Relevant bibliographies by topics / 2-hydroxybenzaldehyde

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  4. Conference papers

Academic literature on the topic '2-hydroxybenzaldehyde'

Author: Grafiati
Published: 5 June 2025
Last updated: 2 August 2025

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Journal articles on the topic "2-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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Matos Beja, A., J. A. Paixão, M. Ramos Silva, L. Alte da Veiga, A. M. d'A Rocha Gonsalves, and A. C. Serra. "2-Bromo-5-hydroxybenzaldehyde." Acta Crystallographica Section C Crystal Structure Communications 56, no. 3 (2000): 354–55. http://dx.doi.org/10.1107/s0108270199015267.

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Fan, Ying, Wei You, Hui-Fen Qian, Jian-Lan Liu, and Wei Huang. "3,5-Dibromo-2-hydroxybenzaldehyde." Acta Crystallographica Section E Structure Reports Online 64, no. 5 (2008): o799. http://dx.doi.org/10.1107/s1600536808008726.

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Fan, Ying, Wei You, Jian-Lan Liu, Hui-Fen Qian, and Wei Huang. "3,5-Dichloro-2-hydroxybenzaldehyde." Acta Crystallographica Section E Structure Reports Online 64, no. 6 (2008): o1080. http://dx.doi.org/10.1107/s1600536808013901.

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Wu, Ming-Hu, and Wen-Ju Liu. "5,5′-Selenobis(2-hydroxybenzaldehyde)." Acta Crystallographica Section E Structure Reports Online 67, no. 11 (2011): o2983. http://dx.doi.org/10.1107/s1600536811042097.

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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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Kargar, Hadi, Reza Kia, Mehmet Akkurt, and Orhan Büyükgüngör. "5-Bromo-2-hydroxybenzaldehyde thiosemicarbazone." Acta Crystallographica Section E Structure Reports Online 66, no. 11 (2010): o2999. http://dx.doi.org/10.1107/s1600536810043357.

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Kargar, Hadi, Reza Kia, Mehmet Akkurt, and Orhan Büyükgüngör. "5-Chloro-2-hydroxybenzaldehyde thiosemicarbazone." Acta Crystallographica Section E Structure Reports Online 66, no. 11 (2010): o2981. http://dx.doi.org/10.1107/s1600536810043448.

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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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Books on the topic "2-hydroxybenzaldehyde"

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Jäger, Jürgen. (R)-Oxynitrilase katalysierte Cyanhydrinsynthese mit Hydroxybenzaldehyden: Enantioselektive Synthesen pharmakologisch interessanter 2-Amino-1-aryl-alkohole und Amphetamine. 1996.

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Book chapters on the topic "2-hydroxybenzaldehyde"

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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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Nógrádi, M. "Reaction of an Activated Phenol with a 2-Hydroxybenzaldehyde." In Six-Membered Hetarenes with One Chalcogen. Georg Thieme Verlag KG, 2003. http://dx.doi.org/10.1055/sos-sd-014-00168.

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Williams, A. C., and N. Camp. "Reaction of 2-Hydroxybenzaldehyde Imines and Oximes and 2-Hydroxybenzamides with Carbon Suboxide." In Six-Membered Hetarenes with One Chalcogen. Georg Thieme Verlag KG, 2003. http://dx.doi.org/10.1055/sos-sd-014-00321.

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Nógrádi, M. "Reaction of a 2-Hydroxybenzaldehyde (Salicylaldehyde) with a Carbaldehyde, Ketone, or Acetal." In Six-Membered Hetarenes with One Chalcogen. Georg Thieme Verlag KG, 2003. http://dx.doi.org/10.1055/sos-sd-014-00083.

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Nógrádi, M. "Reaction of a 2-Hydroxybenzaldehyde (Salicylaldehyde) with an α-Methylene Carboxylic Acid Derivative." In Six-Membered Hetarenes with One Chalcogen. Georg Thieme Verlag KG, 2003. http://dx.doi.org/10.1055/sos-sd-014-00088.

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Nógrádi, M. "Reaction of a 2-Hydroxybenzaldehyde (Salicylaldehyde) with Aliphatic or Alicyclic α,α′-Bis(methylene) Ketones." In Six-Membered Hetarenes with One Chalcogen. Georg Thieme Verlag KG, 2003. http://dx.doi.org/10.1055/sos-sd-014-00091.

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Dell, C. P. "From 2-Hydroxybenzaldehydes and 2-Hydroxyphenyl Ketones." In Fused Five-Membered Hetarenes with One Heteroatom. Georg Thieme Verlag KG, 2001. http://dx.doi.org/10.1055/sos-sd-010-00016.

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Conference papers on the topic "2-hydroxybenzaldehyde"

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Yusuf, Muhammad, Destria Roza, and Ahmad Kamil Nasution. "Acetalization of 2-Hydroxybenzaldehyde mechanism using halogen acid catalysts based on ab initio methods." In PROCEEDINGS OF THE 3RD INTERNATIONAL SYMPOSIUM ON APPLIED CHEMISTRY 2017. Author(s), 2017. http://dx.doi.org/10.1063/1.5011869.

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Simijonović, Dušica, Edina Avdović, Žiko Milanović, Dejan Milenković, and Zoran Marković. "Green synthesis of chromeno-pyrimidine derivatives – Part I." In 2nd International Conference on Chemo and Bioinformatics. Institute for Information Technologies, University of Kragujevac, 2023. http://dx.doi.org/10.46793/iccbi23.686s.

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Abstract:
Two different chromeno-pyrimidine derivatives were synthetized in the ionic liquid catalyzed reaction of barbituric acid and substituted salicylaldehydes. The product 5-(7-bromo-2,4-dioxo-1,3,4,5-tetrahydro-2H-chromeno[2,3-d]pyrimidin-5-yl)pyrimidine-2,4,6(1H,3H,5H)-tri-one (CP-1) was obtained in the reaction of barbiruric acid and 5-bromo-2-hydroxybenzaldehyde. The second new product 8,9-dihydroxy-2H-chromeno[2,3-d]pyrimidine-2,4(3H)-dione (CP-2) was yielded in the reaction between barbituric acid and 2,3,4-trihydroxybenzaldehyde. These products were isolated in moderate to good yield after 3
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