<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>67(Pt 9)</volume><submitter>Karama U</submitter><pubmed_abstract>In the title compound, C(20)H(18)O(2), the central six-membered ring adopts a boat conformation and the terminal benzene rings make a dihedral angle of 42.66 (4)° with each other. In the crystal structure, the O-H group forms both an intra- and an inter-molecular O-H⋯O hydrogen bond; the former generates an S(5) ring and the latter leads to inversion-generated R(2) (2)(10) loops. The dimers are further linked into ribbons propagating along the a axis by C-H⋯O inter-actions, and the packing is consolidated by weak C-H⋯π inter-actions.</pubmed_abstract><journal>Acta crystallographica. Section E, Structure reports online</journal><pagination>o2487</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3200828</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>11-Hy-droxy-9-(prop-2-en-1-yl)-9,10-dihydro-9,10-propano-anthracen-12-one.</pubmed_title><pmcid>PMC3200828</pmcid><pubmed_authors>Arumugam N</pubmed_authors><pubmed_authors>Almansour AI</pubmed_authors><pubmed_authors>Razak IA</pubmed_authors><pubmed_authors>Karama U</pubmed_authors><pubmed_authors>Arshad S</pubmed_authors></additional><is_claimable>false</is_claimable><name>11-Hy-droxy-9-(prop-2-en-1-yl)-9,10-dihydro-9,10-propano-anthracen-12-one.</name><description>In the title compound, C(20)H(18)O(2), the central six-membered ring adopts a boat conformation and the terminal benzene rings make a dihedral angle of 42.66 (4)° with each other. In the crystal structure, the O-H group forms both an intra- and an inter-molecular O-H⋯O hydrogen bond; the former generates an S(5) ring and the latter leads to inversion-generated R(2) (2)(10) loops. The dimers are further linked into ribbons propagating along the a axis by C-H⋯O inter-actions, and the packing is consolidated by weak C-H⋯π inter-actions.</description><dates><release>2011-01-01T00:00:00Z</release><publication>2011 Sep</publication><modification>2025-04-04T08:06:18.666Z</modification><creation>2019-03-26T23:59:26Z</creation></dates><accession>S-EPMC3200828</accession><cross_references><pubmed>22059039</pubmed><doi>10.1107/S1600536811033538</doi></cross_references></HashMap>