Abstract

In the title compound, C13H12O3, the pyran ring adopts a half-chair conformation with a C atom deviating from the least-squares plane of the remaining ring atoms by 0.606 (2) Å. This plane and that of the benzene ring make a dihedral angle of 44.18 (6)°. In the crystal, mol­ecules are linked through O—H⋯O hydrogen bonds into infinite chains along the b axis, and these chains are cross-linked by C—H⋯O hydrogen bonded into sheets lying parallel to the bc plane. The layers are further connected via C—H⋯π inter­actions to form a three-dimensional supra­molecular structure.

Highlights

  • In the title compound, C13H12O3, the pyran ring adopts a halfchair conformation with a C atom deviating from the leastsquares plane of the remaining ring atoms by 0.606 (2) Å

  • H atoms treated by a mixture of independent and constrained refinement max = 0.18 e Å3

  • H O hydrogen bonds into infinite chains along the b axis, and these chains are cross-linked by C—H O hydrogen bonded into sheets lying parallel to the bc plane

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Summary

Bruker APEXII CCD diffractometer

H atoms treated by a mixture of independent and constrained refinement max = 0.18 e Å3. C13H12O3, the pyran ring adopts a halfchair conformation with a C atom deviating from the leastsquares plane of the remaining ring atoms by 0.606 (2) Å. This plane and that of the benzene ring make a dihedral angle of. H O hydrogen bonds into infinite chains along the b axis, and these chains are cross-linked by C—H O hydrogen bonded into sheets lying parallel to the bc plane. The layers are further connected via C—H interactions to form a three-dimensional supramolecular structure

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