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Structure of 478980-01-7
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This palladium(II) complex features a sterically shielded, electron-rich N-heterocyclic carbene ligand that enhances stability and reactivity in cross-coupling catalysis. The allyl group enables facile transmetalation, while the bulky 2,6-diisopropylphenyl substituents prevent catalyst deactivation. Ideal for C–C bond formation under mild conditions.
Allyl(1,3-bis(2,6-diisopropylphenyl)imidazolidin-2-ylidene)chloropalladate(II) serves as a highly stable, bench-ready palladium catalyst precursor for cross-coupling reactions. Its sterically shielded N-heterocyclic carbene ligand enhances reactivity and tolerance to diverse functional groups, enabling efficient Suzuki-Miyaura, Stille, and Negishi couplings. The complex facilitates catalytic turnover under mild conditions with minimal Pd aggregation, making it well-suited for scalable synthesis and iterative molecular construction in medicinal chemistry workflows.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H315-H319-H335
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Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: