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4-Chloro-N-(2-chloro­benzo­yl)benzene­sulfonamide

In the structure of the title compound, C(13)H(9)Cl(2)NO(3)S, the conformation of the N—H bond in the C—SO(2)—NH—C(O) segment is anti to the C=O bond. The mol­ecule is twisted at the S atom with a torsion angle of 65.7 (2)°. The dihedral angle between the sulfonyl benzene ring and the —SO(2)—NH—C—O...

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Detalles Bibliográficos
Autores principales: Gowda, B. Thimme, Foro, Sabine, Suchetan, P. A., Fuess, Hartmut
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979439/
https://www.ncbi.nlm.nih.gov/pubmed/21579535
http://dx.doi.org/10.1107/S1600536810019057
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author Gowda, B. Thimme
Foro, Sabine
Suchetan, P. A.
Fuess, Hartmut
author_facet Gowda, B. Thimme
Foro, Sabine
Suchetan, P. A.
Fuess, Hartmut
author_sort Gowda, B. Thimme
collection PubMed
description In the structure of the title compound, C(13)H(9)Cl(2)NO(3)S, the conformation of the N—H bond in the C—SO(2)—NH—C(O) segment is anti to the C=O bond. The mol­ecule is twisted at the S atom with a torsion angle of 65.7 (2)°. The dihedral angle between the sulfonyl benzene ring and the —SO(2)—NH—C—O segment is 88.5 (1)°, and that between the sulfonyl and the benzoyl benzene rings is 58.0 (1)°. In the crystal, mol­ecules are linked by pairs of N—H⋯O hydrogen bonds, forming inversion dimers.
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spelling pubmed-29794392010-12-30 4-Chloro-N-(2-chloro­benzo­yl)benzene­sulfonamide Gowda, B. Thimme Foro, Sabine Suchetan, P. A. 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 conformation of the N—H bond in the C—SO(2)—NH—C(O) segment is anti to the C=O bond. The mol­ecule is twisted at the S atom with a torsion angle of 65.7 (2)°. The dihedral angle between the sulfonyl benzene ring and the —SO(2)—NH—C—O segment is 88.5 (1)°, and that between the sulfonyl and the benzoyl benzene rings is 58.0 (1)°. In the crystal, mol­ecules are linked by pairs of N—H⋯O hydrogen bonds, forming inversion dimers. International Union of Crystallography 2010-05-26 /pmc/articles/PMC2979439/ /pubmed/21579535 http://dx.doi.org/10.1107/S1600536810019057 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
Suchetan, P. A.
Fuess, Hartmut
4-Chloro-N-(2-chloro­benzo­yl)benzene­sulfonamide
title 4-Chloro-N-(2-chloro­benzo­yl)benzene­sulfonamide
title_full 4-Chloro-N-(2-chloro­benzo­yl)benzene­sulfonamide
title_fullStr 4-Chloro-N-(2-chloro­benzo­yl)benzene­sulfonamide
title_full_unstemmed 4-Chloro-N-(2-chloro­benzo­yl)benzene­sulfonamide
title_short 4-Chloro-N-(2-chloro­benzo­yl)benzene­sulfonamide
title_sort 4-chloro-n-(2-chloro­benzo­yl)benzene­sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979439/
https://www.ncbi.nlm.nih.gov/pubmed/21579535
http://dx.doi.org/10.1107/S1600536810019057
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AT fuesshartmut 4chloron2chlorobenzoylbenzenesulfonamide