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Relevant bibliographies by topics / 4-chlorobenzaldehyde

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Academic literature on the topic '4-chlorobenzaldehyde'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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Journal articles on the topic "4-chlorobenzaldehyde"

1

Hania, Majed M. "Synthesis and Antibacterial Activity of Some Transition Metal Complexes of Oxime, Semicarbazone and Phenylhydrazone." E-Journal of Chemistry 6, s1 (2009): S508—S514. http://dx.doi.org/10.1155/2009/204714.

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Co, Ni and Cu complexes have been prepared by reacting metal chloride with 4-chlorobenzaldehyde oxime, 4-methylbenzaldehyde oxime, 4-nitrobenzaldehyde oxime, 4-chlorobenzaldehyde semicarbazone, 4-methyl- benzaldehyde semicarbazone, 4-nitrobenzaldehyde semicarbazone, 4-chloro benzaldehyde phenylhydrazone, 4-methylbenzaldehyde phenyl hydrazone and 4-nitrobenzaldehyde phenylhydrazone and their antibacterial activity have been studied and compared with their ligands againstE. coliwhich gave significant results of activity.

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2

Yuan, Cui-Cui, Li Wu, Zhi-Yong Xing, and Xue-Fang Shi. "4-Chlorobenzaldehyde (pyrazin-2-ylcarbonyl)hydrazone." Acta Crystallographica Section E Structure Reports Online 62, no. 8 (2006): o3274—o3275. http://dx.doi.org/10.1107/s1600536806026006.

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3

Bekbölet, Miray, and Nikola Getoff. "Degradation of chlorinated benzaldehydes in aqueous solutions by UV-irradiation." International Journal of Photoenergy 4, no. 4 (2002): 133–39. http://dx.doi.org/10.1155/s1110662x02000156.

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Photoinduced degradation of chlorinated benzaldehydes was investigated using UV light with λ = 253.7 nm in aerated aqueous solutions. Substrate degradation rate as expressed by first order reaction kinetics revealed rate constants, k;7.45×10−3min-1,3.90×10−3min-1and3.90×11−2min-1for 2- chlorobenzaldehyde, 3-chlorobenzaldehyde and 4-chlorobenzaldehyde respectively. The decomposition of the substrates was related to the formation of chloride and formaldehyde by homolytic cleavage processes. initial quantum yields and photochemical “GiPH-values” are reported for the degradation of the substrates.

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4

M., R. Manrao, Kaur Matharu Balbir, K. Gill K., K. Kaul V., and R. Sharma J. "Synthesis and biological potential of nitrones of 4-chlorobenzaldehyde and ethylvanillin." Journal of Indian Chemical Society Vol. 86, May 2009 (2009): 531–34. https://doi.org/10.5281/zenodo.5810309.

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Department of Chemistry, Department of Plant Pathology, Punjab Agricultural University, Ludhiana-141 004, Punjab, India <em>Manuscript received 4 December 2006, revised 3 February 2009, accepted 11 February 2009</em> Nitrones of 4-chlorobenzaldehyde (1a-6a) and ethylvanillin (1b-6b) were synthesized by condensing 4- chlorobenzaldehyde (a) and ethylvanillin (b) with phenylhydroxylamines (1-6) in equimolar ratio. The synthesized nitrones were characterized on the basis of elemental analysis and spectral studies and screened for antifungal potential against six phytopathogenic fungi and nematicid

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5

Eryanti, Yum, Rudi Hendra, Tati Herlina, Adel Zamri, and Unang Supratman. "Synthesis of N-methyl-4-piperidone Curcumin Analogues and Their Cytotoxicity Activity against T47D Cell Lines." Indonesian Journal of Chemistry 18, no. 2 (2018): 362. http://dx.doi.org/10.22146/ijc.24174.

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Three piperidone curcumin analogues (N-methyl-(3E,5E)-3,5-bis-(2-chlorobenzylidene)-4-piperidone (1), N-methyl-(3E,5E)-3,5-bis-(3-bromobenzylidene)-4-piperidone (2) and N-methyl-(3E,5E)-3,5-bis-(4-chlorobenzylidene)-4-piperidone (3)) were synthesized from N-methyl-4-piperidone with halogenbenzaldehyde, 2-chlorobenzaldehyde, 3-bromobenzaldehyde and 4-chlorobenzaldehyde. The Claisen-Schmidt condensation reaction was used in alkali condition with combinatorial. All the compounds showed light yellow needle, light yellow powder, and yellow crystal form with percentage of yield 39, 66, and 40%, resp

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6

Arora, Aayushi, Preeti Oswal, Gyandshwar K. Rao, Sushil Kumar, Ajai K. Singh, and Arun Kumar. "Catalytically active nanosized Pd9Te4 (telluropalladinite) and PdTe (kotulskite) alloys: first precursor-architecture controlled synthesis using palladium complexes of organotellurium compounds as single source precursors." RSC Advances 11, no. 13 (2021): 7214–24. http://dx.doi.org/10.1039/d0ra08732g.

