(4S,4'S)-2,2'-(1,3-Bis(4-(tert-butyl)phenyl)propane-2,2-diyl)bis(4-isopropyl-4,5-dihydrooxazole)

• CAT Number: L003004
• CAS Number: 1373357-05-1
• Molecular Formula: C35H50N2O2
• Molecular Weight: 530.81
• Purity: ≥95%
• IUPAC Name: (4S)-2-[1,3-bis(4-tert-butylphenyl)-2-[(4S)-4-propan-2-yl-4,5-dihydro-1,3-oxazol-2-yl]propan-2-yl]-4-propan-2-yl-4,5-dihydro-1,3-oxazole
• InChI: InChI=1S/C35H50N2O2/c1-23(2)29-21-38-31(36-29)35(32-37-30(22-39-32)24(3)4,19-25-11-15-27(16-12-25)33(5,6)7)20-26-13-17-28(18-14-26)34(8,9)10/h11-18,23-24,29-30H,19-22H2,1-10H3/t29-,30-/m1/s1
• InChIKey: CAJRTABDQGWKNP-LOYHVIPDSA-N

(4S,4’S)-2,2′-(1,3-Bis(4-(tert-butyl)phenyl)propane-2,2-diyl)bis(4-isopropyl-4,5-dihydrooxazole)(CAT: L003004) is a complex chiral compound featuring oxazole rings linked to a central propane structure, substituted with tert-butyl and isopropyl groups. This molecule’s stereochemistry and multiple functional groups make it a valuable ligand and chiral auxiliary in asymmetric synthesis and catalytic reactions. The presence of tert-butyl groups enhances its stability, while the dihydrooxazole rings contribute to its reactivity, particularly in the formation of enantioselective complexes. This compound is utilized in pharmaceutical and chemical research for applications in enantioselective catalysis, where precise stereocontrol is critical for synthesizing optically pure bioactive molecules.