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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)°...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2010
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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. |
format | Text |
id | pubmed-3007926 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
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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