Cargando…
2,4-Dichloro-N-(3,4-dimethylphenyl)benzenesulfonamide
In the title compound, C(14)H(13)Cl(2)NO(2)S, the C—SO(2)—NH—C torsion angle is −60.84 (18). The sulfonyl and the aniline benzene rings are tilted relative to each other by 66.4 (1)°. The crystal structure features inversion-related dimers linked by pairs of N—H⋯O hydrogen bonds.
Autores principales: | , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3201316/ https://www.ncbi.nlm.nih.gov/pubmed/22065408 http://dx.doi.org/10.1107/S1600536811038256 |
_version_ | 1782214846429790208 |
---|---|
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 −60.84 (18). The sulfonyl and the aniline benzene rings are tilted relative to each other by 66.4 (1)°. The crystal structure features inversion-related dimers linked by pairs of N—H⋯O hydrogen bonds. |
format | Online Article Text |
id | pubmed-3201316 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-32013162011-11-06 2,4-Dichloro-N-(3,4-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 −60.84 (18). The sulfonyl and the aniline benzene rings are tilted relative to each other by 66.4 (1)°. The crystal structure features inversion-related dimers linked by pairs of N—H⋯O hydrogen bonds. International Union of Crystallography 2011-09-30 /pmc/articles/PMC3201316/ /pubmed/22065408 http://dx.doi.org/10.1107/S1600536811038256 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-(3,4-dimethylphenyl)benzenesulfonamide |
title | 2,4-Dichloro-N-(3,4-dimethylphenyl)benzenesulfonamide |
title_full | 2,4-Dichloro-N-(3,4-dimethylphenyl)benzenesulfonamide |
title_fullStr | 2,4-Dichloro-N-(3,4-dimethylphenyl)benzenesulfonamide |
title_full_unstemmed | 2,4-Dichloro-N-(3,4-dimethylphenyl)benzenesulfonamide |
title_short | 2,4-Dichloro-N-(3,4-dimethylphenyl)benzenesulfonamide |
title_sort | 2,4-dichloro-n-(3,4-dimethylphenyl)benzenesulfonamide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3201316/ https://www.ncbi.nlm.nih.gov/pubmed/22065408 http://dx.doi.org/10.1107/S1600536811038256 |
work_keys_str_mv | AT rodriguesvinolaz 24dichloron34dimethylphenylbenzenesulfonamide AT forosabine 24dichloron34dimethylphenylbenzenesulfonamide AT gowdabthimme 24dichloron34dimethylphenylbenzenesulfonamide |