Dichlorobis(di-tert-butylphenylphosphine)palladium(II)
99.95% metals basis
- Product Code: 168869
CAS:
34409-44-4
| Molecular Weight: | 621.95 g./mol | Molecular Formula: | C₂₈H₄₆Cl₂P₂Pd |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09953450 | |
| Melting Point: | 260-264 °C | Boiling Point: | |
| Density: | Storage Condition: | -20°C |
Product Description:
Widely used as a palladium-based catalyst in cross-coupling reactions, particularly in Suzuki-Miyaura and Buchwald-Hartwig aminations. Its bulky di-tert-butylphenylphosphine ligands enhance reactivity and stability, allowing efficient coupling of aryl chlorides, which are less reactive than bromides or iodides. This makes it cost-effective and practical for synthesizing complex organic molecules, especially in pharmaceutical and agrochemical industries. The catalyst promotes high yields under mild conditions and is effective with a broad substrate scope, including sterically hindered partners. It is also employed in the formation of carbon–nitrogen and carbon–carbon bonds in advanced intermediate synthesis.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 G | 10-20 days | ฿6,020.00 |
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Dichlorobis(di-tert-butylphenylphosphine)palladium(II)
Widely used as a palladium-based catalyst in cross-coupling reactions, particularly in Suzuki-Miyaura and Buchwald-Hartwig aminations. Its bulky di-tert-butylphenylphosphine ligands enhance reactivity and stability, allowing efficient coupling of aryl chlorides, which are less reactive than bromides or iodides. This makes it cost-effective and practical for synthesizing complex organic molecules, especially in pharmaceutical and agrochemical industries. The catalyst promotes high yields under mild conditions and is effective with a broad substrate scope, including sterically hindered partners. It is also employed in the formation of carbon–nitrogen and carbon–carbon bonds in advanced intermediate synthesis.
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