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2,5-Dichloro-N-(3-methyl­phen­yl)benzenesulfonamide

In the title compound, C(13)H(11)Cl(2)NO(2)S, the dihedral angle between the aromatic rings is 76.62 (10)° and the C—S—N—C linkage between the rings adopts a gauche conformation [torsion angle = −51.4 (2)°]. A weak intra­molecular C—H⋯O inter­action closes an S(6) ring. In the crystal, inversion dim...

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Autores principales: Mughal, Shumaila Younas, Khan, Islam Ullah, Harrison, William T. A., Khan, Muneeb Hayat, Arshad, Muhammad Nadeem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414931/
https://www.ncbi.nlm.nih.gov/pubmed/22904918
http://dx.doi.org/10.1107/S1600536812032023
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author Mughal, Shumaila Younas
Khan, Islam Ullah
Harrison, William T. A.
Khan, Muneeb Hayat
Arshad, Muhammad Nadeem
author_facet Mughal, Shumaila Younas
Khan, Islam Ullah
Harrison, William T. A.
Khan, Muneeb Hayat
Arshad, Muhammad Nadeem
author_sort Mughal, Shumaila Younas
collection PubMed
description In the title compound, C(13)H(11)Cl(2)NO(2)S, the dihedral angle between the aromatic rings is 76.62 (10)° and the C—S—N—C linkage between the rings adopts a gauche conformation [torsion angle = −51.4 (2)°]. A weak intra­molecular C—H⋯O inter­action closes an S(6) ring. In the crystal, inversion dimers linked by pairs of N—H⋯O hydrogen bonds generate R (2) (2)(8) loops.
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spelling pubmed-34149312012-08-17 2,5-Dichloro-N-(3-methyl­phen­yl)benzenesulfonamide Mughal, Shumaila Younas Khan, Islam Ullah Harrison, William T. A. Khan, Muneeb Hayat Arshad, Muhammad Nadeem Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(13)H(11)Cl(2)NO(2)S, the dihedral angle between the aromatic rings is 76.62 (10)° and the C—S—N—C linkage between the rings adopts a gauche conformation [torsion angle = −51.4 (2)°]. A weak intra­molecular C—H⋯O inter­action closes an S(6) ring. In the crystal, inversion dimers linked by pairs of N—H⋯O hydrogen bonds generate R (2) (2)(8) loops. International Union of Crystallography 2012-07-18 /pmc/articles/PMC3414931/ /pubmed/22904918 http://dx.doi.org/10.1107/S1600536812032023 Text en © Mughal et al. 2012 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
Mughal, Shumaila Younas
Khan, Islam Ullah
Harrison, William T. A.
Khan, Muneeb Hayat
Arshad, Muhammad Nadeem
2,5-Dichloro-N-(3-methyl­phen­yl)benzenesulfonamide
title 2,5-Dichloro-N-(3-methyl­phen­yl)benzenesulfonamide
title_full 2,5-Dichloro-N-(3-methyl­phen­yl)benzenesulfonamide
title_fullStr 2,5-Dichloro-N-(3-methyl­phen­yl)benzenesulfonamide
title_full_unstemmed 2,5-Dichloro-N-(3-methyl­phen­yl)benzenesulfonamide
title_short 2,5-Dichloro-N-(3-methyl­phen­yl)benzenesulfonamide
title_sort 2,5-dichloro-n-(3-methyl­phen­yl)benzenesulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3414931/
https://www.ncbi.nlm.nih.gov/pubmed/22904918
http://dx.doi.org/10.1107/S1600536812032023
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