N-(3,5-Dichloro­phen­yl)-2,4-dimethyl­benzene­sulfonamide

In the crystal structure of the title compound, C(14)H(13)Cl(2)NO(2)S, the conformation of the N—C bond in the C—SO(2)—NH—C segment has gauche torsions with respect to the S=O bonds. The mol­ecule is bent at the N atom, with an C—SO(2)—NH—C torsion angle of −54.9 (3)°. The two benzene rings are tilt...

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Detalles Bibliográficos
Autores principales: Nirmala, P. G., Gowda, B. Thimme, Foro, Sabine, 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/PMC2979206/
https://www.ncbi.nlm.nih.gov/pubmed/21579143
http://dx.doi.org/10.1107/S1600536810013504
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author Nirmala, P. G.
Gowda, B. Thimme
Foro, Sabine
Fuess, Hartmut
author_facet Nirmala, P. G.
Gowda, B. Thimme
Foro, Sabine
Fuess, Hartmut
author_sort Nirmala, P. G.
collection PubMed
description In the crystal structure of the title compound, C(14)H(13)Cl(2)NO(2)S, the conformation of the N—C bond in the C—SO(2)—NH—C segment has gauche torsions with respect to the S=O bonds. The mol­ecule is bent at the N atom, with an C—SO(2)—NH—C torsion angle of −54.9 (3)°. The two benzene rings are tilted relative to each other by 82.3 (2)°. The mol­ecules are linked into centrosymmetric R (2) (2)(8) motifs by N—H⋯O hydrogen bonds and C—H⋯π inter­actions along [100].
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spelling pubmed-29792062010-12-30 N-(3,5-Dichloro­phen­yl)-2,4-dimethyl­benzene­sulfonamide Nirmala, P. G. Gowda, B. Thimme Foro, Sabine Fuess, Hartmut Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound, C(14)H(13)Cl(2)NO(2)S, the conformation of the N—C bond in the C—SO(2)—NH—C segment has gauche torsions with respect to the S=O bonds. The mol­ecule is bent at the N atom, with an C—SO(2)—NH—C torsion angle of −54.9 (3)°. The two benzene rings are tilted relative to each other by 82.3 (2)°. The mol­ecules are linked into centrosymmetric R (2) (2)(8) motifs by N—H⋯O hydrogen bonds and C—H⋯π inter­actions along [100]. International Union of Crystallography 2010-04-17 /pmc/articles/PMC2979206/ /pubmed/21579143 http://dx.doi.org/10.1107/S1600536810013504 Text en © Nirmala 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
Nirmala, P. G.
Gowda, B. Thimme
Foro, Sabine
Fuess, Hartmut
N-(3,5-Dichloro­phen­yl)-2,4-dimethyl­benzene­sulfonamide
title N-(3,5-Dichloro­phen­yl)-2,4-dimethyl­benzene­sulfonamide
title_full N-(3,5-Dichloro­phen­yl)-2,4-dimethyl­benzene­sulfonamide
title_fullStr N-(3,5-Dichloro­phen­yl)-2,4-dimethyl­benzene­sulfonamide
title_full_unstemmed N-(3,5-Dichloro­phen­yl)-2,4-dimethyl­benzene­sulfonamide
title_short N-(3,5-Dichloro­phen­yl)-2,4-dimethyl­benzene­sulfonamide
title_sort n-(3,5-dichloro­phen­yl)-2,4-dimethyl­benzene­sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2979206/
https://www.ncbi.nlm.nih.gov/pubmed/21579143
http://dx.doi.org/10.1107/S1600536810013504
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