Relevant bibliographies by topics / 3-hydroxybenzaldehyde

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  3. Conference papers

Academic literature on the topic '3-hydroxybenzaldehyde'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "3-hydroxybenzaldehyde"

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Li, Jing, Suan Shi, Sushil Adhikari, and Maobing Tu. "Inhibition effect of aromatic aldehydes on butanol fermentation by Clostridium acetobutylicum." RSC Advances 7, no. 3 (2017): 1241–50. http://dx.doi.org/10.1039/c6ra25706b.

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Paixão, J. A., A. Matos Beja, M. Ramos Silva, L. Alte da Veiga, and A. C. Serra. "3-Hydroxybenzaldehyde." Acta Crystallographica Section C Crystal Structure Communications 56, no. 11 (2000): 1348–50. http://dx.doi.org/10.1107/s0108270100010441.

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Li, Yong, Xinxi Zhang, Jun Zheng, and Xiaoling Wang. "3-Ethoxy-4-hydroxybenzaldehyde." Acta Crystallographica Section E Structure Reports Online 64, no. 10 (2008): o2008. http://dx.doi.org/10.1107/s1600536808030419.

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Metlay, Jessica B., and Joseph M. Tanski. "3-Bromo-2-hydroxybenzaldehyde." Acta Crystallographica Section E Structure Reports Online 68, no. 8 (2012): o2484. http://dx.doi.org/10.1107/s1600536812031510.

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The molecule of the title compound, C7H5BrO2, is almost planar (r.m.s. deviation from the plane of all the non-H atoms = 0.0271 Å) and displays intramolecular O—H...O hydrogen bonding between the phenol group and the aldehyde O atom. Packing is directed by weak intermolecular C—H...Br interactions and π-stacking between nearly parallel molecules [dihedral angle = 5.30 (6)° and centroid–centroid distance = 3.752 (1) Å].
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Fu, Wei-Wei. "3-Chloromethyl-2-hydroxybenzaldehyde." Acta Crystallographica Section E Structure Reports Online 68, no. 10 (2012): o2928. http://dx.doi.org/10.1107/s1600536812038421.

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van Otterlo, Willem A. L., Joseph P. Michael, Manuel A. Fernandes, and Charles B. de Koning. "Unforeseen formation of 2-bromo-3-hydroxybenzaldehyde by bromination of 3-hydroxybenzaldehyde." Tetrahedron Letters 45, no. 26 (2004): 5091–94. http://dx.doi.org/10.1016/j.tetlet.2004.04.174.

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Sychyeva, Ye S., and M. S. Mukanova. "SYNTHESIS AND CHEMICAL MODIFICATION OF NEW HYDROXYBEZALDEHYDE DERIVATIVES." Chemical Journal of Kazakhstan, no. 3 (September 15, 2023): 127–36. http://dx.doi.org/10.51580/2023-3.2710-1185.34.

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A high pharmacological ability of aromatic benzaldehydes makes them important intermediates for the synthesis of medicinal preparations, such as anticancer, bactericidal, antifungal, and herbicidal drugs. The purpose of this work is the synthesis of biologically active compounds, based on 4-hydroxybenzaldehyde and 4-hydroxy-3-methoxybenzaldehyde and the establishment of the structure of the synthesized compounds. Results and discussion. New carbonodithioates, based on O-aromatic systems have been synthesized by the interaction of 4-hydroxybenzaldehyde and 4-hydroxy-3-methoxybenzaldehyde with c
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Nowak, Patryk, and Artur Sikorski. "Structural diversity of cocrystals formed from acridine and two isomers of hydroxybenzaldehyde: 3-hydroxybenzaldehyde and 4-hydroxybenzaldehyde." RSC Advances 13, no. 29 (2023): 20105–12. http://dx.doi.org/10.1039/d3ra02300a.

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Based on experiments carried out using SCXRD, FTIR, and TG/DSC methods, it was demonstrated that acridine forms cocrystals with two isomers of hydroxybenzaldehyde: 3-hydroxybenzaldehyde and 4-hydroxybenzaldehyde in a molar ratio of 1 : 1.
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Ribeiro da Silva, Maria D. M. C., Mariana V. Gonçalves, and Manuel J. S. Monte. "Thermodynamic study on hydroxybenzaldehyde derivatives: 3- and 4-Hydroxybenzaldehyde isomers and 3,5-di-tert-butyl-2-hydroxybenzaldehyde." Journal of Chemical Thermodynamics 42, no. 4 (2010): 472–77. http://dx.doi.org/10.1016/j.jct.2009.10.009.

