Isolation and crystal structure of lawinal

The structure of the natural product lawinal [systematic name: (−)-(2S)-5,7-dihy­droxy-6-methyl-4-oxo-2-phenyl­chromane-8-carbaldehyde, C(17)H(14)O(5)] at 150 K is reported. The compound crystallizes with monoclinic (I2) symmetry and with Z′ = 2. The absolute configuration could not be determined reliably from X-ray analysis only. However, our analysis returns the S-configuration at the C-2 position, consistent with previous stereochemical assignment from specific rotation. The independent mol­ecules form into alternating hydrogen-bonded chains with C—H⋯O=CH inter­molecular linkages that run parallel to the crystallographic a axis and are extended into the ac plane by π–π inter­actions between their phenyl substituents.