4-Chloro-N-(2,5-dimethyl­phen­yl)-2-methyl­benzene­sulfonamide

The asymmetric unit of the title compound, C(15)H(16)ClNO(2)S, contains three independent moleules. The conformation of the N—H bonds are anti to the ortho-methyl groups of the sulfonyl benzene rings in all the mol­ecules. The sulfonyl and the aniline benzene rings are tilted relative to each other...

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Detalles Bibliográficos
Autores principales: Rodrigues, Vinola Z., Foro, Sabine, Gowda, B. Thimme
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247308/
https://www.ncbi.nlm.nih.gov/pubmed/22219926
http://dx.doi.org/10.1107/S1600536811040876
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author Rodrigues, Vinola Z.
Foro, Sabine
Gowda, B. Thimme
author_facet Rodrigues, Vinola Z.
Foro, Sabine
Gowda, B. Thimme
author_sort Rodrigues, Vinola Z.
collection PubMed
description The asymmetric unit of the title compound, C(15)H(16)ClNO(2)S, contains three independent moleules. The conformation of the N—H bonds are anti to the ortho-methyl groups of the sulfonyl benzene rings in all the mol­ecules. The sulfonyl and the aniline benzene rings are tilted relative to each other by 43.0 (2), 37.0 (2) and by 46.0 (1)° in the three mol­ecules. In the crystal, inter­molecular N—H⋯O hydrogen bonds link each of the mol­ecules into centrosymmetric dimers.
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spelling pubmed-32473082012-01-04 4-Chloro-N-(2,5-dimethyl­phen­yl)-2-methyl­benzene­sulfonamide Rodrigues, Vinola Z. Foro, Sabine Gowda, B. Thimme Acta Crystallogr Sect E Struct Rep Online Organic Papers The asymmetric unit of the title compound, C(15)H(16)ClNO(2)S, contains three independent moleules. The conformation of the N—H bonds are anti to the ortho-methyl groups of the sulfonyl benzene rings in all the mol­ecules. The sulfonyl and the aniline benzene rings are tilted relative to each other by 43.0 (2), 37.0 (2) and by 46.0 (1)° in the three mol­ecules. In the crystal, inter­molecular N—H⋯O hydrogen bonds link each of the mol­ecules into centrosymmetric dimers. International Union of Crystallography 2011-10-08 /pmc/articles/PMC3247308/ /pubmed/22219926 http://dx.doi.org/10.1107/S1600536811040876 Text en © Rodrigues et al. 2011 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.
Foro, Sabine
Gowda, B. Thimme
4-Chloro-N-(2,5-dimethyl­phen­yl)-2-methyl­benzene­sulfonamide
title 4-Chloro-N-(2,5-dimethyl­phen­yl)-2-methyl­benzene­sulfonamide
title_full 4-Chloro-N-(2,5-dimethyl­phen­yl)-2-methyl­benzene­sulfonamide
title_fullStr 4-Chloro-N-(2,5-dimethyl­phen­yl)-2-methyl­benzene­sulfonamide
title_full_unstemmed 4-Chloro-N-(2,5-dimethyl­phen­yl)-2-methyl­benzene­sulfonamide
title_short 4-Chloro-N-(2,5-dimethyl­phen­yl)-2-methyl­benzene­sulfonamide
title_sort 4-chloro-n-(2,5-dimethyl­phen­yl)-2-methyl­benzene­sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247308/
https://www.ncbi.nlm.nih.gov/pubmed/22219926
http://dx.doi.org/10.1107/S1600536811040876
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