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Structure of 1798782-11-2
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This palladium complex features a sterically hindered, electron-rich phosphine ligand that enhances catalytic stability and reactivity in cross-coupling processes. Designed for efficient C–C bond formation under mild conditions, it combines robustness with high turnover in challenging transformations.
This palladium complex serves as a highly effective, bench-stable catalyst for cross-coupling reactions, enabling efficient C–C bond formation under mild conditions. Its sterically encumbered dicyclohexylphosphine ligand with extended aryl substitution enhances stability and selectivity, while the trifluoromethanesulfonate counterion facilitates rapid transmetalation. Ideal for Suzuki-Miyaura and Negishi couplings involving sensitive substrates, it offers broad functional group tolerance and simplifies purification in synthetic workflows.
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Lot numbers can be found on the outside label of a product: