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In the asymmetric unit of the title compound, C 38 H 56 O 3 , there are two symmetry-independent mol­ecules that differ in the rotation angle along the C—O bond between the 3-(4-eth­oxy­phen­yl)prop-2-enoate and cholest-5-en-3β-yl groups by 169.3 (3)°. In both mol­ecules, steroid ring  B  adopts a half-chair conformation, rings  A  and  C  adopt a chair conformation and ring  D  exists in an envelope form. The two symmetry-independent mol­ecules pack in the crystal into separate layers parallel to (-102) with their long axis parallel to the [201] direction. Short inter­molecular C—H⋯O and C—H⋯π contacts are observed.

Cholest-5-en-3β-yl 3-(4-ethoxyphenyl)prop-2-enoate