(E)-3-Bromo-N′-(2-chloro­benzyl­idene)benzohydrazide

The title compound, C(14)H(10)BrClN(2)O, was synthesized by the reaction of 2-chloro­benzaldehyde with an equimolar quantity of 3-bromo­benzohydrazide in methanol. The mol­ecule displays an E configuration about the C=N bond. The dihedral angle between the two benzene rings is 13.0 (2)°. In the crys...

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Detalles Bibliográficos
Autores principales: Qu, Lan-Zhu, Cao, Guo-Biao
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969211/
https://www.ncbi.nlm.nih.gov/pubmed/21582957
http://dx.doi.org/10.1107/S160053680902412X
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author Qu, Lan-Zhu
Cao, Guo-Biao
author_facet Qu, Lan-Zhu
Cao, Guo-Biao
author_sort Qu, Lan-Zhu
collection PubMed
description The title compound, C(14)H(10)BrClN(2)O, was synthesized by the reaction of 2-chloro­benzaldehyde with an equimolar quantity of 3-bromo­benzohydrazide in methanol. The mol­ecule displays an E configuration about the C=N bond. The dihedral angle between the two benzene rings is 13.0 (2)°. In the crystal structure, mol­ecules are linked through inter­molecular N—H⋯O hydrogen bonds, forming chains propagating along the c axis.
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spelling pubmed-29692112010-12-30 (E)-3-Bromo-N′-(2-chloro­benzyl­idene)benzohydrazide Qu, Lan-Zhu Cao, Guo-Biao Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(14)H(10)BrClN(2)O, was synthesized by the reaction of 2-chloro­benzaldehyde with an equimolar quantity of 3-bromo­benzohydrazide in methanol. The mol­ecule displays an E configuration about the C=N bond. The dihedral angle between the two benzene rings is 13.0 (2)°. In the crystal structure, mol­ecules are linked through inter­molecular N—H⋯O hydrogen bonds, forming chains propagating along the c axis. International Union of Crystallography 2009-06-27 /pmc/articles/PMC2969211/ /pubmed/21582957 http://dx.doi.org/10.1107/S160053680902412X Text en © Qu and Cao 2009 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
Qu, Lan-Zhu
Cao, Guo-Biao
(E)-3-Bromo-N′-(2-chloro­benzyl­idene)benzohydrazide
title (E)-3-Bromo-N′-(2-chloro­benzyl­idene)benzohydrazide
title_full (E)-3-Bromo-N′-(2-chloro­benzyl­idene)benzohydrazide
title_fullStr (E)-3-Bromo-N′-(2-chloro­benzyl­idene)benzohydrazide
title_full_unstemmed (E)-3-Bromo-N′-(2-chloro­benzyl­idene)benzohydrazide
title_short (E)-3-Bromo-N′-(2-chloro­benzyl­idene)benzohydrazide
title_sort (e)-3-bromo-n′-(2-chloro­benzyl­idene)benzohydrazide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969211/
https://www.ncbi.nlm.nih.gov/pubmed/21582957
http://dx.doi.org/10.1107/S160053680902412X
work_keys_str_mv AT qulanzhu e3bromon2chlorobenzylidenebenzohydrazide
AT caoguobiao e3bromon2chlorobenzylidenebenzohydrazide

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