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Journal articles on the topic 'Dimethylacetophenone'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

FAZLUR, RAHMAN, N. RASTOGI S., and K. JETLEY U. "Stability Constants of some Bivalent Metal Complexes with 2-Hydroxy-3,5-dimethylacetophenone Oxime." Journal of Indian Chemical Society Vol. 67, April 1990 (1990): 342. https://doi.org/10.5281/zenodo.6163860.

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Chemical Laboratories, D. N. College, Meerut-250 002 <em>Manuscript received 23 March 1989, revised 15 September 1989, accepted 10 November 1989</em> Stability Constants of some Bivalent Metal Complexes with 2-Hydroxy-3,5-dimethylacetophenone Oxime.

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2

U., K. JETLEY, SINGH JAI, MANU SHUKLA (Ms.), REHMAN FAZLUR, and N. RASTOGI S. "Magnetic and Spectral Studies on the Complexes of 2-Hydroxy-3,5-dimethylacetophenone and its Oxime." Journal Of Indian Chemical Society Vol. 67, Dec 1990 (1990): 987–88. https://doi.org/10.5281/zenodo.6277000.

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Chemical Laboratories, D. N. College, Meerut-250 002  <em>Manuscript received 19 April 1989, revised 4 October 1990, accepted 24 October 1990</em> Magnetic and Spectral Studies on the Complexes of 2-Hydroxy-3,5-dimethylacetophenone and its Oxime

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3

Chattopadhyay, D., T. Banerjee, S. K. Mazumdar, G. Podder, S. Kashino, and M. Haisa. "Structure of 3'-acetamido-2,2-dichloro-4',5'-dimethylacetophenone." Acta Crystallographica Section C Crystal Structure Communications 42, no. 9 (1986): 1201–4. http://dx.doi.org/10.1107/s0108270186092880.

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4

Farzaliyeva, Aynur, Abel Maharramov, and Ibrahim Mamedov. "Some Acetophenone Derivatives as Corrosion Inhibitors for Diesel Fuels." Indonesian Journal of Chemical Research 11, no. 3 (2024): 231–34. http://dx.doi.org/10.30598/ijcr.2024.11-ayn.

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The corrosion inhibition activities 2.4-dimethylasetophenone semicarbazone (1), 2.4-dimethylacetophenone thiosemicarbazone (2), (E)-3-(2-allyloxy)phenyl)-1-(4-hydroxy-2-methylphenyl)prop-2-en-1-one (3), (E,E)-3-(5-bromo-2-hydroxyphenyl)-1-(4-hydroxy-2-methylphenyl)prop-2-en-1-one thiosemicarbazone (4) and 3-hydroxy-3-(2-(2-hydroxy-5-methylphenyl)-2-oxoethyl)indolin-2-one (5) have been studied by weight loss measurements for mild steel-3 specimen in diesel fuel. The corrosion rates of the steel-3 are decreased with the increase of the carbazones, chalcone, indolinone concentrati

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5

K., N. NAIK, and B. NAIK H. "Synthesis of some Chalcones and their Antibacterial Activity." Journal of Indian Chemical Society Vol. 67, Oct. 1990 (1990): 844–45. https://doi.org/10.5281/zenodo.6257380.

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Chemistry Department. South Gujarat University. Surat-395 007 <em>Manuscript received 22 December 1989, revised</em> <em>10 May 1990, accepted 3 July 1990</em> Synthesis of some Chalcones and their Antibacterial Activity

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6

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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7

Allonas, X., F. Morlet-Savary, J. Lalevée, and J. P. Fouassier. "A Photodissociation Reaction: Experimental and Computational Study of 2-Hydroxy-2,2-dimethylacetophenone†." Photochemistry and Photobiology 82, no. 1 (2006): 88. http://dx.doi.org/10.1562/2005-05-20-ra-535.

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8

van Koningsveld, H., J. J. Scheele, and J. C. Jansen. "Structure of 4-tert-butyl-2,6-dimethylacetophenone–iron(III) chloride (1/1)." Acta Crystallographica Section C Crystal Structure Communications 42, no. 1 (1986): 41–43. http://dx.doi.org/10.1107/s010827018609738x.

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9

DSilva, E. D. "Structure Report: (2E)-l-(3,4-dimethylphenyl)-3- (3-methylthiophen-2yl)prop-2-en-1-one." Pearl Multidisciplinary Journal 1, no. 1 (2015): 12–21. https://doi.org/10.5281/zenodo.3611183.

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The compound (2E)-l-(3,4-dimethylphenyl)-3-(3-methylthiophen-2-yl)prop-2-en-l-one was synthesized by the reaction of 3-methylthiophene-2-carbaldehyde with 3,4-dimethylacetophenone. The structure of the synthesized compound was characterized by subjecting it to single crystal X-ray diffraction studies. The compound crystallizes in the monoclinic crystal class with space group P 1 21/c 1. The cell  parameters  are a  = 7.1331(4) Å  b =  28.5501(11) Å,  c =  7.2354(5) Å , &be

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10

van Koningsveld, H., J. J. Scheele, and J. C. Jansen. "Structure of 4-tert-butyl-2,6-dimethylacetophenone and comparison with its FeCl3 complex." Acta Crystallographica Section C Crystal Structure Communications 43, no. 2 (1987): 294–96. http://dx.doi.org/10.1107/s0108270187096070.

