(SP-4-2)-[1,3-Bis[2,6-bis(1-methylethyl)phenyl]-1,3-dihydro-2H-imidazol-2-ylidene]chloro(2,4-pentanedionato-κO2,κO4)palladium
98%
- Product Code: 237038
CAS:
868705-03-7
| Molecular Weight: | 629.570 g./mol | Molecular Formula: | C₃₂H₄₃ClN₂O₂Pd |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, light-proof, inert gas |
Product Description:
Widely used as a precatalyst in cross-coupling reactions, this palladium complex is particularly effective in carbon–carbon and carbon–heteroatom bond formations. It shows high activity and stability under a variety of reaction conditions, making it suitable for industrial and academic applications. Commonly employed in Suzuki–Miyaura, Heck, and Negishi couplings, it facilitates the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and functional materials. The bulky N-heterocyclic carbene ligand enhances catalyst longevity and turnover, even at low catalyst loadings. It performs well in both aerobic and moisture-tolerant environments, reducing the need for stringent reaction conditions. Its solubility in common organic solvents allows for broad compatibility in reaction setups.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿7,950.00 |
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| 1g | 10-20 days | ฿15,990.00 |
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(SP-4-2)-[1,3-Bis[2,6-bis(1-methylethyl)phenyl]-1,3-dihydro-2H-imidazol-2-ylidene]chloro(2,4-pentanedionato-κO2,κO4)palladium
Widely used as a precatalyst in cross-coupling reactions, this palladium complex is particularly effective in carbon–carbon and carbon–heteroatom bond formations. It shows high activity and stability under a variety of reaction conditions, making it suitable for industrial and academic applications. Commonly employed in Suzuki–Miyaura, Heck, and Negishi couplings, it facilitates the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and functional materials. The bulky N-heterocyclic carbene ligand enhances catalyst longevity and turnover, even at low catalyst loadings. It performs well in both aerobic and moisture-tolerant environments, reducing the need for stringent reaction conditions. Its solubility in common organic solvents allows for broad compatibility in reaction setups.
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