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8-Hydroxy-5,6,7-trimethoxy-2-phenyl-4H-chromen-4-one
In the title compound, C(18)H(16)O(6), the benzopyran group is essentially planar, with the O atoms of the substituent groups lying close to its mean plane. The molecular conformation is governed by intramolecular interactions. The crystal packing is mainly determined by one classical intermolec...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
International Union of Crystallography
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961207/ https://www.ncbi.nlm.nih.gov/pubmed/21202382 http://dx.doi.org/10.1107/S1600536808010696 |
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author | Theodoro, Jahyr E. Santos, Djalma Pérez, Hiram da Silva, Maria Fátima das Graças Fernandes Ellena, J. |
author_facet | Theodoro, Jahyr E. Santos, Djalma Pérez, Hiram da Silva, Maria Fátima das Graças Fernandes Ellena, J. |
author_sort | Theodoro, Jahyr E. |
collection | PubMed |
description | In the title compound, C(18)H(16)O(6), the benzopyran group is essentially planar, with the O atoms of the substituent groups lying close to its mean plane. The molecular conformation is governed by intramolecular interactions. The crystal packing is mainly determined by one classical intermolecular hydrogen bond which gives rise to the formation of an infinite chain along the a axis. |
format | Text |
id | pubmed-2961207 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | International Union of Crystallography |
record_format | MEDLINE/PubMed |
spelling | pubmed-29612072010-12-30 8-Hydroxy-5,6,7-trimethoxy-2-phenyl-4H-chromen-4-one Theodoro, Jahyr E. Santos, Djalma Pérez, Hiram da Silva, Maria Fátima das Graças Fernandes Ellena, J. Acta Crystallogr Sect E Struct Rep Online Organic Papers In the title compound, C(18)H(16)O(6), the benzopyran group is essentially planar, with the O atoms of the substituent groups lying close to its mean plane. The molecular conformation is governed by intramolecular interactions. The crystal packing is mainly determined by one classical intermolecular hydrogen bond which gives rise to the formation of an infinite chain along the a axis. International Union of Crystallography 2008-04-23 /pmc/articles/PMC2961207/ /pubmed/21202382 http://dx.doi.org/10.1107/S1600536808010696 Text en © Theodoro et al. 2008 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 Theodoro, Jahyr E. Santos, Djalma Pérez, Hiram da Silva, Maria Fátima das Graças Fernandes Ellena, J. 8-Hydroxy-5,6,7-trimethoxy-2-phenyl-4H-chromen-4-one |
title | 8-Hydroxy-5,6,7-trimethoxy-2-phenyl-4H-chromen-4-one |
title_full | 8-Hydroxy-5,6,7-trimethoxy-2-phenyl-4H-chromen-4-one |
title_fullStr | 8-Hydroxy-5,6,7-trimethoxy-2-phenyl-4H-chromen-4-one |
title_full_unstemmed | 8-Hydroxy-5,6,7-trimethoxy-2-phenyl-4H-chromen-4-one |
title_short | 8-Hydroxy-5,6,7-trimethoxy-2-phenyl-4H-chromen-4-one |
title_sort | 8-hydroxy-5,6,7-trimethoxy-2-phenyl-4h-chromen-4-one |
topic | Organic Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2961207/ https://www.ncbi.nlm.nih.gov/pubmed/21202382 http://dx.doi.org/10.1107/S1600536808010696 |
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