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11

Sosnovskikh, V. Ya. "Condensation of nitriles of polyhalogenated carboxylic acids and benzonitrile with 2-hydroxy-4,6-dimethylacetophenone." Russian Chemical Bulletin 47, no. 2 (1998): 354–56. http://dx.doi.org/10.1007/bf02498966.

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12

SOSNOVSKIKH, V. YA. "ChemInform Abstract: Condensation of Nitriles of Polyhalogenated Carboxylic Acids and Benzonitrile with 2-Hydroxy-4,6-dimethylacetophenone." ChemInform 29, no. 22 (2010): no. http://dx.doi.org/10.1002/chin.199822098.

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13

Gagare, Dinkar, Raju Patil, Rama Lokhande, Poonam Dwivedi, and Ajay Deshmukh. "Synthesis and characterization of iron (iii) complexes of some 2-hydroxy-4, 5-dimethylacetophenone substituted hydrazones." International Journal of Advanced Chemistry Research 3, no. 1 (2021): 01–10. http://dx.doi.org/10.33545/26646781.2021.v3.i1a.28.

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14

Api, A. M., D. Belsito, D. Botelho, et al. "RIFM fragrance ingredient safety assessment, 4′-tert-butyl-2′,6′-dimethylacetophenone, CAS Registry Number 2040-10-0." Food and Chemical Toxicology 122 (December 2018): S275—S282. http://dx.doi.org/10.1016/j.fct.2018.08.072.

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15

Sunil, K. Talapatra, Mandal Kabita, Biswas Kallolmay, Mandai Sudipta, and Talapatra Bani. "Cross condensation reactions of ethyl cyanoacetate with some keto methylene compounds: Diastereoselective synthesis of Z-2-( cyanoethoxycarbonyl)methylene-1,2- dihydropyridine and Z-2-(cyanoethoxycarbonyl)methylene-2H-pyran derivatives." Journal of Indian Chemical Society Vol. 76, Nov-Dec 1999 (1999): 733–38. https://doi.org/10.5281/zenodo.5867036.

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Centre of Advanced Studies on Natural Products, Department of Chemistry, University College of Science, University of Calcutta, Calcutta-700 009. India <em>Manuscript received 14 October 1999</em> Previously reported ethyl α:,ԑ-dicyano-β,δ-dimethyl-∆<sup>β,δ_</sup>hexadienoate (2) structure for the minor product of the diethylamine catalyzed condensation reaction between ethyl cyanoacetate and acetylacetone has now been revised as 4,6-dimethyi-Z-2- (cyanoethoxycarbonyl)methylene-1,2-dihydropyridine (3) based on its <sup>1</sup>H NMR, <sup>13</sup>C NMR and mass spec

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16

Chimichi, Stefano, Carlo Dell'Erba, Michelangelo Gruttadauria, et al. "Differential substituent effects in 4-X-acetophenones and 4-X-2,6-dimethylacetophenones: basicity constants (pK BH+ ) and 17O chemical shifts." Journal of the Chemical Society, Perkin Transactions 2, no. 5 (1995): 1021. http://dx.doi.org/10.1039/p29950001021.

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17

Dell'Erba, Carlo, Angelo Mugnoli, Renato Noto, et al. "Substituent effects on the gas-phase basicities of4-x-acetophanes and 4-x-2,6-dimethylacetophenones: a comparison with solution basicities." Tetrahedron 53, no. 2 (1997): 731–38. http://dx.doi.org/10.1016/s0040-4020(96)01015-0.

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18

DELL'ERBA, C., A. MUGNOLI, R. NOTO, et al. "ChemInform Abstract: Substituent Effects on the Gas-Phase Basicities of 4-X-Acetophenones and 4-X-2,6-Dimethylacetophenones: A Comparison with Solution Basicities." ChemInform 28, no. 18 (2010): no. http://dx.doi.org/10.1002/chin.199718029.

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19

Bosch, Eric, and Laura Jeffries. "1-(2-Amino-4,5-dimethylphenyl)ethanone." IUCrData 3, no. 2 (2018). http://dx.doi.org/10.1107/s2414314618003139.

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The molecule of the title compound, C10H13NO, also referred to as 2-amino-4,5-dimethylacetophenone, lies on a crystallographic mirror plane with four molecules in the orthorhombic unit cell and features an intramolecular N—H...O hydrogen bond. In the crystal, the molecules are linked by N—H...O hydrogen bonds, forming ribbons along theaaxis that pack to form sheets lying in the (010) plane.

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20

Gagare, Dinkar, Raju Patil, Rama Lokhande, Poonam Dwivedi, and Ajay Deshmukh. "Synthesis and characterization of (E)-2-(1-hydrazonoethyl)-4,5-dimethylphenol from 2-hydroxy-4,5-dimethylacetophenone." Journal of Chemical Sciences 132, no. 1 (2020). http://dx.doi.org/10.1007/s12039-020-01802-4.

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21

Api, A. M., A. Bartlett, D. Belsito, et al. "Update to RIFM fragrance ingredient safety assessment, 4'-tert-butyl-2',6'-dimethylacetophenone, CAS Registry Number 2040-10-0." Food and Chemical Toxicology, December 2024, 115170. https://doi.org/10.1016/j.fct.2024.115170.

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