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3-Hydroxy-1,2-dimethoxyanthraquinone
The title compound, C(16)H(12)O(5), was isolated from Morinda officinalis How. The anthraquinone ring system is almost planar, the dihedral angle between the two benzene rings being 1.12 (4)°. In the crystal structure, O—H⋯O and C—H⋯O hydrogen bonds link the moleculesin the crystallographic a-axis...
| Autores principales: | , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
International Union of Crystallography
2009
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969515/ https://www.ncbi.nlm.nih.gov/pubmed/21582815 http://dx.doi.org/10.1107/S1600536809021266 |
| _version_ | 1782190174596235264 |
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| author | Xu, Yong-Jun Yang, Xiao-Xi Zhao, Hong-Bin |
| author_facet | Xu, Yong-Jun Yang, Xiao-Xi Zhao, Hong-Bin |
| author_sort | Xu, Yong-Jun |
| collection | PubMed |
| description | The title compound, C(16)H(12)O(5), was isolated from Morinda officinalis How. The anthraquinone ring system is almost planar, the dihedral angle between the two benzene rings being 1.12 (4)°. In the crystal structure, O—H⋯O and C—H⋯O hydrogen bonds link the moleculesin the crystallographic a-axis direction. Weak π–π stacking interactions [centroid–centroid distance between symmetry-related benzene rings of 3.699 (4) Å] are also present. |
| format | Text |
| id | pubmed-2969515 |
| institution | National Center for Biotechnology Information |
| language | English |
| publishDate | 2009 |
| publisher | International Union of Crystallography |
| record_format | MEDLINE/PubMed |
| spelling | pubmed-29695152010-12-30 3-Hydroxy-1,2-dimethoxyanthraquinone Xu, Yong-Jun Yang, Xiao-Xi Zhao, Hong-Bin Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(16)H(12)O(5), was isolated from Morinda officinalis How. The anthraquinone ring system is almost planar, the dihedral angle between the two benzene rings being 1.12 (4)°. In the crystal structure, O—H⋯O and C—H⋯O hydrogen bonds link the moleculesin the crystallographic a-axis direction. Weak π–π stacking interactions [centroid–centroid distance between symmetry-related benzene rings of 3.699 (4) Å] are also present. International Union of Crystallography 2009-06-06 /pmc/articles/PMC2969515/ /pubmed/21582815 http://dx.doi.org/10.1107/S1600536809021266 Text en © Xu 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 Xu, Yong-Jun Yang, Xiao-Xi Zhao, Hong-Bin 3-Hydroxy-1,2-dimethoxyanthraquinone |
| title | 3-Hydroxy-1,2-dimethoxyanthraquinone |
| title_full | 3-Hydroxy-1,2-dimethoxyanthraquinone |
| title_fullStr | 3-Hydroxy-1,2-dimethoxyanthraquinone |
| title_full_unstemmed | 3-Hydroxy-1,2-dimethoxyanthraquinone |
| title_short | 3-Hydroxy-1,2-dimethoxyanthraquinone |
| title_sort | 3-hydroxy-1,2-dimethoxyanthraquinone |
| topic | Organic Papers |
| url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2969515/ https://www.ncbi.nlm.nih.gov/pubmed/21582815 http://dx.doi.org/10.1107/S1600536809021266 |
| work_keys_str_mv | AT xuyongjun 3hydroxy12dimethoxyanthraquinone AT yangxiaoxi 3hydroxy12dimethoxyanthraquinone AT zhaohongbin 3hydroxy12dimethoxyanthraquinone |