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Structure of 1365531-81-2
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(R)-2,2'-Bis(di-p-tolylphosphino)-4,4',6,6'-tetramethoxy-1,1'-biphenyl is a sterically hindered, electron-rich phosphine ligand designed for palladium-catalyzed cross-coupling reactions. The tetramethoxy substitution enhances solubility and stability under reaction conditions, while the chiral biphenyl backbone provides precise control over stereochemistry in asymmetric transformations. This ligand integrates seamlessly into catalytic systems requiring robust performance and high selectivity.
(R)-2,2'-Bis(di-p-tolylphosphino)-4,4',6,6'-tetramethoxy-1,1'-biphenyl serves as a highly functional, bench-stable ligand in palladium-catalyzed cross-coupling reactions. Its electron-rich phosphine centers enable efficient formation of C–C and C–heteroatom bonds under mild conditions. The tetramethoxy substitution enhances solubility and stability, while the steric bulk supports high selectivity in Suzuki-Miyaura and Negishi couplings. Ideal for complex molecule assembly in medicinal chemistry and materials synthesis.
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Lot numbers can be found on the outside label of a product: