(4S,4'S)-2,2'-(oxybis(2,1-phenylene))bis(4-phenyl-4,5-dihydrooxazole)

• CAT Number: L002390
• CAS Number: 1613706-51-6
• Molecular Formula: C30H24N2O3
• Molecular Weight: 460.51
• Purity: ≥95%
• IUPAC Name: (4S)-4-phenyl-2-[2-[2-[(4S)-4-phenyl-4,5-dihydro-1,3-oxazol-2-yl]phenoxy]phenyl]-4,5-dihydro-1,3-oxazole
• InChI: InChI=1S/C30H24N2O3/c1-3-11-21(12-4-1)25-19-33-29(31-25)23-15-7-9-17-27(23)35-28-18-10-8-16-24(28)30-32-26(20-34-30)22-13-5-2-6-14-22/h1-18,25-26H,19-20H2/t25-,26-/m1/s1
• InChIKey: WBBKXXKVLURHRH-CLJLJLNGSA-N
• SMILES: C1[C@@H](N=C(O1)C2=CC=CC=C2OC3=CC=CC=C3C4=N[C@H](CO4)C5=CC=CC=C5)C6=CC=CC=C6

(4S,4’S)-2,2′-(Oxybis(2,1-phenylene))bis(4-phenyl-4,5-dihydrooxazole)(CAT: L002390) is a high-purity chiral bis-oxazoline compound widely used in asymmetric synthesis and catalytic applications. Featuring two dihydrooxazole rings linked through a phenylene ether backbone, this compound is particularly valuable as a ligand in enantioselective catalytic processes, including cycloaddition, hydrogenation, and cross-coupling reactions. Its well-defined chiral structure enables precise control over stereoselectivity in chemical transformations, making it an essential tool in pharmaceutical research and fine chemical synthesis. (4S,4’S)-2,2′-(Oxybis(2,1-phenylene))bis(4-phenyl-4,5-dihydrooxazole) ensures exceptional stability, reliability, and performance in advanced research and innovative synthetic applications.