N-(2-Chloro­phen­yl)-4-methyl­benzene­sulfonamide

The mol­ecule of the title compound, C(13)H(12)ClNO(2)S, is bent at the S atom with a C—SO(2)—NH—C torsion angle of −54.8 (2)°. The dihedral angle between the two aromatic rings is 71.6 (1)°. An intra­molecular N—H⋯Cl hydrogen bond is observed. The crystal structure features inversion-related dimers...

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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/PMC2980162/
https://www.ncbi.nlm.nih.gov/pubmed/21580072
http://dx.doi.org/10.1107/S1600536809053756
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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 The mol­ecule of the title compound, C(13)H(12)ClNO(2)S, is bent at the S atom with a C—SO(2)—NH—C torsion angle of −54.8 (2)°. The dihedral angle between the two aromatic rings is 71.6 (1)°. An intra­molecular N—H⋯Cl hydrogen bond is observed. The crystal structure features inversion-related dimers formed by pairs of N—H⋯O hydrogen bonds.
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spelling pubmed-29801622010-12-30 N-(2-Chloro­phen­yl)-4-methyl­benzene­sulfonamide Gowda, B. Thimme Foro, Sabine Nirmala, P. G. Fuess, Hartmut Acta Crystallogr Sect E Struct Rep Online Organic Papers The mol­ecule of the title compound, C(13)H(12)ClNO(2)S, is bent at the S atom with a C—SO(2)—NH—C torsion angle of −54.8 (2)°. The dihedral angle between the two aromatic rings is 71.6 (1)°. An intra­molecular N—H⋯Cl hydrogen bond is observed. The crystal structure features inversion-related dimers formed by pairs of N—H⋯O hydrogen bonds. International Union of Crystallography 2009-12-19 /pmc/articles/PMC2980162/ /pubmed/21580072 http://dx.doi.org/10.1107/S1600536809053756 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
Nirmala, P. G.
Fuess, Hartmut
N-(2-Chloro­phen­yl)-4-methyl­benzene­sulfonamide
title N-(2-Chloro­phen­yl)-4-methyl­benzene­sulfonamide
title_full N-(2-Chloro­phen­yl)-4-methyl­benzene­sulfonamide
title_fullStr N-(2-Chloro­phen­yl)-4-methyl­benzene­sulfonamide
title_full_unstemmed N-(2-Chloro­phen­yl)-4-methyl­benzene­sulfonamide
title_short N-(2-Chloro­phen­yl)-4-methyl­benzene­sulfonamide
title_sort n-(2-chloro­phen­yl)-4-methyl­benzene­sulfonamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2980162/
https://www.ncbi.nlm.nih.gov/pubmed/21580072
http://dx.doi.org/10.1107/S1600536809053756
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AT fuesshartmut n2chlorophenyl4methylbenzenesulfonamide

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