2,4-Dichloro-N-(3,4-dichloro­phen­yl)benzene­sulfonamide

In the crystal structure of the title compound, C(12)H(7)Cl(4)NO(2)S, the conformation of the N—H bond is syn to the meta-chloro residue in the aniline benzene ring. The two aromatic rings are tilted relative to each other by 68.9 (1)°. N—H⋯O hydrogen bonds connect the mol­ecules into centrosymmetri...

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Detalles Bibliográficos
Autores principales: Gowda, B. Thimme, Foro, Sabine, Nirmala, P. G., Fuess, Hartmut
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977279/
https://www.ncbi.nlm.nih.gov/pubmed/21583622
http://dx.doi.org/10.1107/S1600536809027883
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author Gowda, B. Thimme
Foro, Sabine
Nirmala, P. G.
Fuess, Hartmut
author_facet Gowda, B. Thimme
Foro, Sabine
Nirmala, P. G.
Fuess, Hartmut
author_sort Gowda, B. Thimme
collection PubMed
description In the crystal structure of the title compound, C(12)H(7)Cl(4)NO(2)S, the conformation of the N—H bond is syn to the meta-chloro residue in the aniline benzene ring. The two aromatic rings are tilted relative to each other by 68.9 (1)°. N—H⋯O hydrogen bonds connect the mol­ecules into centrosymmetric dimers.
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spelling pubmed-29772792010-12-30 2,4-Dichloro-N-(3,4-dichloro­phen­yl)benzene­sulfonamide Gowda, B. Thimme Foro, Sabine Nirmala, P. G. Fuess, Hartmut Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound, C(12)H(7)Cl(4)NO(2)S, the conformation of the N—H bond is syn to the meta-chloro residue in the aniline benzene ring. The two aromatic rings are tilted relative to each other by 68.9 (1)°. N—H⋯O hydrogen bonds connect the mol­ecules into centrosymmetric dimers. International Union of Crystallography 2009-07-22 /pmc/articles/PMC2977279/ /pubmed/21583622 http://dx.doi.org/10.1107/S1600536809027883 Text en © Gowda et al. 2009 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
Nirmala, P. G.
Fuess, Hartmut
2,4-Dichloro-N-(3,4-dichloro­phen­yl)benzene­sulfonamide
title 2,4-Dichloro-N-(3,4-dichloro­phen­yl)benzene­sulfonamide
title_full 2,4-Dichloro-N-(3,4-dichloro­phen­yl)benzene­sulfonamide
title_fullStr 2,4-Dichloro-N-(3,4-dichloro­phen­yl)benzene­sulfonamide
title_full_unstemmed 2,4-Dichloro-N-(3,4-dichloro­phen­yl)benzene­sulfonamide
title_short 2,4-Dichloro-N-(3,4-dichloro­phen­yl)benzene­sulfonamide
title_sort 2,4-dichloro-n-(3,4-dichloro­phen­yl)benzene­sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977279/
https://www.ncbi.nlm.nih.gov/pubmed/21583622
http://dx.doi.org/10.1107/S1600536809027883
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AT forosabine 24dichloron34dichlorophenylbenzenesulfonamide
AT nirmalapg 24dichloron34dichlorophenylbenzenesulfonamide
AT fuesshartmut 24dichloron34dichlorophenylbenzenesulfonamide

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