(E)-4-Amino-N′-(5-bromo-2-hy­droxy­benzyl­idene)benzohydrazide mono­hydrate

In t the title compound, C(14)H(12)BrN(3)O(2). H(2)O, the conformation of the C=N double bond in the hydrazide Schiff base mol­ecule is E. The dihedral angle between the benzene rings is 48.01 (11) °. An intra­molecular O—H⋯N hydrogen bond makes an S(6) ring motif. In the crystal, mol­ecules are lin...

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Detalles Bibliográficos
Autores principales: Kargar, Hadi, Kia, Reza, Tahir, Muhammad Nawaz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3393931/
https://www.ncbi.nlm.nih.gov/pubmed/22798796
http://dx.doi.org/10.1107/S1600536812025950
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author Kargar, Hadi
Kia, Reza
Tahir, Muhammad Nawaz
author_facet Kargar, Hadi
Kia, Reza
Tahir, Muhammad Nawaz
author_sort Kargar, Hadi
collection PubMed
description In t the title compound, C(14)H(12)BrN(3)O(2). H(2)O, the conformation of the C=N double bond in the hydrazide Schiff base mol­ecule is E. The dihedral angle between the benzene rings is 48.01 (11) °. An intra­molecular O—H⋯N hydrogen bond makes an S(6) ring motif. In the crystal, mol­ecules are linked through N—H⋯O (bifurcated acceptor) and O—H⋯O hydrogen bonds, forming two-dimensional networks lying parallel to (100).
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spelling pubmed-33939312012-07-13 (E)-4-Amino-N′-(5-bromo-2-hy­droxy­benzyl­idene)benzohydrazide mono­hydrate Kargar, Hadi Kia, Reza Tahir, Muhammad Nawaz Acta Crystallogr Sect E Struct Rep Online Organic Papers In t the title compound, C(14)H(12)BrN(3)O(2). H(2)O, the conformation of the C=N double bond in the hydrazide Schiff base mol­ecule is E. The dihedral angle between the benzene rings is 48.01 (11) °. An intra­molecular O—H⋯N hydrogen bond makes an S(6) ring motif. In the crystal, mol­ecules are linked through N—H⋯O (bifurcated acceptor) and O—H⋯O hydrogen bonds, forming two-dimensional networks lying parallel to (100). International Union of Crystallography 2012-06-16 /pmc/articles/PMC3393931/ /pubmed/22798796 http://dx.doi.org/10.1107/S1600536812025950 Text en © Kargar et al. 2012 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
Kargar, Hadi
Kia, Reza
Tahir, Muhammad Nawaz
(E)-4-Amino-N′-(5-bromo-2-hy­droxy­benzyl­idene)benzohydrazide mono­hydrate
title (E)-4-Amino-N′-(5-bromo-2-hy­droxy­benzyl­idene)benzohydrazide mono­hydrate
title_full (E)-4-Amino-N′-(5-bromo-2-hy­droxy­benzyl­idene)benzohydrazide mono­hydrate
title_fullStr (E)-4-Amino-N′-(5-bromo-2-hy­droxy­benzyl­idene)benzohydrazide mono­hydrate
title_full_unstemmed (E)-4-Amino-N′-(5-bromo-2-hy­droxy­benzyl­idene)benzohydrazide mono­hydrate
title_short (E)-4-Amino-N′-(5-bromo-2-hy­droxy­benzyl­idene)benzohydrazide mono­hydrate
title_sort (e)-4-amino-n′-(5-bromo-2-hy­droxy­benzyl­idene)benzohydrazide mono­hydrate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3393931/
https://www.ncbi.nlm.nih.gov/pubmed/22798796
http://dx.doi.org/10.1107/S1600536812025950
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AT tahirmuhammadnawaz e4aminon5bromo2hydroxybenzylidenebenzohydrazidemonohydrate

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