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N-(3,5-Dichlorophenyl)-2-nitrobenzenesulfonamide
In the title compound, C(12)H(8)Cl(2)N(2)O(4)S, the C—S—N—C torsion angle is 49.34 (18)° and the dihedral angle between the benzene rings is 71.92 (10)°. The amide H atom exhibits bifurcated hydrogen bonding. The N—H bond is syn to the ortho-nitro group enabling the formation of an S(7) loop. In the...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3589054/ https://www.ncbi.nlm.nih.gov/pubmed/23476290 http://dx.doi.org/10.1107/S1600536812048283 |
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author | Chaithanya, U. Foro, Sabine Gowda, B. Thimme |
author_facet | Chaithanya, U. Foro, Sabine Gowda, B. Thimme |
author_sort | Chaithanya, U. |
collection | PubMed |
description | In the title compound, C(12)H(8)Cl(2)N(2)O(4)S, the C—S—N—C torsion angle is 49.34 (18)° and the dihedral angle between the benzene rings is 71.92 (10)°. The amide H atom exhibits bifurcated hydrogen bonding. The N—H bond is syn to the ortho-nitro group enabling the formation of an S(7) loop. In the crystal, pairs of N—H⋯O(S) hydrogen bonds link the molecules into inversion dimers via R (2) (2)(8) rings. |
format | Online Article Text |
id | pubmed-3589054 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-35890542013-03-08 N-(3,5-Dichlorophenyl)-2-nitrobenzenesulfonamide Chaithanya, U. Foro, Sabine Gowda, B. Thimme Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(12)H(8)Cl(2)N(2)O(4)S, the C—S—N—C torsion angle is 49.34 (18)° and the dihedral angle between the benzene rings is 71.92 (10)°. The amide H atom exhibits bifurcated hydrogen bonding. The N—H bond is syn to the ortho-nitro group enabling the formation of an S(7) loop. In the crystal, pairs of N—H⋯O(S) hydrogen bonds link the molecules into inversion dimers via R (2) (2)(8) rings. International Union of Crystallography 2012-11-30 /pmc/articles/PMC3589054/ /pubmed/23476290 http://dx.doi.org/10.1107/S1600536812048283 Text en © Chaithanya et al. 2012 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 Chaithanya, U. Foro, Sabine Gowda, B. Thimme N-(3,5-Dichlorophenyl)-2-nitrobenzenesulfonamide |
title |
N-(3,5-Dichlorophenyl)-2-nitrobenzenesulfonamide |
title_full |
N-(3,5-Dichlorophenyl)-2-nitrobenzenesulfonamide |
title_fullStr |
N-(3,5-Dichlorophenyl)-2-nitrobenzenesulfonamide |
title_full_unstemmed |
N-(3,5-Dichlorophenyl)-2-nitrobenzenesulfonamide |
title_short |
N-(3,5-Dichlorophenyl)-2-nitrobenzenesulfonamide |
title_sort | n-(3,5-dichlorophenyl)-2-nitrobenzenesulfonamide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3589054/ https://www.ncbi.nlm.nih.gov/pubmed/23476290 http://dx.doi.org/10.1107/S1600536812048283 |
work_keys_str_mv | AT chaithanyau n35dichlorophenyl2nitrobenzenesulfonamide AT forosabine n35dichlorophenyl2nitrobenzenesulfonamide AT gowdabthimme n35dichlorophenyl2nitrobenzenesulfonamide |