4-Chloro-N-(3-methyl­phen­yl)benzene­sulfonamide

In the crystal of the title compound, C(13)H(12)ClNO(2)S, the N—H bond is anti to the meta-methyl group in the aniline ring. The C—SO(2)—NH—C torsion angle is −57.6 (2)°. The sulfonyl and aniline benzene rings are tilted relative to each other by 84.7 (1)°. The crystal structure features inversion-r...

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Detalles Bibliográficos
Autores principales: Shakuntala, K., 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/PMC3120465/
https://www.ncbi.nlm.nih.gov/pubmed/21754899
http://dx.doi.org/10.1107/S1600536811019416
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author Shakuntala, K.
Foro, Sabine
Gowda, B. Thimme
author_facet Shakuntala, K.
Foro, Sabine
Gowda, B. Thimme
author_sort Shakuntala, K.
collection PubMed
description In the crystal of the title compound, C(13)H(12)ClNO(2)S, the N—H bond is anti to the meta-methyl group in the aniline ring. The C—SO(2)—NH—C torsion angle is −57.6 (2)°. The sulfonyl and aniline benzene rings are tilted relative to each other by 84.7 (1)°. The crystal structure features inversion-related dimers linked by pairs of N—H⋯O hydrogen bonds.
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spelling pubmed-31204652011-07-13 4-Chloro-N-(3-methyl­phen­yl)benzene­sulfonamide Shakuntala, K. Foro, Sabine Gowda, B. Thimme Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal of the title compound, C(13)H(12)ClNO(2)S, the N—H bond is anti to the meta-methyl group in the aniline ring. The C—SO(2)—NH—C torsion angle is −57.6 (2)°. The sulfonyl and aniline benzene rings are tilted relative to each other by 84.7 (1)°. The crystal structure features inversion-related dimers linked by pairs of N—H⋯O hydrogen bonds. International Union of Crystallography 2011-05-28 /pmc/articles/PMC3120465/ /pubmed/21754899 http://dx.doi.org/10.1107/S1600536811019416 Text en © Shakuntala 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
Shakuntala, K.
Foro, Sabine
Gowda, B. Thimme
4-Chloro-N-(3-methyl­phen­yl)benzene­sulfonamide
title 4-Chloro-N-(3-methyl­phen­yl)benzene­sulfonamide
title_full 4-Chloro-N-(3-methyl­phen­yl)benzene­sulfonamide
title_fullStr 4-Chloro-N-(3-methyl­phen­yl)benzene­sulfonamide
title_full_unstemmed 4-Chloro-N-(3-methyl­phen­yl)benzene­sulfonamide
title_short 4-Chloro-N-(3-methyl­phen­yl)benzene­sulfonamide
title_sort 4-chloro-n-(3-methyl­phen­yl)benzene­sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120465/
https://www.ncbi.nlm.nih.gov/pubmed/21754899
http://dx.doi.org/10.1107/S1600536811019416
work_keys_str_mv AT shakuntalak 4chloron3methylphenylbenzenesulfonamide
AT forosabine 4chloron3methylphenylbenzenesulfonamide
AT gowdabthimme 4chloron3methylphenylbenzenesulfonamide

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