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2-Allyloxy-5-nitrobenzoic acid
The molecule of the title compound, C(10)H(9)NO(5), is approximately planar, with the mean planes of the nitro, carboxyl and allyloxy groups rotated by 8.1 (3), 7.9 (3) and 4.52 (18)°, respectively, from the plane of the benzene ring. Bond lengths in the aromatic ring are influenced by both electr...
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/PMC2969386/ https://www.ncbi.nlm.nih.gov/pubmed/21582969 http://dx.doi.org/10.1107/S1600536809024179 |
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author | Ferreira, Valquiria B. N. Fiedler, Haidi D. Nome, Faruk Bortoluzzi, Adailton J. |
author_facet | Ferreira, Valquiria B. N. Fiedler, Haidi D. Nome, Faruk Bortoluzzi, Adailton J. |
author_sort | Ferreira, Valquiria B. N. |
collection | PubMed |
description | The molecule of the title compound, C(10)H(9)NO(5), is approximately planar, with the mean planes of the nitro, carboxyl and allyloxy groups rotated by 8.1 (3), 7.9 (3) and 4.52 (18)°, respectively, from the plane of the benzene ring. Bond lengths in the aromatic ring are influenced by both electronic effects and strain induced by ortho-substitution. In the crystal structure, centrosymmetrically related molecules are paired into dimers through strong O—H⋯O hydrogen bonds. |
format | Text |
id | pubmed-2969386 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29693862010-12-30 2-Allyloxy-5-nitrobenzoic acid Ferreira, Valquiria B. N. Fiedler, Haidi D. Nome, Faruk Bortoluzzi, Adailton J. Acta Crystallogr Sect E Struct Rep Online Organic Papers The molecule of the title compound, C(10)H(9)NO(5), is approximately planar, with the mean planes of the nitro, carboxyl and allyloxy groups rotated by 8.1 (3), 7.9 (3) and 4.52 (18)°, respectively, from the plane of the benzene ring. Bond lengths in the aromatic ring are influenced by both electronic effects and strain induced by ortho-substitution. In the crystal structure, centrosymmetrically related molecules are paired into dimers through strong O—H⋯O hydrogen bonds. International Union of Crystallography 2009-06-27 /pmc/articles/PMC2969386/ /pubmed/21582969 http://dx.doi.org/10.1107/S1600536809024179 Text en © Ferreira 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 Ferreira, Valquiria B. N. Fiedler, Haidi D. Nome, Faruk Bortoluzzi, Adailton J. 2-Allyloxy-5-nitrobenzoic acid |
title | 2-Allyloxy-5-nitrobenzoic acid |
title_full | 2-Allyloxy-5-nitrobenzoic acid |
title_fullStr | 2-Allyloxy-5-nitrobenzoic acid |
title_full_unstemmed | 2-Allyloxy-5-nitrobenzoic acid |
title_short | 2-Allyloxy-5-nitrobenzoic acid |
title_sort | 2-allyloxy-5-nitrobenzoic acid |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969386/ https://www.ncbi.nlm.nih.gov/pubmed/21582969 http://dx.doi.org/10.1107/S1600536809024179 |
work_keys_str_mv | AT ferreiravalquiriabn 2allyloxy5nitrobenzoicacid AT fiedlerhaidid 2allyloxy5nitrobenzoicacid AT nomefaruk 2allyloxy5nitrobenzoicacid AT bortoluzziadailtonj 2allyloxy5nitrobenzoicacid |