biostudies-literatureUnknown67(Pt 8)Betz RThe 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.Acta crystallographica. Section E, Structure reports onlineo2180https://www.ebi.ac.uk/biostudies/studies/S-EPMC3213614biostudies-literature(2-Hy-droxy-4-meth-oxy-phen-yl)(2-hy-droxy-phen-yl)methanone.PMC3213614Hosten ESchalekamp HGerber TBetz Rfalse(2-Hy-droxy-4-meth-oxy-phen-yl)(2-hy-droxy-phen-yl)methanone.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.2011-01-01T00:00:00Z2011 Aug2025-04-05T09:13:12.82Z2019-03-27T00:01:09ZS-EPMC32136142209119110.1107/S1600536811030042