Dichlorobis(di-tert-butylphenylphosphine)palladium(II)
Pd 17.1%
- Product Code: 68438
CAS:
34409-44-4
| Molecular Weight: | 621.95 g./mol | Molecular Formula: | C₂₈H₄₆Cl₂P₂Pd |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09953450 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2~8°C |
Product Description:
This chemical is widely used as a catalyst in various organic synthesis reactions, particularly in cross-coupling reactions such as Suzuki, Heck, and Stille couplings. Its effectiveness in facilitating the formation of carbon-carbon bonds makes it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The sterically bulky di-tert-butylphenylphosphine ligands enhance the stability and selectivity of the palladium center, allowing for efficient catalysis under mild conditions. Additionally, it is employed in the synthesis of complex organic molecules, including natural products and polymers, due to its ability to operate in diverse reaction environments. Its use extends to fine chemical manufacturing and research applications where precise control over reaction outcomes is essential.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | LIGHT YELLOW TO DARK YELLOW POWDER |
| ASSAYPD | 17 |
| INFRARED SPECTRUM | Conforms to Structure |
| PROTON NMR SPECTRUM | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,390.00 |
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| 1.000 | 10-20 days | ฿3,450.00 |
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| 5.000 | 10-20 days | ฿16,020.00 |
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Dichlorobis(di-tert-butylphenylphosphine)palladium(II)
This chemical is widely used as a catalyst in various organic synthesis reactions, particularly in cross-coupling reactions such as Suzuki, Heck, and Stille couplings. Its effectiveness in facilitating the formation of carbon-carbon bonds makes it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The sterically bulky di-tert-butylphenylphosphine ligands enhance the stability and selectivity of the palladium center, allowing for efficient catalysis under mild conditions. Additionally, it is employed in the synthesis of complex organic molecules, including natural products and polymers, due to its ability to operate in diverse reaction environments. Its use extends to fine chemical manufacturing and research applications where precise control over reaction outcomes is essential.
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