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N-(2-Chlorophenylsulfonyl)-2,2-dimethylpropanamide
In the title compound, C(11)H(14)ClNO(3)S, the C—S—N—C torsion angle is −61.69 (17)°. In the crystal, inversion dimers linked by pairs of N—H⋯O hydrogen bonds occur, generating R (2) (2)(8) loops.
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120501/ https://www.ncbi.nlm.nih.gov/pubmed/21754785 http://dx.doi.org/10.1107/S1600536811017429 |
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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(11)H(14)ClNO(3)S, the C—S—N—C torsion angle is −61.69 (17)°. In the crystal, inversion dimers linked by pairs of N—H⋯O hydrogen bonds occur, generating R (2) (2)(8) loops. |
format | Online Article Text |
id | pubmed-3120501 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-31205012011-07-13 N-(2-Chlorophenylsulfonyl)-2,2-dimethylpropanamide Shakuntala, K. Foro, Sabine Gowda, B. Thimme Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(11)H(14)ClNO(3)S, the C—S—N—C torsion angle is −61.69 (17)°. In the crystal, inversion dimers linked by pairs of N—H⋯O hydrogen bonds occur, generating R (2) (2)(8) loops. International Union of Crystallography 2011-05-14 /pmc/articles/PMC3120501/ /pubmed/21754785 http://dx.doi.org/10.1107/S1600536811017429 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)-2,2-dimethylpropanamide |
title |
N-(2-Chlorophenylsulfonyl)-2,2-dimethylpropanamide |
title_full |
N-(2-Chlorophenylsulfonyl)-2,2-dimethylpropanamide |
title_fullStr |
N-(2-Chlorophenylsulfonyl)-2,2-dimethylpropanamide |
title_full_unstemmed |
N-(2-Chlorophenylsulfonyl)-2,2-dimethylpropanamide |
title_short |
N-(2-Chlorophenylsulfonyl)-2,2-dimethylpropanamide |
title_sort | n-(2-chlorophenylsulfonyl)-2,2-dimethylpropanamide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3120501/ https://www.ncbi.nlm.nih.gov/pubmed/21754785 http://dx.doi.org/10.1107/S1600536811017429 |
work_keys_str_mv | AT shakuntalak n2chlorophenylsulfonyl22dimethylpropanamide AT forosabine n2chlorophenylsulfonyl22dimethylpropanamide AT gowdabthimme n2chlorophenylsulfonyl22dimethylpropanamide |