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DICHLOROBIS(TRI-O-TOLYLPHOSPHINE)PALLADIUM(II) CAS:40691-33-6

DICHLOROBIS(TRI-O-TOLYLPHOSPHINE)PALLADIUM(II) is a coordination complex consisting of palladium coordinated with tri-o-tolylphosphine ligands and chloride ligands. It is recognized for its applications in catalysis and organic synthesis.


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Application and Effect:

DICHLOROBIS(TRI-O-TOLYLPHOSPHINE)PALLADIUM(II) serves as a catalyst in various organic transformations. One significant application is in palladium-catalyzed cross-coupling reactions, such as the Suzuki-Miyaura coupling and the Heck reaction. In these reactions, it facilitates the formation of carbon-carbon bonds between organic substrates, enabling the synthesis of complex molecules with high efficiency and selectivity. These reactions find widespread use in the synthesis of pharmaceuticals, agrochemicals, and materials. Moreover, the complex is employed in C-H activation reactions, enabling the functionalization of unreactive C-H bonds in organic compounds. This transformation allows for the direct formation of new bonds, streamlining synthetic routes and minimizing waste. Additionally, DICHLOROBIS(TRI-O-TOLYLPHOSPHINE)PALLADIUM(II) finds applications in the synthesis of heterocyclic compounds via palladium-catalyzed cyclization reactions. These reactions enable the construction of diverse heterocycles, which are prevalent in pharmaceuticals, agrochemicals, and materials science. Furthermore, the complex is utilized in the preparation of vinylsilanes through palladium-catalyzed silylation reactions. Vinylsilanes are versatile intermediates in organic synthesis, participating in cross-coupling reactions, cycloadditions, and other transformations. Moreover, DICHLOROBIS(TRI-O-TOLYLPHOSPHINE)PALLADIUM(II) is employed in carbonylation reactions, enabling the conversion of aryl halides to aryl ketones or esters. This process is important in the synthesis of fine chemicals, pharmaceuticals, and polymers. Additionally, the complex serves as a catalyst in palladium-catalyzed allylic substitutions, facilitating the substitution of allylic substrates with nucleophiles to form allylic products with high regio- and stereo-selectivity. These reactions are valuable in the synthesis of chiral building blocks and natural products. In summary, DICHLOROBIS(TRI-O-TOLYLPHOSPHINE)PALLADIUM(II) is a versatile catalyst employed in cross-coupling reactions, C-H activation, cyclization, silylation, carbonylation, and allylic substitutions. Its applications span from the synthesis of pharmaceuticals and agrochemicals to the functionalization of organic molecules, making it a valuable tool in organic synthesis and catalysis.

Product Sample:

Amino acid powder1
Amino acid powder2

Product Packing:

Amino acid powder3
Amino acid powder4
Amino acid powder5
Amino acid powder6

Additional Information:

Composition C42H44Cl2P2Pd
Assay 99%
Appearance white powder
CAS No.  40691-33-6
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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