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2,4-Dichloro-N-(3-chlorophenyl)benzenesulfonamide
In the title compound, C(12)H(8)Cl(3)NO(2)S, the conformation of the N—H bond in the C—SO(2)—NH—C segment is anti to the meta-Cl in the aniline ring. The molecule is twisted at the S atom, the C—SO(2)—NH—C torsion angle being 62.3 (2)°. The dihedral angle between the two benzene rings is 69.3 (1)°....
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/PMC3006719/ https://www.ncbi.nlm.nih.gov/pubmed/21587797 http://dx.doi.org/10.1107/S1600536810020349 |
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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 | In the title compound, C(12)H(8)Cl(3)NO(2)S, the conformation of the N—H bond in the C—SO(2)—NH—C segment is anti to the meta-Cl in the aniline ring. The molecule is twisted at the S atom, the C—SO(2)—NH—C torsion angle being 62.3 (2)°. The dihedral angle between the two benzene rings is 69.3 (1)°. The crystal structure features inversion dimers linked by pairs of N—H⋯O hydrogen bonds. |
format | Text |
id | pubmed-3006719 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-30067192010-12-30 2,4-Dichloro-N-(3-chlorophenyl)benzenesulfonamide Gowda, B. Thimme Foro, Sabine Nirmala, P. G. Fuess, Hartmut Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(12)H(8)Cl(3)NO(2)S, the conformation of the N—H bond in the C—SO(2)—NH—C segment is anti to the meta-Cl in the aniline ring. The molecule is twisted at the S atom, the C—SO(2)—NH—C torsion angle being 62.3 (2)°. The dihedral angle between the two benzene rings is 69.3 (1)°. The crystal structure features inversion dimers linked by pairs of N—H⋯O hydrogen bonds. International Union of Crystallography 2010-06-05 /pmc/articles/PMC3006719/ /pubmed/21587797 http://dx.doi.org/10.1107/S1600536810020349 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 2,4-Dichloro-N-(3-chlorophenyl)benzenesulfonamide |
title | 2,4-Dichloro-N-(3-chlorophenyl)benzenesulfonamide |
title_full | 2,4-Dichloro-N-(3-chlorophenyl)benzenesulfonamide |
title_fullStr | 2,4-Dichloro-N-(3-chlorophenyl)benzenesulfonamide |
title_full_unstemmed | 2,4-Dichloro-N-(3-chlorophenyl)benzenesulfonamide |
title_short | 2,4-Dichloro-N-(3-chlorophenyl)benzenesulfonamide |
title_sort | 2,4-dichloro-n-(3-chlorophenyl)benzenesulfonamide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3006719/ https://www.ncbi.nlm.nih.gov/pubmed/21587797 http://dx.doi.org/10.1107/S1600536810020349 |
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