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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.

Detalles Bibliográficos
Autores principales: Suchetan, P. A., Gowda, B. Thimme, Foro, Sabine, Fuess, Hartmut
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2010
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.
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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
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AT gowdabthimme 2chloron2chlorobenzoylbenzenesulfonamide
AT forosabine 2chloron2chlorobenzoylbenzenesulfonamide
AT fuesshartmut 2chloron2chlorobenzoylbenzenesulfonamide