Molecular Weight
1172.24
Molecular Formula
C78H65ClN2Pd
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- Chloro[(1,2,3-η)-1-phenyl-2-propen-1-yl]-{[1,3-bis[2,6-bis(diphenylmethyl)-4-methylphenyl]-2H-imidazol-2-ylidene}palladium(II), min. 97%
Chloro[(1,2,3-η)-1-phenyl-2-propen-1-yl]-{[1,3-bis[2,6-bis(diphenylmethyl)-4-methylphenyl]-2H-imidazol-2-ylidene}palladium(II), min. 97%
Catalog Number
ACM1380314248
Product Name
Chloro[(1,2,3-η)-1-phenyl-2-propen-1-yl]-{[1,3-bis[2,6-bis(diphenylmethyl)-4-methylphenyl]-2H-imidazol-2-ylidene}palladium(II), min. 97%
Structure
![{[CurrentData.Name]}](https://resource.alfachemic.com/structure/1380314-24-8.gif)
CAS
1380314-24-8
Application
The compound Chloro[(1,2,3-η)-1-phenyl-2-propen-1-yl]-{[1,3-bis[2,6-bis(diphenylmethyl)-4-methylphenyl]-2H-imidazol-2-ylidene}palladium(II), with a minimum purity of 97%, serves as a highly efficient homogeneous catalyst tailored for facilitating a variety of important chemical transformations. It is particularly beneficial in cross-coupling reactions involving arenes, enabling processes such as arylation, the Buchwald-Hartwig amination, and Suzuki-Miyaura coupling. This catalyst is instrumental in the Buchwald-Hartwig cross-coupling of aryl compounds, promoting the efficient synthesis of tetra-ortho-substituted biaryls through Suzuki-Miyaura cross-coupling techniques. Additionally, it supports the direct S-arylation of unactivated arylsulfoxides, thus demonstrating its versatility and effectiveness in complex organic syntheses.
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