(E)-N′-(5-Bromo-2-hy­droxy-3-meth­oxy­benzyl­idene)-1H-indole-3-carbo­hydrazide

There are three independent mol­eculesi n the asymmetric unit of the title compound, C(18)H(16)BrN(3)O(3), in which the dihedral angles between the indole and benzene rings are 76.9 (2), 4.9 (2), and 70.9 (2)°. All three mol­ecules exist in a trans configuration with respect to the methyl­idene unit...

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Autor principal: Li, Xiao-Yan
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/PMC3201537/
https://www.ncbi.nlm.nih.gov/pubmed/22065413
http://dx.doi.org/10.1107/S1600536811039195
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author Li, Xiao-Yan
author_facet Li, Xiao-Yan
author_sort Li, Xiao-Yan
collection PubMed
description There are three independent mol­eculesi n the asymmetric unit of the title compound, C(18)H(16)BrN(3)O(3), in which the dihedral angles between the indole and benzene rings are 76.9 (2), 4.9 (2), and 70.9 (2)°. All three mol­ecules exist in a trans configuration with respect to the methyl­idene units. In each mol­ecule, there is one intra­molecular O—H⋯N hydrogen bond. In the crystal, N—H⋯O hydrogen bonds occur.
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spelling pubmed-32015372011-11-06 (E)-N′-(5-Bromo-2-hy­droxy-3-meth­oxy­benzyl­idene)-1H-indole-3-carbo­hydrazide Li, Xiao-Yan Acta Crystallogr Sect E Struct Rep Online Organic Papers There are three independent mol­eculesi n the asymmetric unit of the title compound, C(18)H(16)BrN(3)O(3), in which the dihedral angles between the indole and benzene rings are 76.9 (2), 4.9 (2), and 70.9 (2)°. All three mol­ecules exist in a trans configuration with respect to the methyl­idene units. In each mol­ecule, there is one intra­molecular O—H⋯N hydrogen bond. In the crystal, N—H⋯O hydrogen bonds occur. International Union of Crystallography 2011-09-30 /pmc/articles/PMC3201537/ /pubmed/22065413 http://dx.doi.org/10.1107/S1600536811039195 Text en © Xiao-Yan Li 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
Li, Xiao-Yan
(E)-N′-(5-Bromo-2-hy­droxy-3-meth­oxy­benzyl­idene)-1H-indole-3-carbo­hydrazide
title (E)-N′-(5-Bromo-2-hy­droxy-3-meth­oxy­benzyl­idene)-1H-indole-3-carbo­hydrazide
title_full (E)-N′-(5-Bromo-2-hy­droxy-3-meth­oxy­benzyl­idene)-1H-indole-3-carbo­hydrazide
title_fullStr (E)-N′-(5-Bromo-2-hy­droxy-3-meth­oxy­benzyl­idene)-1H-indole-3-carbo­hydrazide
title_full_unstemmed (E)-N′-(5-Bromo-2-hy­droxy-3-meth­oxy­benzyl­idene)-1H-indole-3-carbo­hydrazide
title_short (E)-N′-(5-Bromo-2-hy­droxy-3-meth­oxy­benzyl­idene)-1H-indole-3-carbo­hydrazide
title_sort (e)-n′-(5-bromo-2-hy­droxy-3-meth­oxy­benzyl­idene)-1h-indole-3-carbo­hydrazide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3201537/
https://www.ncbi.nlm.nih.gov/pubmed/22065413
http://dx.doi.org/10.1107/S1600536811039195
work_keys_str_mv AT lixiaoyan en5bromo2hydroxy3methoxybenzylidene1hindole3carbohydrazide

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