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7-Bromo-4-(7-bromo-3,3-dimethyl-1-oxo-2,3,4,9-tetra­hydro-1H-xanthen-9-yl)-3,3-dimethyl-2,3-dihydroxanthen-1(4H)-one ethanol solvate

The title compound, C(30)H(26)Br(2)O(4)·C(2)H(5)OH, was synthesized from the reaction between 5-bromo­salicybenzaldehyde and 5,5-dimethyl-1,3-cyclo­hexa­nedione. The crystal packing is stabilized by inter­molecular O—H⋯O hydrogen bonds and C—H⋯O inter­actions.

Detalles Bibliográficos
Autores principales: Lian, Chaomei, Lu, Pingping, Zhu, Yulin
Formato: Texto
Lenguaje:English
Publicado: International Union of Crystallography 2009
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970291/
https://www.ncbi.nlm.nih.gov/pubmed/21577903
http://dx.doi.org/10.1107/S1600536809035922
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author Lian, Chaomei
Lu, Pingping
Zhu, Yulin
author_facet Lian, Chaomei
Lu, Pingping
Zhu, Yulin
author_sort Lian, Chaomei
collection PubMed
description The title compound, C(30)H(26)Br(2)O(4)·C(2)H(5)OH, was synthesized from the reaction between 5-bromo­salicybenzaldehyde and 5,5-dimethyl-1,3-cyclo­hexa­nedione. The crystal packing is stabilized by inter­molecular O—H⋯O hydrogen bonds and C—H⋯O inter­actions.
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spelling pubmed-29702912010-12-30 7-Bromo-4-(7-bromo-3,3-dimethyl-1-oxo-2,3,4,9-tetra­hydro-1H-xanthen-9-yl)-3,3-dimethyl-2,3-dihydroxanthen-1(4H)-one ethanol solvate Lian, Chaomei Lu, Pingping Zhu, Yulin Acta Crystallogr Sect E Struct Rep Online Organic Papers The title compound, C(30)H(26)Br(2)O(4)·C(2)H(5)OH, was synthesized from the reaction between 5-bromo­salicybenzaldehyde and 5,5-dimethyl-1,3-cyclo­hexa­nedione. The crystal packing is stabilized by inter­molecular O—H⋯O hydrogen bonds and C—H⋯O inter­actions. International Union of Crystallography 2009-09-12 /pmc/articles/PMC2970291/ /pubmed/21577903 http://dx.doi.org/10.1107/S1600536809035922 Text en © Lian 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
Lian, Chaomei
Lu, Pingping
Zhu, Yulin
7-Bromo-4-(7-bromo-3,3-dimethyl-1-oxo-2,3,4,9-tetra­hydro-1H-xanthen-9-yl)-3,3-dimethyl-2,3-dihydroxanthen-1(4H)-one ethanol solvate
title 7-Bromo-4-(7-bromo-3,3-dimethyl-1-oxo-2,3,4,9-tetra­hydro-1H-xanthen-9-yl)-3,3-dimethyl-2,3-dihydroxanthen-1(4H)-one ethanol solvate
title_full 7-Bromo-4-(7-bromo-3,3-dimethyl-1-oxo-2,3,4,9-tetra­hydro-1H-xanthen-9-yl)-3,3-dimethyl-2,3-dihydroxanthen-1(4H)-one ethanol solvate
title_fullStr 7-Bromo-4-(7-bromo-3,3-dimethyl-1-oxo-2,3,4,9-tetra­hydro-1H-xanthen-9-yl)-3,3-dimethyl-2,3-dihydroxanthen-1(4H)-one ethanol solvate
title_full_unstemmed 7-Bromo-4-(7-bromo-3,3-dimethyl-1-oxo-2,3,4,9-tetra­hydro-1H-xanthen-9-yl)-3,3-dimethyl-2,3-dihydroxanthen-1(4H)-one ethanol solvate
title_short 7-Bromo-4-(7-bromo-3,3-dimethyl-1-oxo-2,3,4,9-tetra­hydro-1H-xanthen-9-yl)-3,3-dimethyl-2,3-dihydroxanthen-1(4H)-one ethanol solvate
title_sort 7-bromo-4-(7-bromo-3,3-dimethyl-1-oxo-2,3,4,9-tetra­hydro-1h-xanthen-9-yl)-3,3-dimethyl-2,3-dihydroxanthen-1(4h)-one ethanol solvate
topic Organic Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2970291/
https://www.ncbi.nlm.nih.gov/pubmed/21577903
http://dx.doi.org/10.1107/S1600536809035922
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AT lupingping 7bromo47bromo33dimethyl1oxo2349tetrahydro1hxanthen9yl33dimethyl23dihydroxanthen14honeethanolsolvate
AT zhuyulin 7bromo47bromo33dimethyl1oxo2349tetrahydro1hxanthen9yl33dimethyl23dihydroxanthen14honeethanolsolvate