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3-Bromo-N′-[(E)-4-hydroxybenzylidene]benzohydrazide
The title compound, C(14)H(11)BrN(2)O(2), was synthesized by the reaction of 4-hydroxybenzaldehyde with an equimolar quantity of 3-bromobenzohydrazide in methanol. The dihedral angle between the two benzene rings is 40.1 (2)°. In the crystal structure, molecules are linked through intermolecular...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961897/ https://www.ncbi.nlm.nih.gov/pubmed/21202828 http://dx.doi.org/10.1107/S1600536808015912 |
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author | Yang, Tao Cao, Guo-Biao Xiang, Ji-Ming Zhang, Li-Hui |
author_facet | Yang, Tao Cao, Guo-Biao Xiang, Ji-Ming Zhang, Li-Hui |
author_sort | Yang, Tao |
collection | PubMed |
description | The title compound, C(14)H(11)BrN(2)O(2), was synthesized by the reaction of 4-hydroxybenzaldehyde with an equimolar quantity of 3-bromobenzohydrazide in methanol. The dihedral angle between the two benzene rings is 40.1 (2)°. In the crystal structure, molecules are linked through intermolecular O—H⋯O, O—H⋯N and N—H⋯O hydrogen bonds to form a three-dimensional network. |
format | Text |
id | pubmed-2961897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29618972010-12-30 3-Bromo-N′-[(E)-4-hydroxybenzylidene]benzohydrazide Yang, Tao Cao, Guo-Biao Xiang, Ji-Ming Zhang, Li-Hui Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(14)H(11)BrN(2)O(2), was synthesized by the reaction of 4-hydroxybenzaldehyde with an equimolar quantity of 3-bromobenzohydrazide in methanol. The dihedral angle between the two benzene rings is 40.1 (2)°. In the crystal structure, molecules are linked through intermolecular O—H⋯O, O—H⋯N and N—H⋯O hydrogen bonds to form a three-dimensional network. International Union of Crystallography 2008-06-07 /pmc/articles/PMC2961897/ /pubmed/21202828 http://dx.doi.org/10.1107/S1600536808015912 Text en © Yang et al. 2008 http://creativecommons.org/licenses/by/2.0/uk/ This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited. |
spellingShingle | Organic Papers Yang, Tao Cao, Guo-Biao Xiang, Ji-Ming Zhang, Li-Hui 3-Bromo-N′-[(E)-4-hydroxybenzylidene]benzohydrazide |
title | 3-Bromo-N′-[(E)-4-hydroxybenzylidene]benzohydrazide |
title_full | 3-Bromo-N′-[(E)-4-hydroxybenzylidene]benzohydrazide |
title_fullStr | 3-Bromo-N′-[(E)-4-hydroxybenzylidene]benzohydrazide |
title_full_unstemmed | 3-Bromo-N′-[(E)-4-hydroxybenzylidene]benzohydrazide |
title_short | 3-Bromo-N′-[(E)-4-hydroxybenzylidene]benzohydrazide |
title_sort | 3-bromo-n′-[(e)-4-hydroxybenzylidene]benzohydrazide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961897/ https://www.ncbi.nlm.nih.gov/pubmed/21202828 http://dx.doi.org/10.1107/S1600536808015912 |
work_keys_str_mv | AT yangtao 3bromone4hydroxybenzylidenebenzohydrazide AT caoguobiao 3bromone4hydroxybenzylidenebenzohydrazide AT xiangjiming 3bromone4hydroxybenzylidenebenzohydrazide AT zhanglihui 3bromone4hydroxybenzylidenebenzohydrazide |