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

The asymmetric unit of the title compound, C(14)H(14)ClNO(2)S, contains two independent mol­ecules, which are twisted at the S atoms with C—SO(2)—NH—C torsion angles of −69.4 (7)° and 66.0 (8)°. The sulfonyl and the anilino benzene rings are tilted relative to each other by 49.0 (4) and 61.7 (3)° in...

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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/PMC3213544/
https://www.ncbi.nlm.nih.gov/pubmed/22091121
http://dx.doi.org/10.1107/S1600536811028819
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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 The asymmetric unit of the title compound, C(14)H(14)ClNO(2)S, contains two independent mol­ecules, which are twisted at the S atoms with C—SO(2)—NH—C torsion angles of −69.4 (7)° and 66.0 (8)°. The sulfonyl and the anilino benzene rings are tilted relative to each other by 49.0 (4) and 61.7 (3)° in the two mol­ecules. In the crystal, the mol­ecules are linked into chains by N—H⋯O hydrogen bonds.
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spelling pubmed-32135442011-11-16 4-Chloro-N-(3,5-dimethyl­phen­yl)benzene­sulfonamide Shakuntala, K. Foro, Sabine Gowda, B. Thimme 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, which are twisted at the S atoms with C—SO(2)—NH—C torsion angles of −69.4 (7)° and 66.0 (8)°. The sulfonyl and the anilino benzene rings are tilted relative to each other by 49.0 (4) and 61.7 (3)° in the two mol­ecules. In the crystal, the mol­ecules are linked into chains by N—H⋯O hydrogen bonds. International Union of Crystallography 2011-07-23 /pmc/articles/PMC3213544/ /pubmed/22091121 http://dx.doi.org/10.1107/S1600536811028819 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-(3,5-dimethyl­phen­yl)benzene­sulfonamide
title 4-Chloro-N-(3,5-dimethyl­phen­yl)benzene­sulfonamide
title_full 4-Chloro-N-(3,5-dimethyl­phen­yl)benzene­sulfonamide
title_fullStr 4-Chloro-N-(3,5-dimethyl­phen­yl)benzene­sulfonamide
title_full_unstemmed 4-Chloro-N-(3,5-dimethyl­phen­yl)benzene­sulfonamide
title_short 4-Chloro-N-(3,5-dimethyl­phen­yl)benzene­sulfonamide
title_sort 4-chloro-n-(3,5-dimethyl­phen­yl)benzene­sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213544/
https://www.ncbi.nlm.nih.gov/pubmed/22091121
http://dx.doi.org/10.1107/S1600536811028819
work_keys_str_mv AT shakuntalak 4chloron35dimethylphenylbenzenesulfonamide
AT forosabine 4chloron35dimethylphenylbenzenesulfonamide
AT gowdabthimme 4chloron35dimethylphenylbenzenesulfonamide

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