{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["67(Pt 8)"],"submitter":["Betz R"],"pubmed_abstract":["The title compound, C(14)H(12)O(4), is an asymmetric substitution product of benzophenone. Both hy-droxy groups are orientated towards the O atom of the keto group. Intra-molecular as well as inter-molecular O-H⋯O hydrogen bonds can be observed in the crystal structure, with the latter connecting the mol-ecules into chains along the crystallographic b axis. C-H⋯O contacts [C⋯O = 3.3297 (18) Å] are also apparent. The closest centroid-centroid distance between two aromatic systems is 4.9186 (9) Å."],"journal":["Acta crystallographica. Section E, Structure reports online"],"pagination":["o2180"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC3213614"],"repository":["biostudies-literature"],"pubmed_title":["(2-Hy-droxy-4-meth-oxy-phen-yl)(2-hy-droxy-phen-yl)methanone."],"pmcid":["PMC3213614"],"pubmed_authors":["Hosten E","Schalekamp H","Gerber T","Betz R"],"additional_accession":[]},"is_claimable":false,"name":"(2-Hy-droxy-4-meth-oxy-phen-yl)(2-hy-droxy-phen-yl)methanone.","description":"The title compound, C(14)H(12)O(4), is an asymmetric substitution product of benzophenone. Both hy-droxy groups are orientated towards the O atom of the keto group. Intra-molecular as well as inter-molecular O-H⋯O hydrogen bonds can be observed in the crystal structure, with the latter connecting the mol-ecules into chains along the crystallographic b axis. C-H⋯O contacts [C⋯O = 3.3297 (18) Å] are also apparent. The closest centroid-centroid distance between two aromatic systems is 4.9186 (9) Å.","dates":{"release":"2011-01-01T00:00:00Z","publication":"2011 Aug","modification":"2025-04-05T09:13:12.82Z","creation":"2019-03-27T00:01:09Z"},"accession":"S-EPMC3213614","cross_references":{"pubmed":["22091191"],"doi":["10.1107/S1600536811030042"]}}