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AB54881

12081-18-4 | (2-Methylallyl)palladium(II) chloride dimer

Packsize Purity Availability Price Discounted Price    Quantity
250mg 98% in stock $56.00 $40.00 -   +
1g 98% in stock $159.00 $112.00 -   +

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*All prices are in USD.

Description
Catalog Number: AB54881
Chemical Name: (2-Methylallyl)palladium(II) chloride dimer
CAS Number: 12081-18-4
Molecular Formula: C8H10Cl2Pd2
Molecular Weight: 389.911
MDL Number: MFCD08561141
SMILES: C[C]12=C[Pd+2]32([CH-]1)[Cl-][Pd+2]12([Cl-]3)[CH-][C]2(=C1)C

 

Upstream Synthesis Route
  • Bis(2-methylallyl)palladium chloride dimer, also known as (2-methylallyl)2PdCl2, is a valuable organometallic catalyst widely used in chemical synthesis applications. This complex plays a crucial role in promoting various cross-coupling reactions, particularly in the field of organic chemistry.One of the main applications of this compound is in the Suzuki-Miyaura coupling reaction, a fundamental method for forming carbon-carbon bonds. In this process, the (2-methylallyl)2PdCl2 acts as a catalyst, facilitating the coupling of aryl halides with organoboron reagents. This reaction allows for the efficient construction of complex organic molecules, making it a key tool in medicinal chemistry, materials science, and natural product synthesis.Furthermore, Bis(2-methylallyl)palladium chloride dimer is also utilized in Heck reactions, a versatile transformation that enables the direct arylation of alkenes. By mediating the transfer of aryl groups onto double bonds, this catalyst enables the rapid and selective formation of valuable carbon-carbon bonds, expanding the synthetic possibilities for organic chemists.Overall, the application of Bis(2-methylallyl)palladium chloride dimer in chemical synthesis offers a powerful and efficient method for the construction of intricate molecular structures, making it an indispensable resource for researchers and practitioners in the field of organic chemistry.
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