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4-(Cyclopropanecarboxamido)benzoic acid
In the title compound, C(11)H(11)NO(3), the dihedral angle between the benzene ring and the cyclopropane ring is 63.2 (1)°. In the crystal, molecules are linked through classical cyclic carboxylic acid O—H⋯O hydrogen-bond interactions [graph set R (2) (2)(8)] giving centrosymmetric dimers which...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3470383/ https://www.ncbi.nlm.nih.gov/pubmed/23125796 http://dx.doi.org/10.1107/S1600536812038196 |
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author | Sun, Zhong-Qiang Ding, Zhen-Ya Shao, Zhi-Yu |
author_facet | Sun, Zhong-Qiang Ding, Zhen-Ya Shao, Zhi-Yu |
author_sort | Sun, Zhong-Qiang |
collection | PubMed |
description | In the title compound, C(11)H(11)NO(3), the dihedral angle between the benzene ring and the cyclopropane ring is 63.2 (1)°. In the crystal, molecules are linked through classical cyclic carboxylic acid O—H⋯O hydrogen-bond interactions [graph set R (2) (2)(8)] giving centrosymmetric dimers which are extended along the b-axis direction through amide N—H⋯O hydrogen-bond interactions, giving one-dimensional ribbon structures. Weak C—H⋯O interactions are also present in the structure. |
format | Online Article Text |
id | pubmed-3470383 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-34703832012-11-02 4-(Cyclopropanecarboxamido)benzoic acid Sun, Zhong-Qiang Ding, Zhen-Ya Shao, Zhi-Yu Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(11)H(11)NO(3), the dihedral angle between the benzene ring and the cyclopropane ring is 63.2 (1)°. In the crystal, molecules are linked through classical cyclic carboxylic acid O—H⋯O hydrogen-bond interactions [graph set R (2) (2)(8)] giving centrosymmetric dimers which are extended along the b-axis direction through amide N—H⋯O hydrogen-bond interactions, giving one-dimensional ribbon structures. Weak C—H⋯O interactions are also present in the structure. International Union of Crystallography 2012-09-29 /pmc/articles/PMC3470383/ /pubmed/23125796 http://dx.doi.org/10.1107/S1600536812038196 Text en © Sun et al. 2012 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 Sun, Zhong-Qiang Ding, Zhen-Ya Shao, Zhi-Yu 4-(Cyclopropanecarboxamido)benzoic acid |
title | 4-(Cyclopropanecarboxamido)benzoic acid |
title_full | 4-(Cyclopropanecarboxamido)benzoic acid |
title_fullStr | 4-(Cyclopropanecarboxamido)benzoic acid |
title_full_unstemmed | 4-(Cyclopropanecarboxamido)benzoic acid |
title_short | 4-(Cyclopropanecarboxamido)benzoic acid |
title_sort | 4-(cyclopropanecarboxamido)benzoic acid |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3470383/ https://www.ncbi.nlm.nih.gov/pubmed/23125796 http://dx.doi.org/10.1107/S1600536812038196 |
work_keys_str_mv | AT sunzhongqiang 4cyclopropanecarboxamidobenzoicacid AT dingzhenya 4cyclopropanecarboxamidobenzoicacid AT shaozhiyu 4cyclopropanecarboxamidobenzoicacid |