N-(2,6-Dichloro­phen­yl)-3-methyl­benzamide

In the mol­ecular structure of the title compound, C(14)H(11)Cl(2)NO, the two aromatic rings form a dihedral angle of 70.9 (1)°. The central amido group –NH—C(=O)– makes a dihedral angle of 26.6 (2)° with the methyl­phenyl ring and 82.5 (1)° with the dichloro­phenyl ring. Inter­molecular N—H⋯O hydro...

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Detalles Bibliográficos
Autores principales: Gowda, B. Thimme, Tokarčík, Miroslav, Kožíšek, Jozef, Rodrigues, Vinola Zeena, Fuess, Hartmut
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971261/
https://www.ncbi.nlm.nih.gov/pubmed/21578312
http://dx.doi.org/10.1107/S1600536809039889
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author Gowda, B. Thimme
Tokarčík, Miroslav
Kožíšek, Jozef
Rodrigues, Vinola Zeena
Fuess, Hartmut
author_facet Gowda, B. Thimme
Tokarčík, Miroslav
Kožíšek, Jozef
Rodrigues, Vinola Zeena
Fuess, Hartmut
author_sort Gowda, B. Thimme
collection PubMed
description In the mol­ecular structure of the title compound, C(14)H(11)Cl(2)NO, the two aromatic rings form a dihedral angle of 70.9 (1)°. The central amido group –NH—C(=O)– makes a dihedral angle of 26.6 (2)° with the methyl­phenyl ring and 82.5 (1)° with the dichloro­phenyl ring. Inter­molecular N—H⋯O hydrogen bonds link the mol­ecules into chains running along the c axis of the crystal.
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spelling pubmed-29712612010-12-30 N-(2,6-Dichloro­phen­yl)-3-methyl­benzamide Gowda, B. Thimme Tokarčík, Miroslav Kožíšek, Jozef Rodrigues, Vinola Zeena Fuess, Hartmut Acta Crystallogr Sect E Struct Rep Online Organic Papers In the mol­ecular structure of the title compound, C(14)H(11)Cl(2)NO, the two aromatic rings form a dihedral angle of 70.9 (1)°. The central amido group –NH—C(=O)– makes a dihedral angle of 26.6 (2)° with the methyl­phenyl ring and 82.5 (1)° with the dichloro­phenyl ring. Inter­molecular N—H⋯O hydrogen bonds link the mol­ecules into chains running along the c axis of the crystal. International Union of Crystallography 2009-10-10 /pmc/articles/PMC2971261/ /pubmed/21578312 http://dx.doi.org/10.1107/S1600536809039889 Text en © Gowda et al. 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
Gowda, B. Thimme
Tokarčík, Miroslav
Kožíšek, Jozef
Rodrigues, Vinola Zeena
Fuess, Hartmut
N-(2,6-Dichloro­phen­yl)-3-methyl­benzamide
title N-(2,6-Dichloro­phen­yl)-3-methyl­benzamide
title_full N-(2,6-Dichloro­phen­yl)-3-methyl­benzamide
title_fullStr N-(2,6-Dichloro­phen­yl)-3-methyl­benzamide
title_full_unstemmed N-(2,6-Dichloro­phen­yl)-3-methyl­benzamide
title_short N-(2,6-Dichloro­phen­yl)-3-methyl­benzamide
title_sort n-(2,6-dichloro­phen­yl)-3-methyl­benzamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2971261/
https://www.ncbi.nlm.nih.gov/pubmed/21578312
http://dx.doi.org/10.1107/S1600536809039889
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AT fuesshartmut n26dichlorophenyl3methylbenzamide

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