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N-(3-Chlorophenyl)benzenesulfonamide
In the crystal structure of the title compound, C(12)H(10)ClNO(2)S, the N—H bond is trans to one of the S=O bonds. The two aromatic rings form a dihedral angle of 65.4 (1)°, compared with a value of 49.1 (1)° in N-(2-chlorophenyl)-benzenesulfonamide. The molecules are connected by intermolecula...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960722/ https://www.ncbi.nlm.nih.gov/pubmed/21201800 http://dx.doi.org/10.1107/S1600536808026895 |
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author | Gowda, B. Thimme Foro, Sabine Babitha, K. S. Fuess, Hartmut |
author_facet | Gowda, B. Thimme Foro, Sabine Babitha, K. S. Fuess, Hartmut |
author_sort | Gowda, B. Thimme |
collection | PubMed |
description | In the crystal structure of the title compound, C(12)H(10)ClNO(2)S, the N—H bond is trans to one of the S=O bonds. The two aromatic rings form a dihedral angle of 65.4 (1)°, compared with a value of 49.1 (1)° in N-(2-chlorophenyl)-benzenesulfonamide. The molecules are connected by intermolecular N—H⋯O hydrogen bonds into chains running along the b axis. |
format | Text |
id | pubmed-2960722 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29607222010-12-30 N-(3-Chlorophenyl)benzenesulfonamide Gowda, B. Thimme Foro, Sabine Babitha, K. S. Fuess, Hartmut Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound, C(12)H(10)ClNO(2)S, the N—H bond is trans to one of the S=O bonds. The two aromatic rings form a dihedral angle of 65.4 (1)°, compared with a value of 49.1 (1)° in N-(2-chlorophenyl)-benzenesulfonamide. The molecules are connected by intermolecular N—H⋯O hydrogen bonds into chains running along the b axis. International Union of Crystallography 2008-08-23 /pmc/articles/PMC2960722/ /pubmed/21201800 http://dx.doi.org/10.1107/S1600536808026895 Text en © Gowda et al. 2008 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 Babitha, K. S. Fuess, Hartmut N-(3-Chlorophenyl)benzenesulfonamide |
title |
N-(3-Chlorophenyl)benzenesulfonamide |
title_full |
N-(3-Chlorophenyl)benzenesulfonamide |
title_fullStr |
N-(3-Chlorophenyl)benzenesulfonamide |
title_full_unstemmed |
N-(3-Chlorophenyl)benzenesulfonamide |
title_short |
N-(3-Chlorophenyl)benzenesulfonamide |
title_sort | n-(3-chlorophenyl)benzenesulfonamide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2960722/ https://www.ncbi.nlm.nih.gov/pubmed/21201800 http://dx.doi.org/10.1107/S1600536808026895 |
work_keys_str_mv | AT gowdabthimme n3chlorophenylbenzenesulfonamide AT forosabine n3chlorophenylbenzenesulfonamide AT babithaks n3chlorophenylbenzenesulfonamide AT fuesshartmut n3chlorophenylbenzenesulfonamide |