Cargando…

2,4-Dichloro-N-(2,4-dimethyl­phen­yl)benzene­sulfonamide

In the title compound, C(14)H(13)Cl(2)NO(2)S, the C—SO(2)—NH—C torsion angle is −71.4 (4)°. The sulfonyl and aniline benzene rings are tilted relative to one another by 44.6 (1)°. The crystal structure features inversion-related dimers linked by pairs of N—H⋯O hydrogen bonds.

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:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247564/
https://www.ncbi.nlm.nih.gov/pubmed/22219869
http://dx.doi.org/10.1107/S1600536811039274
_version_ 1782220136176943104
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 In the title compound, C(14)H(13)Cl(2)NO(2)S, the C—SO(2)—NH—C torsion angle is −71.4 (4)°. The sulfonyl and aniline benzene rings are tilted relative to one another by 44.6 (1)°. The crystal structure features inversion-related dimers linked by pairs of N—H⋯O hydrogen bonds.
format Online
Article
Text
id pubmed-3247564
institution National Center for Biotechnology Information
language English
publishDate 2011
publisher International Union of Crystallography
record_format MEDLINE/PubMed
spelling pubmed-32475642012-01-04 2,4-Dichloro-N-(2,4-dimethyl­phen­yl)benzene­sulfonamide Rodrigues, Vinola Z. Foro, Sabine Gowda, B. Thimme Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(14)H(13)Cl(2)NO(2)S, the C—SO(2)—NH—C torsion angle is −71.4 (4)°. The sulfonyl and aniline benzene rings are tilted relative to one another by 44.6 (1)°. The crystal structure features inversion-related dimers linked by pairs of N—H⋯O hydrogen bonds. International Union of Crystallography 2011-10-05 /pmc/articles/PMC3247564/ /pubmed/22219869 http://dx.doi.org/10.1107/S1600536811039274 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
2,4-Dichloro-N-(2,4-dimethyl­phen­yl)benzene­sulfonamide
title 2,4-Dichloro-N-(2,4-dimethyl­phen­yl)benzene­sulfonamide
title_full 2,4-Dichloro-N-(2,4-dimethyl­phen­yl)benzene­sulfonamide
title_fullStr 2,4-Dichloro-N-(2,4-dimethyl­phen­yl)benzene­sulfonamide
title_full_unstemmed 2,4-Dichloro-N-(2,4-dimethyl­phen­yl)benzene­sulfonamide
title_short 2,4-Dichloro-N-(2,4-dimethyl­phen­yl)benzene­sulfonamide
title_sort 2,4-dichloro-n-(2,4-dimethyl­phen­yl)benzene­sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3247564/
https://www.ncbi.nlm.nih.gov/pubmed/22219869
http://dx.doi.org/10.1107/S1600536811039274
work_keys_str_mv AT rodriguesvinolaz 24dichloron24dimethylphenylbenzenesulfonamide
AT forosabine 24dichloron24dimethylphenylbenzenesulfonamide
AT gowdabthimme 24dichloron24dimethylphenylbenzenesulfonamide