<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>67(Pt 10)</volume><submitter>Rivera A</submitter><pubmed_abstract>The imidazolidine ring in the title compound, C(17)H(18)Cl(2)N(2)O(2), adopts a twist conformation. The observed conformation is stabilized by two intra-molecular O-H⋯N hydrogen bonds, with both N atoms acting as hydrogen-bond acceptors. The phenyl substituents are aligned at 70.0 (1) and 76.6 (1)° with respect to the best plane through the five atoms of the imidazolidine ring. Weak inter-molecular C-H⋯O inter-actions stabilize the crystal packing.</pubmed_abstract><journal>Acta crystallographica. Section E, Structure reports online</journal><pagination>o2581</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC3201546</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>4,4'-Dichloro-2,2'-[imidazolidine-1,3-diylbis(methylene)]diphenol.</pubmed_title><pmcid>PMC3201546</pmcid><pubmed_authors>Rios-Motta J</pubmed_authors><pubmed_authors>Dusek M</pubmed_authors><pubmed_authors>Sadat-Bernal J</pubmed_authors><pubmed_authors>Rivera A</pubmed_authors><pubmed_authors>Pojarova M</pubmed_authors></additional><is_claimable>false</is_claimable><name>4,4'-Dichloro-2,2'-[imidazolidine-1,3-diylbis(methylene)]diphenol.</name><description>The imidazolidine ring in the title compound, C(17)H(18)Cl(2)N(2)O(2), adopts a twist conformation. The observed conformation is stabilized by two intra-molecular O-H⋯N hydrogen bonds, with both N atoms acting as hydrogen-bond acceptors. The phenyl substituents are aligned at 70.0 (1) and 76.6 (1)° with respect to the best plane through the five atoms of the imidazolidine ring. Weak inter-molecular C-H⋯O inter-actions stabilize the crystal packing.</description><dates><release>2011-01-01T00:00:00Z</release><publication>2011 Oct</publication><modification>2025-04-05T10:24:43.994Z</modification><creation>2019-03-27T00:01:08Z</creation></dates><accession>S-EPMC3201546</accession><cross_references><pubmed>22065817</pubmed><doi>10.1107/S1600536811035677</doi></cross_references></HashMap>