Cargando…

(E)-N′-(3-Hy­droxy­benzyl­idene)-3-nitro­benzohydrazide

The title compound, C(14)H(11)N(3)O(4), was prepared by the reaction of 3-nitro­benzohydrazide with 3-hy­droxy­benzalde­hyde. The mol­ecule adopts an E configuration about the C=N bond. The dihedral angle between the two benzene rings is 32.3 (2)°. In the crystal, the mol­ecules are linked through i...

Descripción completa

Detalles Bibliográficos
Autores principales: Mao, Fu-Lin, Dai, Chun-Hua
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3050236/
https://www.ncbi.nlm.nih.gov/pubmed/21522781
http://dx.doi.org/10.1107/S1600536810049482
_version_ 1782199316551565312
author Mao, Fu-Lin
Dai, Chun-Hua
author_facet Mao, Fu-Lin
Dai, Chun-Hua
author_sort Mao, Fu-Lin
collection PubMed
description The title compound, C(14)H(11)N(3)O(4), was prepared by the reaction of 3-nitro­benzohydrazide with 3-hy­droxy­benzalde­hyde. The mol­ecule adopts an E configuration about the C=N bond. The dihedral angle between the two benzene rings is 32.3 (2)°. In the crystal, the mol­ecules are linked through inter­molecular N—H⋯O, O—H⋯N, and O—H⋯O hydrogen bonds, forming chains in the a-axis direction.
format Text
id pubmed-3050236
institution National Center for Biotechnology Information
language English
publishDate 2010
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-30502362011-04-26 (E)-N′-(3-Hy­droxy­benzyl­idene)-3-nitro­benzohydrazide Mao, Fu-Lin Dai, Chun-Hua Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(14)H(11)N(3)O(4), was prepared by the reaction of 3-nitro­benzohydrazide with 3-hy­droxy­benzalde­hyde. The mol­ecule adopts an E configuration about the C=N bond. The dihedral angle between the two benzene rings is 32.3 (2)°. In the crystal, the mol­ecules are linked through inter­molecular N—H⋯O, O—H⋯N, and O—H⋯O hydrogen bonds, forming chains in the a-axis direction. International Union of Crystallography 2010-12-04 /pmc/articles/PMC3050236/ /pubmed/21522781 http://dx.doi.org/10.1107/S1600536810049482 Text en © Mao and Dai 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
Mao, Fu-Lin
Dai, Chun-Hua
(E)-N′-(3-Hy­droxy­benzyl­idene)-3-nitro­benzohydrazide
title (E)-N′-(3-Hy­droxy­benzyl­idene)-3-nitro­benzohydrazide
title_full (E)-N′-(3-Hy­droxy­benzyl­idene)-3-nitro­benzohydrazide
title_fullStr (E)-N′-(3-Hy­droxy­benzyl­idene)-3-nitro­benzohydrazide
title_full_unstemmed (E)-N′-(3-Hy­droxy­benzyl­idene)-3-nitro­benzohydrazide
title_short (E)-N′-(3-Hy­droxy­benzyl­idene)-3-nitro­benzohydrazide
title_sort (e)-n′-(3-hy­droxy­benzyl­idene)-3-nitro­benzohydrazide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3050236/
https://www.ncbi.nlm.nih.gov/pubmed/21522781
http://dx.doi.org/10.1107/S1600536810049482
work_keys_str_mv AT maofulin en3hydroxybenzylidene3nitrobenzohydrazide
AT daichunhua en3hydroxybenzylidene3nitrobenzohydrazide