(2'-Amino-[1,1'-biphenyl]-2-yl)(dicyclohexyl(2',6'-diisopropoxy-[1,1'-biphenyl]-2-yl)phosphoranyl)palladium(III) chloride

• CAT Number: L031813
• CAS Number: 1375325-68-0
• Molecular Formula: C42H54ClNO2PPd+
• Molecular Weight: 777.71
• Purity: ≥95%
• IUPAC Name: dicyclohexyl-[2-[2,6-di(propan-2-yloxy)phenyl]phenyl]phosphanium;palladium(2+);2-phenylaniline;chloride
• InChI: InChI=1S/C30H43O2P.C12H10N.ClH.Pd/c1-22(2)31-27-19-13-20-28(32-23(3)4)30(27)26-18-11-12-21-29(26)33(24-14-7-5-8-15-24)25-16-9-6-10-17-25;13-12-9-5-4-8-11(12)10-6-2-1-3-7-10;;/h11-13,18-25H,5-10,14-17H2,1-4H3;1-6,8-9H,13H2;1H;/q;-1;;+2
• InChIKey: NVVXJVMOIGXUGC-UHFFFAOYSA-N
• SMILES: CC(C)OC1=C(C(=CC=C1)OC(C)C)C2=CC=CC=C2[PH+](C3CCCCC3)C4CCCCC4.C1=CC=C([C-]=C1)C2=CC=CC=C2N.[Cl-].[Pd+2]

(2′-Amino-[1,1′-biphenyl]-2-yl)(dicyclohexyl(2′,6′-diisopropoxy-[1,1′-biphenyl]-2-yl)phosphoranyl)palladium(III) chloride(CAT: L031813) is a highly active, sterically hindered palladium complex engineered for advanced cross-coupling catalysis. Its unique combination of a biaryl amine and a bulky electron-rich phosphine ligand enhances reactivity and selectivity in C–N, C–C, and C–O bond-forming reactions. This air-stable, pre-activated complex enables efficient transformations under mild conditions, including Buchwald–Hartwig aminations and Suzuki couplings. Its structure supports challenging substrate activation while minimizing side reactions. Widely used in pharmaceutical research and complex molecule synthesis, this complex offers reliable performance in both academic and industrial synthetic workflows requiring high catalytic precision and functional group tolerance.