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First precursor-architecture controlled synthesis of Pd<sub>9</sub>Te<sub>4</sub> and PdTe nanostructures that have potential applications in Suzuki coupling of 4-chlorobenzaldehyde and catalytic reduction of 4-nitrophenol.

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7

Saha, Supriyo, Vanshita Gupta, Mazen Almehmadi, Meriem Khedraoui, Samir Chtita, and Vikash Jakhmola. "Synthesis, molecular docking, MD simulation, and In vitro alpha-amylase activity of some new imidazole derivatives." INDIAN JOURNAL OF HETEROCYCLIC CHEMISTRY 35, no. 02 (2025): 325. https://doi.org/10.59467/ijhc.2025.35.325.

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A series of imidazole derivatives (F1-F6) was synthesized in three steps starting from benzaldehyde/4- chlorobenzaldehyde. In the first step, benzaldehyde and 4-chlorobenzaldehyde separately reacted with thiamine hydrochloride and formed benzoin derivatives (1 and 5). Then, benzoin derivatives separately reacted with urea, thiourea, and guanidine hydrochloride to form different substituted imidazole derivatives (2, 6; 3, 7; and 4, 8), respectively. In the last step substituted imidazole derivatives afforded the final products (F1-F6) upon reaction with benzoyl chloride. Then the molecules were

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8

Anoopjit, Singh Kooner, Sharma S., and Sharma Poonam. "Synthesis and microbial activity of acrylamides with heteroatoms." Journal of Indian Chemical Society Vol. 91, Feb 2014 (2014): 293–98. https://doi.org/10.5281/zenodo.5749142.

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Department of Chemistry, Punjab Agricultural University, Ludhiana-141 004, Punjab, India <em>E-mail </em>: ajsingh@live.in Department of Plant Breeding and Genetics, Punjab Agricultural University, Ludhiana-141 004, Punjab, India E-mail : sonita_311@rediffmail.com; poonam_sharma@pau.edu <em>Manuscript received 05 September 2012, revised 11 March 2013, accepted 18 April 2013</em> The modified condensation reaction of benzaldehyde (1a), 2-chlorobenzaldehyde (1c), 3-nitrobenzaldehyde (1b) and 4-chlorobenzaldehyde (1d) with <strong>α</strong>-proton containing acids viz. acetic acid (2a) and

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9

Rabeek, S. Mohamed. "Synthesis, Chracterization, DFT – Mep And In Silico Docking Studies of N,2,6-Tris(4-Chlorophenyl)-4-Oxopiperidine-3-Carboxamide." International Journal of Advance and Applied Research 4, no. 42 (2023): 56–59. https://doi.org/10.5281/zenodo.10547859.

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Abstract:An efficient and environmentally friendly method for the synthesis of N,2,6-tris(4-chlorophenyl)-4-oxopiperidine-3-carboxamide. The compound has been derived by the condensation of 4-chloroacetoacetanilide and 4-chlorobenzaldehyde using ammonium formate. The structure of the synthesized compound was elucidated by spectral studies such as IR, 1 H, 13C-NMR, Elemental analysis, DFT calculations and Molecular docking studies.

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10

Wei, Xing Chuan, Zhi Li Liu, Xi Zheng, and Meng Yue Huo. "Systhesis and Spectroscopic Properties of Curcumin Analogues Combined with Chlorine." Advanced Materials Research 554-556 (July 2012): 1919–24. http://dx.doi.org/10.4028/www.scientific.net/amr.554-556.1919.

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Three curcumin analogues were synthesized from 4-chlorobenzaldehyde and cyclohexanone，cyclopentane and aceton，and their spectroscopic properties were determined. The synthetics had the structural properties such as the target compounds，which showed their particular spectroscopic properties．

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Book chapters on the topic "4-chlorobenzaldehyde"

1

Pardasani, R. T., and P. Pardasani. "Magnetic properties of oxovanadium(IV) complex with Schiff-base derived from 3-methyl-4-amino-5-thiolato-1,2,4-triazole and 2-chlorobenzaldehyde." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_75.

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2

Pardasani, R. T., and P. Pardasani. "Magnetic properties of oxovanadium(IV) complex with Schiff-base derived from 3-ethyl-4-amino-5-thiolato-1,2,4-triazole and 2-chlorobenzaldehyde." In Magnetic Properties of Paramagnetic Compounds. Springer Berlin Heidelberg, 2017. http://dx.doi.org/10.1007/978-3-662-54228-6_76.

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