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(E)-4-Amino-N′-(5-chloro-2-hydroxybenzylidene)benzohydrazide
The title compound, C(14)H(12)ClN(3)O(2), displays an E conformation with respect to the C=N double bond. The dihedral angle between the benzene rings is 41.3 (5)°. The molecular structure is stabilized by an intramolecular O—H⋯N hydrogen bond. In the crystal, N—H⋯O and weak N—H⋯Cl hydrogen bonds...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344646/ https://www.ncbi.nlm.nih.gov/pubmed/22590408 http://dx.doi.org/10.1107/S160053681201803X |
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author | Shi, Zhong-Feng Li, Jia-Ming |
author_facet | Shi, Zhong-Feng Li, Jia-Ming |
author_sort | Shi, Zhong-Feng |
collection | PubMed |
description | The title compound, C(14)H(12)ClN(3)O(2), displays an E conformation with respect to the C=N double bond. The dihedral angle between the benzene rings is 41.3 (5)°. The molecular structure is stabilized by an intramolecular O—H⋯N hydrogen bond. In the crystal, N—H⋯O and weak N—H⋯Cl hydrogen bonds link the molecules into a three-dimensional architecture. In addition, there are weak C—H⋯π stacking interactions. |
format | Online Article Text |
id | pubmed-3344646 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-33446462012-05-15 (E)-4-Amino-N′-(5-chloro-2-hydroxybenzylidene)benzohydrazide Shi, Zhong-Feng Li, Jia-Ming Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(14)H(12)ClN(3)O(2), displays an E conformation with respect to the C=N double bond. The dihedral angle between the benzene rings is 41.3 (5)°. The molecular structure is stabilized by an intramolecular O—H⋯N hydrogen bond. In the crystal, N—H⋯O and weak N—H⋯Cl hydrogen bonds link the molecules into a three-dimensional architecture. In addition, there are weak C—H⋯π stacking interactions. International Union of Crystallography 2012-04-28 /pmc/articles/PMC3344646/ /pubmed/22590408 http://dx.doi.org/10.1107/S160053681201803X Text en © Shi and Li 2012 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 Shi, Zhong-Feng Li, Jia-Ming (E)-4-Amino-N′-(5-chloro-2-hydroxybenzylidene)benzohydrazide |
title | (E)-4-Amino-N′-(5-chloro-2-hydroxybenzylidene)benzohydrazide |
title_full | (E)-4-Amino-N′-(5-chloro-2-hydroxybenzylidene)benzohydrazide |
title_fullStr | (E)-4-Amino-N′-(5-chloro-2-hydroxybenzylidene)benzohydrazide |
title_full_unstemmed | (E)-4-Amino-N′-(5-chloro-2-hydroxybenzylidene)benzohydrazide |
title_short | (E)-4-Amino-N′-(5-chloro-2-hydroxybenzylidene)benzohydrazide |
title_sort | (e)-4-amino-n′-(5-chloro-2-hydroxybenzylidene)benzohydrazide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3344646/ https://www.ncbi.nlm.nih.gov/pubmed/22590408 http://dx.doi.org/10.1107/S160053681201803X |
work_keys_str_mv | AT shizhongfeng e4aminon5chloro2hydroxybenzylidenebenzohydrazide AT lijiaming e4aminon5chloro2hydroxybenzylidenebenzohydrazide |