(E)-N′-(5-Bromo-2-methoxy­benzyl­idene)-4-chloro­benzohydrazide

The title Schiff base compound, C(15)H(12)BrClN(2)O(2), crystallizes with two independent mol­ecules in the asymmetric unit. The mol­ecules adopt an E configuration with respect to the C=N double bond. The dihedral angles between the benzene rings are 24.4 (2) and 9.4 (2)° in the two mol­ecules. The...

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Autor principal: Lin, Hong-Wei
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2008
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961851/
https://www.ncbi.nlm.nih.gov/pubmed/21202907
http://dx.doi.org/10.1107/S1600536808017911
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author Lin, Hong-Wei
author_facet Lin, Hong-Wei
author_sort Lin, Hong-Wei
collection PubMed
description The title Schiff base compound, C(15)H(12)BrClN(2)O(2), crystallizes with two independent mol­ecules in the asymmetric unit. The mol­ecules adopt an E configuration with respect to the C=N double bond. The dihedral angles between the benzene rings are 24.4 (2) and 9.4 (2)° in the two mol­ecules. The crystal structure is stabilized by inter­molecular N—H⋯O hydrogen bonds, forming chains running along the b axis.
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spelling pubmed-29618512010-12-30 (E)-N′-(5-Bromo-2-methoxy­benzyl­idene)-4-chloro­benzohydrazide Lin, Hong-Wei Acta Crystallogr Sect E Struct Rep Online Organic Papers The title Schiff base compound, C(15)H(12)BrClN(2)O(2), crystallizes with two independent mol­ecules in the asymmetric unit. The mol­ecules adopt an E configuration with respect to the C=N double bond. The dihedral angles between the benzene rings are 24.4 (2) and 9.4 (2)° in the two mol­ecules. The crystal structure is stabilized by inter­molecular N—H⋯O hydrogen bonds, forming chains running along the b axis. International Union of Crystallography 2008-06-19 /pmc/articles/PMC2961851/ /pubmed/21202907 http://dx.doi.org/10.1107/S1600536808017911 Text en © Hong-Wei Lin 2008 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
Lin, Hong-Wei
(E)-N′-(5-Bromo-2-methoxy­benzyl­idene)-4-chloro­benzohydrazide
title (E)-N′-(5-Bromo-2-methoxy­benzyl­idene)-4-chloro­benzohydrazide
title_full (E)-N′-(5-Bromo-2-methoxy­benzyl­idene)-4-chloro­benzohydrazide
title_fullStr (E)-N′-(5-Bromo-2-methoxy­benzyl­idene)-4-chloro­benzohydrazide
title_full_unstemmed (E)-N′-(5-Bromo-2-methoxy­benzyl­idene)-4-chloro­benzohydrazide
title_short (E)-N′-(5-Bromo-2-methoxy­benzyl­idene)-4-chloro­benzohydrazide
title_sort (e)-n′-(5-bromo-2-methoxy­benzyl­idene)-4-chloro­benzohydrazide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961851/
https://www.ncbi.nlm.nih.gov/pubmed/21202907
http://dx.doi.org/10.1107/S1600536808017911
work_keys_str_mv AT linhongwei en5bromo2methoxybenzylidene4chlorobenzohydrazide

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