N′-(2-Chloro­benzyl­idene)-2-hydr­oxy-3-methyl­benzohydrazide

In the title compound, C(15)H(13)ClN(2)O(2), the dihedral angle between the two benzene rings is 3.4 (5)° and the mol­ecule adopts an E configuration with respect to the C=N bond. There is an intra­molecular O—H⋯O hydrogen bond in the mol­ecule, which generates an S(6) loop. In the crystal structure...

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Detalles Bibliográficos
Autores principales: Han, You-Yue, Zhao, Qiu-Rong
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979247/
https://www.ncbi.nlm.nih.gov/pubmed/21579089
http://dx.doi.org/10.1107/S1600536810012110
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author Han, You-Yue
Zhao, Qiu-Rong
author_facet Han, You-Yue
Zhao, Qiu-Rong
author_sort Han, You-Yue
collection PubMed
description In the title compound, C(15)H(13)ClN(2)O(2), the dihedral angle between the two benzene rings is 3.4 (5)° and the mol­ecule adopts an E configuration with respect to the C=N bond. There is an intra­molecular O—H⋯O hydrogen bond in the mol­ecule, which generates an S(6) loop. In the crystal structure, mol­ecules are linked through inter­molecular N—H⋯O hydrogen bonds, forming C(4) chains running along the a axis.
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spelling pubmed-29792472010-12-30 N′-(2-Chloro­benzyl­idene)-2-hydr­oxy-3-methyl­benzohydrazide Han, You-Yue Zhao, Qiu-Rong Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(15)H(13)ClN(2)O(2), the dihedral angle between the two benzene rings is 3.4 (5)° and the mol­ecule adopts an E configuration with respect to the C=N bond. There is an intra­molecular O—H⋯O hydrogen bond in the mol­ecule, which generates an S(6) loop. In the crystal structure, mol­ecules are linked through inter­molecular N—H⋯O hydrogen bonds, forming C(4) chains running along the a axis. International Union of Crystallography 2010-04-02 /pmc/articles/PMC2979247/ /pubmed/21579089 http://dx.doi.org/10.1107/S1600536810012110 Text en © Han and Zhao 2010 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
Han, You-Yue
Zhao, Qiu-Rong
N′-(2-Chloro­benzyl­idene)-2-hydr­oxy-3-methyl­benzohydrazide
title N′-(2-Chloro­benzyl­idene)-2-hydr­oxy-3-methyl­benzohydrazide
title_full N′-(2-Chloro­benzyl­idene)-2-hydr­oxy-3-methyl­benzohydrazide
title_fullStr N′-(2-Chloro­benzyl­idene)-2-hydr­oxy-3-methyl­benzohydrazide
title_full_unstemmed N′-(2-Chloro­benzyl­idene)-2-hydr­oxy-3-methyl­benzohydrazide
title_short N′-(2-Chloro­benzyl­idene)-2-hydr­oxy-3-methyl­benzohydrazide
title_sort n′-(2-chloro­benzyl­idene)-2-hydr­oxy-3-methyl­benzohydrazide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979247/
https://www.ncbi.nlm.nih.gov/pubmed/21579089
http://dx.doi.org/10.1107/S1600536810012110
work_keys_str_mv AT hanyouyue n2chlorobenzylidene2hydroxy3methylbenzohydrazide
AT zhaoqiurong n2chlorobenzylidene2hydroxy3methylbenzohydrazide

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