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Acta Cryst. (2005). E61, o2395-o2397  [ doi:10.1107/S1600536805020222 ]

Racemic trans-4-phenylperhydropyran-3-ol

J. Hartung, I. Svoboda, P. Schmidt and H. Fuess

Abstract: In the title compound, C11H14O2, the tetrahydropyran ring adopts a 1C4 conformation, with the phenyl and the hydroxy substituents located in equatorial positions. Hydrogen bonding occurs in the solid state between hydroxy groups to link two molecules of (R,R)-trans-4-phenylperhydropyran-3-ol and two molecules of the (S,S)-enantiomer to provide tetramers.

Online 6 July 2005


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