2-Chloro-N-[(2-methyl­phen­yl)sulfon­yl]acetamide

In the title compound, C(9)H(10)ClNO(3)S, the amide H atom is syn with respect to the ortho-methyl group in the benzene ring and the C—S—N—C torsion angle is −66.9 (2)°. An intra­molecular N—H⋯Cl hydrogen bond occurs. The crystal structure features inversion-related dimers linked by pairs of N—H⋯O h...

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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:
Organic Papers
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051983/
https://www.ncbi.nlm.nih.gov/pubmed/21522316
http://dx.doi.org/10.1107/S1600536811003655
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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(9)H(10)ClNO(3)S, the amide H atom is syn with respect to the ortho-methyl group in the benzene ring and the C—S—N—C torsion angle is −66.9 (2)°. An intra­molecular N—H⋯Cl hydrogen bond occurs. The crystal structure features inversion-related dimers linked by pairs of N—H⋯O hydrogen bonds.
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spelling pubmed-30519832011-04-26 2-Chloro-N-[(2-methyl­phen­yl)sulfon­yl]acetamide Shakuntala, K. Foro, Sabine Gowda, B. Thimme Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(9)H(10)ClNO(3)S, the amide H atom is syn with respect to the ortho-methyl group in the benzene ring and the C—S—N—C torsion angle is −66.9 (2)°. An intra­molecular N—H⋯Cl hydrogen bond occurs. The crystal structure features inversion-related dimers linked by pairs of N—H⋯O hydrogen bonds. International Union of Crystallography 2011-02-02 /pmc/articles/PMC3051983/ /pubmed/21522316 http://dx.doi.org/10.1107/S1600536811003655 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
2-Chloro-N-[(2-methyl­phen­yl)sulfon­yl]acetamide
title 2-Chloro-N-[(2-methyl­phen­yl)sulfon­yl]acetamide
title_full 2-Chloro-N-[(2-methyl­phen­yl)sulfon­yl]acetamide
title_fullStr 2-Chloro-N-[(2-methyl­phen­yl)sulfon­yl]acetamide
title_full_unstemmed 2-Chloro-N-[(2-methyl­phen­yl)sulfon­yl]acetamide
title_short 2-Chloro-N-[(2-methyl­phen­yl)sulfon­yl]acetamide
title_sort 2-chloro-n-[(2-methyl­phen­yl)sulfon­yl]acetamide
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051983/
https://www.ncbi.nlm.nih.gov/pubmed/21522316
http://dx.doi.org/10.1107/S1600536811003655
work_keys_str_mv AT shakuntalak 2chloron2methylphenylsulfonylacetamide
AT forosabine 2chloron2methylphenylsulfonylacetamide
AT gowdabthimme 2chloron2methylphenylsulfonylacetamide

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