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4-Chloro-N-(3,5-dimethyl­phen­yl)benzamide

In the mol­ecular structure of the title compound, C(15)H(14)ClNO, the amide group forms dihedral angles of 15.8 (2) and 27.2 (2)°, respectively, with the benzoyl and aniline rings, while the angle between the benzoyl and aniline rings is 11.5 (1)°. The crystal structure is stabilized by N—H⋯O hydro...

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Detalles Bibliográficos
Autores principales: Rodrigues, Vinola Z., Gowda, B. Thimme, Vrábel, Viktor, Kožíšek, Jozef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3297881/
https://www.ncbi.nlm.nih.gov/pubmed/22412684
http://dx.doi.org/10.1107/S1600536812007180
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author Rodrigues, Vinola Z.
Gowda, B. Thimme
Vrábel, Viktor
Kožíšek, Jozef
author_facet Rodrigues, Vinola Z.
Gowda, B. Thimme
Vrábel, Viktor
Kožíšek, Jozef
author_sort Rodrigues, Vinola Z.
collection PubMed
description In the mol­ecular structure of the title compound, C(15)H(14)ClNO, the amide group forms dihedral angles of 15.8 (2) and 27.2 (2)°, respectively, with the benzoyl and aniline rings, while the angle between the benzoyl and aniline rings is 11.5 (1)°. The crystal structure is stabilized by N—H⋯O hydrogen bonds, which give rise to infinite chains running along the c axis.
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spelling pubmed-32978812012-03-12 4-Chloro-N-(3,5-dimethyl­phen­yl)benzamide Rodrigues, Vinola Z. Gowda, B. Thimme Vrábel, Viktor Kožíšek, Jozef Acta Crystallogr Sect E Struct Rep Online Organic Papers In the mol­ecular structure of the title compound, C(15)H(14)ClNO, the amide group forms dihedral angles of 15.8 (2) and 27.2 (2)°, respectively, with the benzoyl and aniline rings, while the angle between the benzoyl and aniline rings is 11.5 (1)°. The crystal structure is stabilized by N—H⋯O hydrogen bonds, which give rise to infinite chains running along the c axis. International Union of Crystallography 2012-02-24 /pmc/articles/PMC3297881/ /pubmed/22412684 http://dx.doi.org/10.1107/S1600536812007180 Text en © Rodrigues 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
Rodrigues, Vinola Z.
Gowda, B. Thimme
Vrábel, Viktor
Kožíšek, Jozef
4-Chloro-N-(3,5-dimethyl­phen­yl)benzamide
title 4-Chloro-N-(3,5-dimethyl­phen­yl)benzamide
title_full 4-Chloro-N-(3,5-dimethyl­phen­yl)benzamide
title_fullStr 4-Chloro-N-(3,5-dimethyl­phen­yl)benzamide
title_full_unstemmed 4-Chloro-N-(3,5-dimethyl­phen­yl)benzamide
title_short 4-Chloro-N-(3,5-dimethyl­phen­yl)benzamide
title_sort 4-chloro-n-(3,5-dimethyl­phen­yl)benzamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3297881/
https://www.ncbi.nlm.nih.gov/pubmed/22412684
http://dx.doi.org/10.1107/S1600536812007180
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