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Structure of 12081-18-4
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Bis(2-methylallyl)dipalladium dichloride serves as a robust, bench-stable precursor for palladium-catalyzed cross-coupling reactions. Featuring two 2-methylallyl ligands coordinated to a Pd₂Cl₂ core, it enables efficient C–C and C–heteroatom bond formation under mild conditions. The sterically protected allyl groups enhance reactivity while minimizing decomposition pathways. This complex streamlines catalyst activation in synthetic workflows involving nickel or palladium systems.
Bis(2-methylallyl)dipalladium dichloride serves as a robust, bench-stable precursor for palladium-catalyzed cross-coupling reactions. It enables efficient C–C and C–heteroatom bond formation under mild conditions, demonstrating broad functional group tolerance and compatibility with standard reaction protocols. Its well-defined structure facilitates reproducible catalytic activity in Suzuki-Miyaura, Stille, and Negishi couplings, making it a reliable choice for synthetic chemists constructing complex molecular architectures.
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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-P405-P501
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Lot numbers can be found on the outside label of a product: