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4-Chloro-2-methyl-N-(4-methyl­phen­yl)benzene­sulfonamide

The asymmetric unit of the title compound, C(14)H(14)ClNO(2)S, contains two independent mol­ecules. The torsion angles of the C—SO(2)—NH—C segments in the two mol­ecules are −76.5 (5) and −48.3 (4)°. The two aromatic rings are tilted relative to each other by 76.6 (2)° in one mol­ecule and 70.7 (2)°...

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Detalles Bibliográficos
Autores principales: Gowda, B. Thimme, Foro, Sabine, Nirmala, P. G., Fuess, Hartmut
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3007926/
https://www.ncbi.nlm.nih.gov/pubmed/21588675
http://dx.doi.org/10.1107/S1600536810032320
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author Gowda, B. Thimme
Foro, Sabine
Nirmala, P. G.
Fuess, Hartmut
author_facet Gowda, B. Thimme
Foro, Sabine
Nirmala, P. G.
Fuess, Hartmut
author_sort Gowda, B. Thimme
collection PubMed
description The asymmetric unit of the title compound, C(14)H(14)ClNO(2)S, contains two independent mol­ecules. The torsion angles of the C—SO(2)—NH—C segments in the two mol­ecules are −76.5 (5) and −48.3 (4)°. The two aromatic rings are tilted relative to each other by 76.6 (2)° in one mol­ecule and 70.7 (2)° in the other. In the crystal structure, inter­molecular N—H⋯O hydrogen bonds link the mol­ecules into centrosymmetric dimers.
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spelling pubmed-30079262010-12-30 4-Chloro-2-methyl-N-(4-methyl­phen­yl)benzene­sulfonamide Gowda, B. Thimme Foro, Sabine Nirmala, P. G. Fuess, Hartmut Acta Crystallogr Sect E Struct Rep Online Organic Papers The asymmetric unit of the title compound, C(14)H(14)ClNO(2)S, contains two independent mol­ecules. The torsion angles of the C—SO(2)—NH—C segments in the two mol­ecules are −76.5 (5) and −48.3 (4)°. The two aromatic rings are tilted relative to each other by 76.6 (2)° in one mol­ecule and 70.7 (2)° in the other. In the crystal structure, inter­molecular N—H⋯O hydrogen bonds link the mol­ecules into centrosymmetric dimers. International Union of Crystallography 2010-08-18 /pmc/articles/PMC3007926/ /pubmed/21588675 http://dx.doi.org/10.1107/S1600536810032320 Text en © Gowda et al. 2010 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
Foro, Sabine
Nirmala, P. G.
Fuess, Hartmut
4-Chloro-2-methyl-N-(4-methyl­phen­yl)benzene­sulfonamide
title 4-Chloro-2-methyl-N-(4-methyl­phen­yl)benzene­sulfonamide
title_full 4-Chloro-2-methyl-N-(4-methyl­phen­yl)benzene­sulfonamide
title_fullStr 4-Chloro-2-methyl-N-(4-methyl­phen­yl)benzene­sulfonamide
title_full_unstemmed 4-Chloro-2-methyl-N-(4-methyl­phen­yl)benzene­sulfonamide
title_short 4-Chloro-2-methyl-N-(4-methyl­phen­yl)benzene­sulfonamide
title_sort 4-chloro-2-methyl-n-(4-methyl­phen­yl)benzene­sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3007926/
https://www.ncbi.nlm.nih.gov/pubmed/21588675
http://dx.doi.org/10.1107/S1600536810032320
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