(E)-4-Hy­droxy-N′-(4-hy­droxy-3-meth­oxy­benzyl­idene)benzohydrazide

In the title compound, C(15)H(14)N(2)O(4), the N=C double bond has an E configuration. The two benzene rings make a dihedral angle of 28.59 (6)°. In the crystal, mol­ecules are linked into a three-dimensional network by inter­molecular N—H⋯O, O—H⋯O and C—H⋯O hydrogen bonds and stabilized by weak C—H...

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Detalles Bibliográficos
Autores principales: Shalash, Marwan, Salhin, Abdussalam, Adnan, Rohana, Yeap, Chin Sing, Fun, Hoong-Kun
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3011781/
https://www.ncbi.nlm.nih.gov/pubmed/21589430
http://dx.doi.org/10.1107/S1600536810045162
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author Shalash, Marwan
Salhin, Abdussalam
Adnan, Rohana
Yeap, Chin Sing
Fun, Hoong-Kun
author_facet Shalash, Marwan
Salhin, Abdussalam
Adnan, Rohana
Yeap, Chin Sing
Fun, Hoong-Kun
author_sort Shalash, Marwan
collection PubMed
description In the title compound, C(15)H(14)N(2)O(4), the N=C double bond has an E configuration. The two benzene rings make a dihedral angle of 28.59 (6)°. In the crystal, mol­ecules are linked into a three-dimensional network by inter­molecular N—H⋯O, O—H⋯O and C—H⋯O hydrogen bonds and stabilized by weak C—H⋯π inter­actions.
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spelling pubmed-30117812010-12-30 (E)-4-Hy­droxy-N′-(4-hy­droxy-3-meth­oxy­benzyl­idene)benzohydrazide Shalash, Marwan Salhin, Abdussalam Adnan, Rohana Yeap, Chin Sing Fun, Hoong-Kun Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(15)H(14)N(2)O(4), the N=C double bond has an E configuration. The two benzene rings make a dihedral angle of 28.59 (6)°. In the crystal, mol­ecules are linked into a three-dimensional network by inter­molecular N—H⋯O, O—H⋯O and C—H⋯O hydrogen bonds and stabilized by weak C—H⋯π inter­actions. International Union of Crystallography 2010-11-13 /pmc/articles/PMC3011781/ /pubmed/21589430 http://dx.doi.org/10.1107/S1600536810045162 Text en © Shalash et al. 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
Shalash, Marwan
Salhin, Abdussalam
Adnan, Rohana
Yeap, Chin Sing
Fun, Hoong-Kun
(E)-4-Hy­droxy-N′-(4-hy­droxy-3-meth­oxy­benzyl­idene)benzohydrazide
title (E)-4-Hy­droxy-N′-(4-hy­droxy-3-meth­oxy­benzyl­idene)benzohydrazide
title_full (E)-4-Hy­droxy-N′-(4-hy­droxy-3-meth­oxy­benzyl­idene)benzohydrazide
title_fullStr (E)-4-Hy­droxy-N′-(4-hy­droxy-3-meth­oxy­benzyl­idene)benzohydrazide
title_full_unstemmed (E)-4-Hy­droxy-N′-(4-hy­droxy-3-meth­oxy­benzyl­idene)benzohydrazide
title_short (E)-4-Hy­droxy-N′-(4-hy­droxy-3-meth­oxy­benzyl­idene)benzohydrazide
title_sort (e)-4-hy­droxy-n′-(4-hy­droxy-3-meth­oxy­benzyl­idene)benzohydrazide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3011781/
https://www.ncbi.nlm.nih.gov/pubmed/21589430
http://dx.doi.org/10.1107/S1600536810045162
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