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N-(4-Chloro­phenyl­sulfon­yl)-2-methyl­propanamide

In the crystal structure of the title compound, C(10)H(12)ClNO(3)S, the N—C bond in the C—SO(2)—NH—C segment has a gauche torsion with respect to the S=O bonds. The mol­ecule is twisted at the S atom with a C—S—N—C torsion angle of −62.3 (3)°. The benzene ring and the SO(2)—NH—CO—C segment form a di...

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Detalles Bibliográficos
Autores principales: Nirmala, P. G., Foro, Sabine, Gowda, B. Thimme
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3200645/
https://www.ncbi.nlm.nih.gov/pubmed/22064939
http://dx.doi.org/10.1107/S1600536811031394
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author Nirmala, P. G.
Foro, Sabine
Gowda, B. Thimme
author_facet Nirmala, P. G.
Foro, Sabine
Gowda, B. Thimme
author_sort Nirmala, P. G.
collection PubMed
description In the crystal structure of the title compound, C(10)H(12)ClNO(3)S, the N—C bond in the C—SO(2)—NH—C segment has a gauche torsion with respect to the S=O bonds. The mol­ecule is twisted at the S atom with a C—S—N—C torsion angle of −62.3 (3)°. The benzene ring and the SO(2)—NH—CO—C segment form a dihedral angle of 89.3 (1)°. In the crystal, mol­ecules are linked by pairs of N—H⋯O hydrogen bonds into inversion dimers.
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spelling pubmed-32006452011-11-06 N-(4-Chloro­phenyl­sulfon­yl)-2-methyl­propanamide Nirmala, P. G. Foro, Sabine Gowda, B. Thimme Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound, C(10)H(12)ClNO(3)S, the N—C bond in the C—SO(2)—NH—C segment has a gauche torsion with respect to the S=O bonds. The mol­ecule is twisted at the S atom with a C—S—N—C torsion angle of −62.3 (3)°. The benzene ring and the SO(2)—NH—CO—C segment form a dihedral angle of 89.3 (1)°. In the crystal, mol­ecules are linked by pairs of N—H⋯O hydrogen bonds into inversion dimers. International Union of Crystallography 2011-08-06 /pmc/articles/PMC3200645/ /pubmed/22064939 http://dx.doi.org/10.1107/S1600536811031394 Text en © Nirmala et al. 2011 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.
Foro, Sabine
Gowda, B. Thimme
N-(4-Chloro­phenyl­sulfon­yl)-2-methyl­propanamide
title N-(4-Chloro­phenyl­sulfon­yl)-2-methyl­propanamide
title_full N-(4-Chloro­phenyl­sulfon­yl)-2-methyl­propanamide
title_fullStr N-(4-Chloro­phenyl­sulfon­yl)-2-methyl­propanamide
title_full_unstemmed N-(4-Chloro­phenyl­sulfon­yl)-2-methyl­propanamide
title_short N-(4-Chloro­phenyl­sulfon­yl)-2-methyl­propanamide
title_sort n-(4-chloro­phenyl­sulfon­yl)-2-methyl­propanamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3200645/
https://www.ncbi.nlm.nih.gov/pubmed/22064939
http://dx.doi.org/10.1107/S1600536811031394
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