohlfarth, Ch. "Dielectric constant of the mixture (1) 1,4-dioxane; (2) 4-methylacetophenone." In Supplement to IV/6. Springer Berlin Heidelberg, 2008. http://dx.doi.org/10.1007/978-3-540-75506-7_764.

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8

Wohlfarth, Christian. "Viscosity of the binary liquid mixture of N-ethylaniline and p-methylacetophenone." In Viscosity of Pure Organic Liquids and Binary Liquid Mixtures. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49218-5_1859.

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9

Wohlfarth, Christian. "Viscosity of the binary liquid mixture of N,N-dimethylaniline and p-methylacetophenone." In Viscosity of Pure Organic Liquids and Binary Liquid Mixtures. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-49218-5_1858.

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