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N-(4-Chlorophenyl)succinamic acid
In the title compound, C(10)H(10)ClNO(3), the conformation of the amide O atom and the carbonyl O atom of the acid segment are anti to each other and further, they are anti to the H atoms of their adjacent –CH(2) groups. The C=O and O—H bonds of the acid group are in the syn position relative to eac...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977089/ https://www.ncbi.nlm.nih.gov/pubmed/21583529 http://dx.doi.org/10.1107/S160053680902649X |
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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 title compound, C(10)H(10)ClNO(3), the conformation of the amide O atom and the carbonyl O atom of the acid segment are anti to each other and further, they are anti to the H atoms of their adjacent –CH(2) groups. The C=O and O—H bonds of the acid group are in the syn position relative to each other. In the crystal, molecules are packed into infinite chains through intermolecular N—H⋯O and O—H⋯O hydrogen bonds. |
format | Text |
id | pubmed-2977089 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29770892010-12-30 N-(4-Chlorophenyl)succinamic acid Gowda, B. Thimme Foro, Sabine Saraswathi, B. S. Fuess, Hartmut Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(10)H(10)ClNO(3), the conformation of the amide O atom and the carbonyl O atom of the acid segment are anti to each other and further, they are anti to the H atoms of their adjacent –CH(2) groups. The C=O and O—H bonds of the acid group are in the syn position relative to each other. In the crystal, molecules are packed into infinite chains through intermolecular N—H⋯O and O—H⋯O hydrogen bonds. International Union of Crystallography 2009-07-11 /pmc/articles/PMC2977089/ /pubmed/21583529 http://dx.doi.org/10.1107/S160053680902649X Text en © Gowda et al. 2009 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-(4-Chlorophenyl)succinamic acid |
title |
N-(4-Chlorophenyl)succinamic acid |
title_full |
N-(4-Chlorophenyl)succinamic acid |
title_fullStr |
N-(4-Chlorophenyl)succinamic acid |
title_full_unstemmed |
N-(4-Chlorophenyl)succinamic acid |
title_short |
N-(4-Chlorophenyl)succinamic acid |
title_sort | n-(4-chlorophenyl)succinamic acid |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2977089/ https://www.ncbi.nlm.nih.gov/pubmed/21583529 http://dx.doi.org/10.1107/S160053680902649X |
work_keys_str_mv | AT gowdabthimme n4chlorophenylsuccinamicacid AT forosabine n4chlorophenylsuccinamicacid AT saraswathibs n4chlorophenylsuccinamicacid AT fuesshartmut n4chlorophenylsuccinamicacid |