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(E)-2-Meth­oxy-N′-(2,4,6-trihy­droxy­benzyl­idene)benzohydrazide

In the title hydrazone derivative, C(15)H(14)N(2)O(5), the benzene rings are twisted by 7.55 (8)° with respect to each other. The azomethine double bond adopts an E conformation. The mol­ecular structure is stabilized by intra­molecular O—H⋯N and N—H⋯O hydrogen bonds, generating S6 ring motifs. In t...

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Autores principales: Taha, Muhammad, Baharudin, M. Syukri, Ismail, Nor Hadiani, Shah, Syed Adnan Ali, Yousuf, Sammer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569804/
https://www.ncbi.nlm.nih.gov/pubmed/23424550
http://dx.doi.org/10.1107/S1600536813001748
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author Taha, Muhammad
Baharudin, M. Syukri
Ismail, Nor Hadiani
Shah, Syed Adnan Ali
Yousuf, Sammer
author_facet Taha, Muhammad
Baharudin, M. Syukri
Ismail, Nor Hadiani
Shah, Syed Adnan Ali
Yousuf, Sammer
author_sort Taha, Muhammad
collection PubMed
description In the title hydrazone derivative, C(15)H(14)N(2)O(5), the benzene rings are twisted by 7.55 (8)° with respect to each other. The azomethine double bond adopts an E conformation. The mol­ecular structure is stabilized by intra­molecular O—H⋯N and N—H⋯O hydrogen bonds, generating S6 ring motifs. In the crystal, mol­ecules are linked into a three-dimensional network by O—H⋯O hydrogen bonds.
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spelling pubmed-35698042013-02-19 (E)-2-Meth­oxy-N′-(2,4,6-trihy­droxy­benzyl­idene)benzohydrazide Taha, Muhammad Baharudin, M. Syukri Ismail, Nor Hadiani Shah, Syed Adnan Ali Yousuf, Sammer Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title hydrazone derivative, C(15)H(14)N(2)O(5), the benzene rings are twisted by 7.55 (8)° with respect to each other. The azomethine double bond adopts an E conformation. The mol­ecular structure is stabilized by intra­molecular O—H⋯N and N—H⋯O hydrogen bonds, generating S6 ring motifs. In the crystal, mol­ecules are linked into a three-dimensional network by O—H⋯O hydrogen bonds. International Union of Crystallography 2013-01-23 /pmc/articles/PMC3569804/ /pubmed/23424550 http://dx.doi.org/10.1107/S1600536813001748 Text en © Taha et al. 2013 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
Taha, Muhammad
Baharudin, M. Syukri
Ismail, Nor Hadiani
Shah, Syed Adnan Ali
Yousuf, Sammer
(E)-2-Meth­oxy-N′-(2,4,6-trihy­droxy­benzyl­idene)benzohydrazide
title (E)-2-Meth­oxy-N′-(2,4,6-trihy­droxy­benzyl­idene)benzohydrazide
title_full (E)-2-Meth­oxy-N′-(2,4,6-trihy­droxy­benzyl­idene)benzohydrazide
title_fullStr (E)-2-Meth­oxy-N′-(2,4,6-trihy­droxy­benzyl­idene)benzohydrazide
title_full_unstemmed (E)-2-Meth­oxy-N′-(2,4,6-trihy­droxy­benzyl­idene)benzohydrazide
title_short (E)-2-Meth­oxy-N′-(2,4,6-trihy­droxy­benzyl­idene)benzohydrazide
title_sort (e)-2-meth­oxy-n′-(2,4,6-trihy­droxy­benzyl­idene)benzohydrazide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3569804/
https://www.ncbi.nlm.nih.gov/pubmed/23424550
http://dx.doi.org/10.1107/S1600536813001748
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