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Dibromobis(tri-ortho-tolyphosphine)palladium(II) CAS:24554-43-6

Dibromobis(tri-ortho-tolyphosphine)palladium(II) is a coordination complex featuring palladium(II) as the central metal atom, coordinated with two bromide ligands and two tri-ortho-tolyphosphine ligands. It is renowned for its significance in various catalytic processes due to its distinctive structure and reactivity.


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Application and Effect:

Dibromobis(tri-ortho-tolyphosphine)palladium(II) holds pivotal roles across multiple chemical transformations and industries, owing to its exceptional catalytic attributes. Here are its primary applications: Cross-Coupling Reactions: Widely utilized as a catalyst in cross-coupling reactions, Dibromobis(tri-ortho-tolyphosphine)palladium(II) facilitates the formation of carbon-carbon bonds, crucial for the synthesis of complex organic molecules such as pharmaceuticals, agrochemicals, and materials. Heck Reaction: It plays a vital role in the Heck reaction, enabling the coupling of aryl halides with olefins to yield functionalized alkenes. This transformation is significant in organic synthesis for the preparation of various industrially relevant compounds. Suzuki Coupling: As a catalyst in Suzuki coupling reactions, it enables the cross-coupling of aryl or vinyl halides with boronic acids or boronates, leading to the formation of biaryl compounds. This reaction has widespread applications in pharmaceuticals, materials science, and agrochemicals. Sonogashira Coupling: Dibromobis(tri-ortho-tolyphosphine)palladium(II) facilitates Sonogashira coupling reactions, allowing the synthesis of alkynes from aryl or vinyl halides with terminal alkynes. This transformation is crucial in the preparation of conjugated systems and natural product synthesis. C–H Activation: It promotes C–H activation reactions, enabling the functionalization of unactivated carbon-hydrogen bonds to introduce new functionalities. This strategy offers efficient routes to access complex molecules and streamline synthesis processes. Allylic Substitution: As a catalyst in allylic substitution reactions, it enables the substitution of allylic electrophiles with nucleophiles, facilitating the synthesis of diverse organic compounds with high regio- and stereo-selectivity. Dibromobis(tri-ortho-tolyphosphine)palladium(II) stands as a versatile and indispensable catalyst in modern synthetic chemistry, driving advancements in organic synthesis and facilitating the creation of intricate molecular architectures across various industrial sectors. Its applications encompass pharmaceuticals, materials science, agrochemicals, and beyond, contributing to the innovation and advancement of chemical synthesis methodologies.

Product Sample:

L-Arginine1
L-Arginine2

Product Packing:

L-Arginin3

Additional Information:

Composition C42H42Br2P2Pd
Assay 99%
Appearance white powder
CAS No.  24554-43-6
Packing Small and bulk
Shelf Life 2 years
Storage Store in cool and dry area
Certification ISO.

 


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