N-Benzoyl-2-chloro­benzene­sulfonamide

In the crystal structure of the title compound, C(13)H(10)ClNO(3)S, the conformation of the of the N—H bond in the C—SO(2)—NH—C(O) segment is anti to the C=O bond. The dihedral angle between the two benzene rings is 73.3 (1)°. In the crystal, inversion dimers linked by pairs of N—H⋯O hydrogen bonds...

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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:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2984022/
https://www.ncbi.nlm.nih.gov/pubmed/21580633
http://dx.doi.org/10.1107/S1600536810008731
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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 crystal structure of the title compound, C(13)H(10)ClNO(3)S, the conformation of the of the N—H bond in the C—SO(2)—NH—C(O) segment is anti to the C=O bond. The dihedral angle between the two benzene rings is 73.3 (1)°. In the crystal, inversion dimers linked by pairs of N—H⋯O hydrogen bonds occur.
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spelling pubmed-29840222010-12-30 N-Benzoyl-2-chloro­benzene­sulfonamide Gowda, B. Thimme Foro, Sabine Suchetan, P. A. Fuess, Hartmut Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound, C(13)H(10)ClNO(3)S, the conformation of the of the N—H bond in the C—SO(2)—NH—C(O) segment is anti to the C=O bond. The dihedral angle between the two benzene rings is 73.3 (1)°. In the crystal, inversion dimers linked by pairs of N—H⋯O hydrogen bonds occur. International Union of Crystallography 2010-03-13 /pmc/articles/PMC2984022/ /pubmed/21580633 http://dx.doi.org/10.1107/S1600536810008731 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
N-Benzoyl-2-chloro­benzene­sulfonamide
title N-Benzoyl-2-chloro­benzene­sulfonamide
title_full N-Benzoyl-2-chloro­benzene­sulfonamide
title_fullStr N-Benzoyl-2-chloro­benzene­sulfonamide
title_full_unstemmed N-Benzoyl-2-chloro­benzene­sulfonamide
title_short N-Benzoyl-2-chloro­benzene­sulfonamide
title_sort n-benzoyl-2-chloro­benzene­sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2984022/
https://www.ncbi.nlm.nih.gov/pubmed/21580633
http://dx.doi.org/10.1107/S1600536810008731
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AT forosabine nbenzoyl2chlorobenzenesulfonamide
AT suchetanpa nbenzoyl2chlorobenzenesulfonamide
AT fuesshartmut nbenzoyl2chlorobenzenesulfonamide

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