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Dichlorobis(methyldiphenylphosphine)palladium(II)

Catalog Number
ACM52611082
Product Name
Dichlorobis(methyldiphenylphosphine)palladium(II)
Structure
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CAS
52611-08-2
  • Product Overview
  • Usage
Synonyms
Bis(methyldiphenylphosphine)palladium(II) dichloride
IUPAC Name
dichloropalladium;methyl(diphenyl)phosphane;
Molecular Weight
577.8
Molecular Formula
C26H26Cl2P2Pd
Canonical SMILES
CP(C1=CC=CC=C1)C2=CC=CC=C2.CP(C1=CC=CC=C1)C2=CC=CC=C2.Cl[Pd]Cl
InChI
InChI=1S/2C13H13P.2ClH.Pd/c2*1-14(12-8-4-2-5-9-12)13-10-6-3-7-11-13;/h2*2-11H,1H3;2*1H;/q;+2/p-2
InChI Key
GTSFBKGHQLDFHU-UHFFFAOYSA-L
Purity
96%
Complexity
139
Covalently-Bonded Unit Count
3
Exact Mass
575.99216
Heavy Atom Count
31
Monoisotopic Mass
575.99216
Rotatable Bond Count
4
Topological Polar Surface Area
0 Ų
Application
Dichlorobis(methyldiphenylphosphine)palladium(II) serves as a catalyst with a primary purpose of facilitating a range of chemical reactions. It is particularly effective in promoting Ullmann reactions, also known as homocoupling reactions, which are essential in forming biaryl compounds. Additionally, this catalyst plays a vital role in the cross coupling reactions between tributyltin hydride and aryl iodides, enabling the formation of various functionalized products. Furthermore, it is utilized in double silylation, double carbonylation, and cyclocarbonylation reactions, providing versatile pathways for synthesizing complex molecular structures. Through these applications, Dichlorobis(methyldiphenylphosphine)palladium(II) supports significant advancements in organic synthesis and material development.
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