{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["65(Pt 8)"],"submitter":["Yin XJ"],"pubmed_abstract":["The title compound, C(21)H(21)BrO(7)·C(2)H(6)O, was synthesized by the Claisen-Schimidt reaction of helicid (systematic name: 4-formyl-phenyl-β-d-allopyran-oside) with 4-bromo-aceto-phenone in ethanol. The pyran ring adopts a chair conformation. In the crystal structure, mol-ecules are linked into a three-dimensional network by inter-molecular O-H⋯O hydrogen bonds."],"journal":["Acta crystallographica. Section E, Structure reports online"],"pagination":["o2044"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC2977370"],"repository":["biostudies-literature"],"pubmed_title":["(E)-4-(β-d-Allopyran-os-yloxy)cinnamyl 4-bromo-phenyl ketone ethanol solvate."],"pmcid":["PMC2977370"],"pubmed_authors":["Li Y","Zheng L","Yin SF","Yin XJ","Bai X"],"additional_accession":[]},"is_claimable":false,"name":"(E)-4-(β-d-Allopyran-os-yloxy)cinnamyl 4-bromo-phenyl ketone ethanol solvate.","description":"The title compound, C(21)H(21)BrO(7)·C(2)H(6)O, was synthesized by the Claisen-Schimidt reaction of helicid (systematic name: 4-formyl-phenyl-β-d-allopyran-oside) with 4-bromo-aceto-phenone in ethanol. The pyran ring adopts a chair conformation. In the crystal structure, mol-ecules are linked into a three-dimensional network by inter-molecular O-H⋯O hydrogen bonds.","dates":{"release":"2009-01-01T00:00:00Z","publication":"2009 Jul","modification":"2025-04-22T12:25:11.06Z","creation":"2019-03-27T00:00:55Z"},"accession":"S-EPMC2977370","cross_references":{"pubmed":["21583708"],"doi":["10.1107/S1600536809029687"]}}