(E)-N′-(3-Hy­droxy-4-meth­oxy­benzyl­idene)-4-meth­oxy­benzohydrazide

The title mol­ecule, a benzohydrazide derivative, C(16)H(16)N(2)O(4), is twisted with a dihedral angle of 69.97 (5)° between the two benzene rings. An intra­molecular O—H⋯O hydrogen bond generates an S(5) ring motif. In the crystal, mol­ecules are linked by N—H⋯O and weak C—H⋯O hydrogen bonds into a...

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Detalles Bibliográficos
Autores principales: Fun, Hoong-Kun, Promdet, Premrudee, Chantrapromma, Suchada, Horkaew, Jirapa, Karalai, Chatchanok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3239014/
https://www.ncbi.nlm.nih.gov/pubmed/22199863
http://dx.doi.org/10.1107/S1600536811048240
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author Fun, Hoong-Kun
Promdet, Premrudee
Chantrapromma, Suchada
Horkaew, Jirapa
Karalai, Chatchanok
author_facet Fun, Hoong-Kun
Promdet, Premrudee
Chantrapromma, Suchada
Horkaew, Jirapa
Karalai, Chatchanok
author_sort Fun, Hoong-Kun
collection PubMed
description The title mol­ecule, a benzohydrazide derivative, C(16)H(16)N(2)O(4), is twisted with a dihedral angle of 69.97 (5)° between the two benzene rings. An intra­molecular O—H⋯O hydrogen bond generates an S(5) ring motif. In the crystal, mol­ecules are linked by N—H⋯O and weak C—H⋯O hydrogen bonds into a chain along the c axis. C—H⋯π inter­actions are also present.
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spelling pubmed-32390142011-12-23 (E)-N′-(3-Hy­droxy-4-meth­oxy­benzyl­idene)-4-meth­oxy­benzohydrazide Fun, Hoong-Kun Promdet, Premrudee Chantrapromma, Suchada Horkaew, Jirapa Karalai, Chatchanok Acta Crystallogr Sect E Struct Rep Online Organic Papers The title mol­ecule, a benzohydrazide derivative, C(16)H(16)N(2)O(4), is twisted with a dihedral angle of 69.97 (5)° between the two benzene rings. An intra­molecular O—H⋯O hydrogen bond generates an S(5) ring motif. In the crystal, mol­ecules are linked by N—H⋯O and weak C—H⋯O hydrogen bonds into a chain along the c axis. C—H⋯π inter­actions are also present. International Union of Crystallography 2011-11-19 /pmc/articles/PMC3239014/ /pubmed/22199863 http://dx.doi.org/10.1107/S1600536811048240 Text en © Fun et al. 2011 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
Fun, Hoong-Kun
Promdet, Premrudee
Chantrapromma, Suchada
Horkaew, Jirapa
Karalai, Chatchanok
(E)-N′-(3-Hy­droxy-4-meth­oxy­benzyl­idene)-4-meth­oxy­benzohydrazide
title (E)-N′-(3-Hy­droxy-4-meth­oxy­benzyl­idene)-4-meth­oxy­benzohydrazide
title_full (E)-N′-(3-Hy­droxy-4-meth­oxy­benzyl­idene)-4-meth­oxy­benzohydrazide
title_fullStr (E)-N′-(3-Hy­droxy-4-meth­oxy­benzyl­idene)-4-meth­oxy­benzohydrazide
title_full_unstemmed (E)-N′-(3-Hy­droxy-4-meth­oxy­benzyl­idene)-4-meth­oxy­benzohydrazide
title_short (E)-N′-(3-Hy­droxy-4-meth­oxy­benzyl­idene)-4-meth­oxy­benzohydrazide
title_sort (e)-n′-(3-hy­droxy-4-meth­oxy­benzyl­idene)-4-meth­oxy­benzohydrazide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3239014/
https://www.ncbi.nlm.nih.gov/pubmed/22199863
http://dx.doi.org/10.1107/S1600536811048240
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