{2-[(3-Bromo­benzyl­idene)amino]-5-chloro­phen­yl}(phen­yl)methanone

In the title compound, C(20)H(13)BrClNO, the azomethine double bond [C=N = 1.246 (4) Å] adopts an E conformation. The bromo- and chlorophenyl rings are inclined to one another by 13.70 (11)°, and form dihedral angles of 76.68 (10) and 74.24 (7)°, respectively, with the phenyl ring. In the crystal, m...

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Detalles Bibliográficos
Autores principales: Aslam, M., Anis, I., Afza, N., Safder, M., Yousuf, S.
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/PMC3295437/
https://www.ncbi.nlm.nih.gov/pubmed/22412548
http://dx.doi.org/10.1107/S1600536812004667
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author Aslam, M.
Anis, I.
Afza, N.
Safder, M.
Yousuf, S.
author_facet Aslam, M.
Anis, I.
Afza, N.
Safder, M.
Yousuf, S.
author_sort Aslam, M.
collection PubMed
description In the title compound, C(20)H(13)BrClNO, the azomethine double bond [C=N = 1.246 (4) Å] adopts an E conformation. The bromo- and chlorophenyl rings are inclined to one another by 13.70 (11)°, and form dihedral angles of 76.68 (10) and 74.24 (7)°, respectively, with the phenyl ring. In the crystal, mol­ecules are linked by C—H⋯O hydrogen bonds to form double stranded chains propagating along the b-axis direction.
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spelling pubmed-32954372012-03-12 {2-[(3-Bromo­benzyl­idene)amino]-5-chloro­phen­yl}(phen­yl)methanone Aslam, M. Anis, I. Afza, N. Safder, M. Yousuf, S. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(20)H(13)BrClNO, the azomethine double bond [C=N = 1.246 (4) Å] adopts an E conformation. The bromo- and chlorophenyl rings are inclined to one another by 13.70 (11)°, and form dihedral angles of 76.68 (10) and 74.24 (7)°, respectively, with the phenyl ring. In the crystal, mol­ecules are linked by C—H⋯O hydrogen bonds to form double stranded chains propagating along the b-axis direction. International Union of Crystallography 2012-02-10 /pmc/articles/PMC3295437/ /pubmed/22412548 http://dx.doi.org/10.1107/S1600536812004667 Text en © Aslam 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
Aslam, M.
Anis, I.
Afza, N.
Safder, M.
Yousuf, S.
{2-[(3-Bromo­benzyl­idene)amino]-5-chloro­phen­yl}(phen­yl)methanone
title {2-[(3-Bromo­benzyl­idene)amino]-5-chloro­phen­yl}(phen­yl)methanone
title_full {2-[(3-Bromo­benzyl­idene)amino]-5-chloro­phen­yl}(phen­yl)methanone
title_fullStr {2-[(3-Bromo­benzyl­idene)amino]-5-chloro­phen­yl}(phen­yl)methanone
title_full_unstemmed {2-[(3-Bromo­benzyl­idene)amino]-5-chloro­phen­yl}(phen­yl)methanone
title_short {2-[(3-Bromo­benzyl­idene)amino]-5-chloro­phen­yl}(phen­yl)methanone
title_sort {2-[(3-bromo­benzyl­idene)amino]-5-chloro­phen­yl}(phen­yl)methanone
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3295437/
https://www.ncbi.nlm.nih.gov/pubmed/22412548
http://dx.doi.org/10.1107/S1600536812004667
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AT anisi 23bromobenzylideneamino5chlorophenylphenylmethanone
AT afzan 23bromobenzylideneamino5chlorophenylphenylmethanone
AT safderm 23bromobenzylideneamino5chlorophenylphenylmethanone
AT yousufs 23bromobenzylideneamino5chlorophenylphenylmethanone

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