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2-Chloro-N-(3-chloro­benzo­yl)benzene­sulfonamide

The asymmetric unit of the title compound, C(13)H(9)Cl(2)NO(3)S, contains two independent mol­ecules. The conformation of the C=O bond is anti to the meta-Cl group in the chloro­benzoyl group of one of the mol­ecules and syn in the other. The dihedral angles between the sulfonyl and benzoyl benzene...

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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/PMC2979644/
https://www.ncbi.nlm.nih.gov/pubmed/21579432
http://dx.doi.org/10.1107/S1600536810016909
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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 The asymmetric unit of the title compound, C(13)H(9)Cl(2)NO(3)S, contains two independent mol­ecules. The conformation of the C=O bond is anti to the meta-Cl group in the chloro­benzoyl group of one of the mol­ecules and syn in the other. The dihedral angles between the sulfonyl and benzoyl benzene rings are 77.8 (1) and 83.5 (1)°. In the crystal structure, two pairs of independent mol­ecules are linked into a tetra­mer by N—H⋯O hydrogen bonds.
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spelling pubmed-29796442010-12-30 2-Chloro-N-(3-chloro­benzo­yl)benzene­sulfonamide Gowda, B. Thimme Foro, Sabine Suchetan, P. A. Fuess, Hartmut Acta Crystallogr Sect E Struct Rep Online Organic Papers The asymmetric unit of the title compound, C(13)H(9)Cl(2)NO(3)S, contains two independent mol­ecules. The conformation of the C=O bond is anti to the meta-Cl group in the chloro­benzoyl group of one of the mol­ecules and syn in the other. The dihedral angles between the sulfonyl and benzoyl benzene rings are 77.8 (1) and 83.5 (1)°. In the crystal structure, two pairs of independent mol­ecules are linked into a tetra­mer by N—H⋯O hydrogen bonds. International Union of Crystallography 2010-05-15 /pmc/articles/PMC2979644/ /pubmed/21579432 http://dx.doi.org/10.1107/S1600536810016909 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
2-Chloro-N-(3-chloro­benzo­yl)benzene­sulfonamide
title 2-Chloro-N-(3-chloro­benzo­yl)benzene­sulfonamide
title_full 2-Chloro-N-(3-chloro­benzo­yl)benzene­sulfonamide
title_fullStr 2-Chloro-N-(3-chloro­benzo­yl)benzene­sulfonamide
title_full_unstemmed 2-Chloro-N-(3-chloro­benzo­yl)benzene­sulfonamide
title_short 2-Chloro-N-(3-chloro­benzo­yl)benzene­sulfonamide
title_sort 2-chloro-n-(3-chloro­benzo­yl)benzene­sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979644/
https://www.ncbi.nlm.nih.gov/pubmed/21579432
http://dx.doi.org/10.1107/S1600536810016909
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AT forosabine 2chloron3chlorobenzoylbenzenesulfonamide
AT suchetanpa 2chloron3chlorobenzoylbenzenesulfonamide
AT fuesshartmut 2chloron3chlorobenzoylbenzenesulfonamide