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N-(2-Chloro­phenyl­sulfon­yl)-2-methyl­propanamide

In the title compound, C(10)H(12)ClNO(3)S, the amide H atom is syn with respect to the ortho-chloro group in the benzene ring and the C—S—N—C torsion angle is 64.35 (16)°. The benzene ring and the SO(2)—NH—CO—C segment form a dihedral angle of 87.4 (1)°. The crystal structure features inversion-rela...

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Detalles Bibliográficos
Autores principales: Shakuntala, K., Foro, Sabine, Gowda, B. Thimme
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052113/
https://www.ncbi.nlm.nih.gov/pubmed/21522354
http://dx.doi.org/10.1107/S1600536811004284
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author Shakuntala, K.
Foro, Sabine
Gowda, B. Thimme
author_facet Shakuntala, K.
Foro, Sabine
Gowda, B. Thimme
author_sort Shakuntala, K.
collection PubMed
description In the title compound, C(10)H(12)ClNO(3)S, the amide H atom is syn with respect to the ortho-chloro group in the benzene ring and the C—S—N—C torsion angle is 64.35 (16)°. The benzene ring and the SO(2)—NH—CO—C segment form a dihedral angle of 87.4 (1)°. The crystal structure features inversion-related dimers linked by pairs of N—H⋯O hydrogen bonds.
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spelling pubmed-30521132011-04-26 N-(2-Chloro­phenyl­sulfon­yl)-2-methyl­propanamide Shakuntala, K. Foro, Sabine Gowda, B. Thimme Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(10)H(12)ClNO(3)S, the amide H atom is syn with respect to the ortho-chloro group in the benzene ring and the C—S—N—C torsion angle is 64.35 (16)°. The benzene ring and the SO(2)—NH—CO—C segment form a dihedral angle of 87.4 (1)°. The crystal structure features inversion-related dimers linked by pairs of N—H⋯O hydrogen bonds. International Union of Crystallography 2011-02-09 /pmc/articles/PMC3052113/ /pubmed/21522354 http://dx.doi.org/10.1107/S1600536811004284 Text en © Shakuntala 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
Shakuntala, K.
Foro, Sabine
Gowda, B. Thimme
N-(2-Chloro­phenyl­sulfon­yl)-2-methyl­propanamide
title N-(2-Chloro­phenyl­sulfon­yl)-2-methyl­propanamide
title_full N-(2-Chloro­phenyl­sulfon­yl)-2-methyl­propanamide
title_fullStr N-(2-Chloro­phenyl­sulfon­yl)-2-methyl­propanamide
title_full_unstemmed N-(2-Chloro­phenyl­sulfon­yl)-2-methyl­propanamide
title_short N-(2-Chloro­phenyl­sulfon­yl)-2-methyl­propanamide
title_sort n-(2-chloro­phenyl­sulfon­yl)-2-methyl­propanamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3052113/
https://www.ncbi.nlm.nih.gov/pubmed/21522354
http://dx.doi.org/10.1107/S1600536811004284
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