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2,2-Dichloro-N-(4-methylphenylsulfonyl)acetamide
The N—H and C=O bonds in the title compound, C(9)H(9)Cl(2)NO(3)S, are trans to each other, similar to what is observed in 2,2,2-trimethyl-N-(phenylsulfonyl)acetamide and 2,2,2-trimethyl-N-(4-methylphenylsulfonyl)acetamide. The bond parameters in the title compound are also similar to those in t...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962122/ https://www.ncbi.nlm.nih.gov/pubmed/21203204 http://dx.doi.org/10.1107/S160053680802134X |
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author | Gowda, B. Thimme Foro, Sabine Nirmala, P. G. Sowmya, B. P. Fuess, Hartmut |
author_facet | Gowda, B. Thimme Foro, Sabine Nirmala, P. G. Sowmya, B. P. Fuess, Hartmut |
author_sort | Gowda, B. Thimme |
collection | PubMed |
description | The N—H and C=O bonds in the title compound, C(9)H(9)Cl(2)NO(3)S, are trans to each other, similar to what is observed in 2,2,2-trimethyl-N-(phenylsulfonyl)acetamide and 2,2,2-trimethyl-N-(4-methylphenylsulfonyl)acetamide. The bond parameters in the title compound are also similar to those in the aforementioned two structures. N—H⋯O hydrogen bonds connect the molecules into chains running along the a axis. |
format | Text |
id | pubmed-2962122 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29621222010-12-30 2,2-Dichloro-N-(4-methylphenylsulfonyl)acetamide Gowda, B. Thimme Foro, Sabine Nirmala, P. G. Sowmya, B. P. Fuess, Hartmut Acta Crystallogr Sect E Struct Rep Online Organic Papers The N—H and C=O bonds in the title compound, C(9)H(9)Cl(2)NO(3)S, are trans to each other, similar to what is observed in 2,2,2-trimethyl-N-(phenylsulfonyl)acetamide and 2,2,2-trimethyl-N-(4-methylphenylsulfonyl)acetamide. The bond parameters in the title compound are also similar to those in the aforementioned two structures. N—H⋯O hydrogen bonds connect the molecules into chains running along the a axis. International Union of Crystallography 2008-07-16 /pmc/articles/PMC2962122/ /pubmed/21203204 http://dx.doi.org/10.1107/S160053680802134X Text en © Gowda et al. 2008 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. Sowmya, B. P. Fuess, Hartmut 2,2-Dichloro-N-(4-methylphenylsulfonyl)acetamide |
title | 2,2-Dichloro-N-(4-methylphenylsulfonyl)acetamide |
title_full | 2,2-Dichloro-N-(4-methylphenylsulfonyl)acetamide |
title_fullStr | 2,2-Dichloro-N-(4-methylphenylsulfonyl)acetamide |
title_full_unstemmed | 2,2-Dichloro-N-(4-methylphenylsulfonyl)acetamide |
title_short | 2,2-Dichloro-N-(4-methylphenylsulfonyl)acetamide |
title_sort | 2,2-dichloro-n-(4-methylphenylsulfonyl)acetamide |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2962122/ https://www.ncbi.nlm.nih.gov/pubmed/21203204 http://dx.doi.org/10.1107/S160053680802134X |
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