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N-Phenylsuccinamic acid
In the crystal structure of the title compound, C(10)H(11)NO(3), the conformations of N—H and C=O bonds in the amide segment are anti to each other. Further, the conformations of the amide O atom and the carbonyl O atom of the acid segment are anti to each other and to the adjacent –CH(2) groups. Th...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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International Union of Crystallography
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051503/ https://www.ncbi.nlm.nih.gov/pubmed/21522943 http://dx.doi.org/10.1107/S160053681005364X |
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author | Gowda, B. Thimme Foro, Sabine Saraswathi, B. S. Fuess, Hartmut |
author_facet | Gowda, B. Thimme Foro, Sabine Saraswathi, B. S. Fuess, Hartmut |
author_sort | Gowda, B. Thimme |
collection | PubMed |
description | In the crystal structure of the title compound, C(10)H(11)NO(3), the conformations of N—H and C=O bonds in the amide segment are anti to each other. Further, the conformations of the amide O atom and the carbonyl O atom of the acid segment are anti to each other and to the adjacent –CH(2) groups. The C=O and O—H bonds of the acid group are in syn positions with respect to each other. In the crystal, the molecules are packed into infinite chains along the a axis through intermolecular N—H⋯O and O—H⋯O hydrogen bonds. |
format | Text |
id | pubmed-3051503 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-30515032011-04-26 N-Phenylsuccinamic acid Gowda, B. Thimme Foro, Sabine Saraswathi, B. S. Fuess, Hartmut Acta Crystallogr Sect E Struct Rep Online Organic Papers In the crystal structure of the title compound, C(10)H(11)NO(3), the conformations of N—H and C=O bonds in the amide segment are anti to each other. Further, the conformations of the amide O atom and the carbonyl O atom of the acid segment are anti to each other and to the adjacent –CH(2) groups. The C=O and O—H bonds of the acid group are in syn positions with respect to each other. In the crystal, the molecules are packed into infinite chains along the a axis through intermolecular N—H⋯O and O—H⋯O hydrogen bonds. International Union of Crystallography 2011-01-08 /pmc/articles/PMC3051503/ /pubmed/21522943 http://dx.doi.org/10.1107/S160053681005364X Text en © Gowda 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 Gowda, B. Thimme Foro, Sabine Saraswathi, B. S. Fuess, Hartmut N-Phenylsuccinamic acid |
title |
N-Phenylsuccinamic acid |
title_full |
N-Phenylsuccinamic acid |
title_fullStr |
N-Phenylsuccinamic acid |
title_full_unstemmed |
N-Phenylsuccinamic acid |
title_short |
N-Phenylsuccinamic acid |
title_sort | n-phenylsuccinamic acid |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3051503/ https://www.ncbi.nlm.nih.gov/pubmed/21522943 http://dx.doi.org/10.1107/S160053681005364X |
work_keys_str_mv | AT gowdabthimme nphenylsuccinamicacid AT forosabine nphenylsuccinamicacid AT saraswathibs nphenylsuccinamicacid AT fuesshartmut nphenylsuccinamicacid |