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Tran, Hieu Quang, Hien Cao Nguyen, Thin Van Nguyen, Thanh Thi Nguyen, Toan Ngoc Vo, and Cong Tien Nguyend. "Synthesis and Evaluation of Cytotoxic Activity on Mcf-7 Cell Line of Some Diesters Derived from 5-(Hydroxybenzylidene)Thiazolidine-2,4-Diones." Acta Chemica Iasi 26, no. 2 (2018): 233–48. http://dx.doi.org/10.2478/achi-2018-0015.

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Abstract Knoevenagel condensation of thiazolidine-2,4-dione, which were prepared from chloroacetic acid and thioure by 1,3 dipolar cycloaddition reaction, with 2-hydroxybenzaldehyde, 5-bromo-2-hydroxybenzaldehyde, 3-hydroxybenzaldehyde, 4-hydroxybenzaldehyde and 4-hydoxy-3-methoxybezaldehyde gave five corresponding 5-(hydroxybenzylidene)thiazolidine-2,4-dione compounds. The reaction of 5-(hydroxybenzylidene)thiazolidine-2,4-diones and ethyl chlorofomate or ethyl chloroacetate occurred at both NH and OH centers and gave ten corresponding diesters. The structures of the diesters were confirmed b
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Book chapters on the topic "3-hydroxybenzaldehyde"

1

Hirota, E., K. Kuchitsu, T. Steimle, J. Vogt, and N. Vogt. "182 C9H10O3 3-Ethoxy-4-hydroxybenzaldehyde." In Molecules Containing Three or Four Carbon Atoms and Molecules Containing Five or More Carbon Atoms. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-642-41504-3_313.

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Pardasani, R. T., and P. Pardasani. "Molar magnetic moment of bis{[(2-hydroxybenzaldehyde)-3-isatin]-bishydrazonato}cobalt(II)." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 2. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62466-1_402.

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Pardasani, R. T., and P. Pardasani. "Molar magnetic moment of bis{[(2-hydroxybenzaldehyde)-3-isatin]-bishydrazonato}iron(II)." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 2. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62466-1_14.

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Pardasani, R. T., and P. Pardasani. "Molar magnetic moment of bis{[(2-hydroxybenzaldehyde)-3-isatin]-bishydrazonato}manganese(II)." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 1. Springer Berlin Heidelberg, 2021. http://dx.doi.org/10.1007/978-3-662-62478-4_335.

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Pardasani, R. T., and P. Pardasani. "Magnetic properties of 4,4′-bipyridine bridged binuclear copper(II) complex with thiosemicarbazone of 2-hydroxybenzaldehyde." In Magnetic Properties of Paramagnetic Compounds, Magnetic Susceptibility Data, Volume 6. Springer Berlin Heidelberg, 2022. http://dx.doi.org/10.1007/978-3-662-65056-1_430.

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Conference papers on the topic "3-hydroxybenzaldehyde"

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Arlikatti, Nandini V., Anita R. Shettar, J. Tonannavar, Jayashree Yenagi, V. K. Vaidyan, and V. S. Jayakumar. "Vibrational Assignments and Electronic Structure Calculations for 3-Chloro-4-Hydroxybenzaldehyde." In PERSPECTIVES IN VIBRATIONAL SPECTROSCOPY: Proceedings of the 2nd International Conference on Perspectives in Vibrational Spectroscopy (ICOPVS 2008). AIP, 2008. http://dx.doi.org/10.1063/1.3046233.

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Yuliati, Leny, Tiffany M. D. I. Nazela, and Krisfian T. A. Priyangga. "Detection of triethylamine on supramolecular 3-[(E)-(4- acetylphenyl)diazenyl]-4-hydroxybenzaldehyde compound." In 4TH INTERNATIONAL SEMINAR ON CHEMISTRY. AIP Publishing, 2021. http://dx.doi.org/10.1063/5.0051964.

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