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N′-[(E)-3-Bromo-5-chloro-2-hy­droxy­benzyl­idene]furan-2-carbohydrazide

In the title compound, C(12)H(8)BrClN(2)O(3), the furan ring makes a dihedral angle of 17.2 (2)° with the six-membered ring. An intra­molecular O–H⋯N hydrogen bond stabilizes the mol­ecular conformation. In the crystal, N–H⋯O hydrogen bonds connect the mol­ecules into chains running along the c-axis...

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Detalles Bibliográficos
Autores principales: Sundar, A., Ranjith, S., Rajagopal, G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051112/
https://www.ncbi.nlm.nih.gov/pubmed/24940251
http://dx.doi.org/10.1107/S160053681401085X
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author Sundar, A.
Ranjith, S.
Rajagopal, G.
author_facet Sundar, A.
Ranjith, S.
Rajagopal, G.
author_sort Sundar, A.
collection PubMed
description In the title compound, C(12)H(8)BrClN(2)O(3), the furan ring makes a dihedral angle of 17.2 (2)° with the six-membered ring. An intra­molecular O–H⋯N hydrogen bond stabilizes the mol­ecular conformation. In the crystal, N–H⋯O hydrogen bonds connect the mol­ecules into chains running along the c-axis direction. The crystal packing is additionally stabilized by C—H⋯O inter­actions into a three-dimensional supramolecular architecture.
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spelling pubmed-40511122014-06-17 N′-[(E)-3-Bromo-5-chloro-2-hy­droxy­benzyl­idene]furan-2-carbohydrazide Sundar, A. Ranjith, S. Rajagopal, G. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(12)H(8)BrClN(2)O(3), the furan ring makes a dihedral angle of 17.2 (2)° with the six-membered ring. An intra­molecular O–H⋯N hydrogen bond stabilizes the mol­ecular conformation. In the crystal, N–H⋯O hydrogen bonds connect the mol­ecules into chains running along the c-axis direction. The crystal packing is additionally stabilized by C—H⋯O inter­actions into a three-dimensional supramolecular architecture. International Union of Crystallography 2014-05-17 /pmc/articles/PMC4051112/ /pubmed/24940251 http://dx.doi.org/10.1107/S160053681401085X Text en © Sundar et al. 2014 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
Sundar, A.
Ranjith, S.
Rajagopal, G.
N′-[(E)-3-Bromo-5-chloro-2-hy­droxy­benzyl­idene]furan-2-carbohydrazide
title N′-[(E)-3-Bromo-5-chloro-2-hy­droxy­benzyl­idene]furan-2-carbohydrazide
title_full N′-[(E)-3-Bromo-5-chloro-2-hy­droxy­benzyl­idene]furan-2-carbohydrazide
title_fullStr N′-[(E)-3-Bromo-5-chloro-2-hy­droxy­benzyl­idene]furan-2-carbohydrazide
title_full_unstemmed N′-[(E)-3-Bromo-5-chloro-2-hy­droxy­benzyl­idene]furan-2-carbohydrazide
title_short N′-[(E)-3-Bromo-5-chloro-2-hy­droxy­benzyl­idene]furan-2-carbohydrazide
title_sort n′-[(e)-3-bromo-5-chloro-2-hy­droxy­benzyl­idene]furan-2-carbohydrazide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4051112/
https://www.ncbi.nlm.nih.gov/pubmed/24940251
http://dx.doi.org/10.1107/S160053681401085X
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