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2-Chloro-N-(2-chlorobenzoyl)benzenesulfonamide
In the structure of the title compound, C(13)H(9)Cl(2)NO(3)S, the N—H bond is anti to the C=O bond and the dihedral angle between the two aromatic rings is 76.9 (1)°. In the crystal structure, molecules are linked by N—H⋯O(S) hydrogen bonds to form inversion dimers.
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2010
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979121/ https://www.ncbi.nlm.nih.gov/pubmed/21579101 http://dx.doi.org/10.1107/S1600536810012808 |
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author | Suchetan, P. A. Gowda, B. Thimme Foro, Sabine Fuess, Hartmut |
author_facet | Suchetan, P. A. Gowda, B. Thimme Foro, Sabine Fuess, Hartmut |
author_sort | Suchetan, P. A. |
collection | PubMed |
description | In the structure of the title compound, C(13)H(9)Cl(2)NO(3)S, the N—H bond is anti to the C=O bond and the dihedral angle between the two aromatic rings is 76.9 (1)°. In the crystal structure, molecules are linked by N—H⋯O(S) hydrogen bonds to form inversion dimers. |
format | Text |
id | pubmed-2979121 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29791212010-12-30 2-Chloro-N-(2-chlorobenzoyl)benzenesulfonamide Suchetan, P. A. Gowda, B. Thimme Foro, Sabine Fuess, Hartmut Acta Crystallogr Sect E Struct Rep Online Organic Papers In the structure of the title compound, C(13)H(9)Cl(2)NO(3)S, the N—H bond is anti to the C=O bond and the dihedral angle between the two aromatic rings is 76.9 (1)°. In the crystal structure, molecules are linked by N—H⋯O(S) hydrogen bonds to form inversion dimers. International Union of Crystallography 2010-04-10 /pmc/articles/PMC2979121/ /pubmed/21579101 http://dx.doi.org/10.1107/S1600536810012808 Text en © Suchetan 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 Suchetan, P. A. Gowda, B. Thimme Foro, Sabine Fuess, Hartmut 2-Chloro-N-(2-chlorobenzoyl)benzenesulfonamide |
title | 2-Chloro-N-(2-chlorobenzoyl)benzenesulfonamide |
title_full | 2-Chloro-N-(2-chlorobenzoyl)benzenesulfonamide |
title_fullStr | 2-Chloro-N-(2-chlorobenzoyl)benzenesulfonamide |
title_full_unstemmed | 2-Chloro-N-(2-chlorobenzoyl)benzenesulfonamide |
title_short | 2-Chloro-N-(2-chlorobenzoyl)benzenesulfonamide |
title_sort | 2-chloro-n-(2-chlorobenzoyl)benzenesulfonamide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979121/ https://www.ncbi.nlm.nih.gov/pubmed/21579101 http://dx.doi.org/10.1107/S1600536810012808 |
work_keys_str_mv | AT suchetanpa 2chloron2chlorobenzoylbenzenesulfonamide AT gowdabthimme 2chloron2chlorobenzoylbenzenesulfonamide AT forosabine 2chloron2chlorobenzoylbenzenesulfonamide AT fuesshartmut 2chloron2chlorobenzoylbenzenesulfonamide |