(SP-4-1)-[1,3-BIs[2,6-bis(1-ethylpropyl)phenyl]-4,5-dichloro-1,3-dihydro-2H-imidazol-2-ylidene]dichloro(2-methylpyridine)palladium
98%
- Product Code: 237442
CAS:
1612891-29-8
| Molecular Weight: | 840.14 g./mol | Molecular Formula: | C₄₁H₅₇Cl₄N₃Pd |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, Sealed, Dry, Light-proof, Inert Gas |
Product Description:
Widely used as a highly efficient catalyst in cross-coupling reactions, particularly in Suzuki-Miyaura and Buchwald-Hartwig aminations. Its robust structure allows for excellent activity with aryl chlorides, which are typically less reactive, enabling cost-effective and scalable synthetic routes in pharmaceutical and agrochemical manufacturing. The ligand environment enhances palladium stability and prevents premature decomposition, leading to lower catalyst loadings and higher yields. Commonly applied in the formation of C–C and C–N bonds for complex molecule assembly, including drug intermediates and functional materials. Performs well under mild conditions and is compatible with a variety of functional groups, making it a preferred choice in modern synthetic methodologies.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
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| 100mg | 10-20 days | $542.66 |
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| 500mg | 10-20 days | $1,356.65 |
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| 1g | 10-20 days | $2,034.97 |
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| 250mg | 10-20 days | $813.99 |
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(SP-4-1)-[1,3-BIs[2,6-bis(1-ethylpropyl)phenyl]-4,5-dichloro-1,3-dihydro-2H-imidazol-2-ylidene]dichloro(2-methylpyridine)palladium
Widely used as a highly efficient catalyst in cross-coupling reactions, particularly in Suzuki-Miyaura and Buchwald-Hartwig aminations. Its robust structure allows for excellent activity with aryl chlorides, which are typically less reactive, enabling cost-effective and scalable synthetic routes in pharmaceutical and agrochemical manufacturing. The ligand environment enhances palladium stability and prevents premature decomposition, leading to lower catalyst loadings and higher yields. Commonly applied in the formation of C–C and C–N bonds for complex molecule assembly, including drug intermediates and functional materials. Performs well under mild conditions and is compatible with a variety of functional groups, making it a preferred choice in modern synthetic methodologies.
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