Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its rigid cyclohexane backbone with functionalized ketone and ester groups allows for selective transformations, making it valuable in constructing complex molecules. Commonly employed in asymmetric synthesis and ring-functionalization reactions to develop biologically active compounds, including steroid analogs and enzyme inhibitors. The presence of the 4-oxo group enables further reduction or nucleophilic addition, while the ester groups can be hydrolyzed or reduced to tailor reactivity. Its trans configuration supports stereoselective pathways in synthetic routes.