Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations such as alkylations, aldol reactions, and cycloadditions. Its rigid bis(oxazoline) structure coordinates with metal centers like copper, nickel, or palladium to form highly selective catalysts. Widely employed in pharmaceutical synthesis and fine chemical manufacturing to control stereochemistry and produce single-enantiomer compounds. Soluble in common organic solvents, it enables homogeneous reaction conditions and is valued for high enantiomeric excess in product formation.