Methanesulfonato [2-(Di-1-adamantylphosphino)-2',4',6'-triisopropyl-3,6-dimethoxybiphenyl][2-(2'-amino-1,1'-biphenyl)]palladium(II)
98%
- Product Code: 214297
CAS:
1507404-60-5
| Molecular Weight: | 1065.6 g./mol | Molecular Formula: | C₅₆H₇₂F₃NO₅PPdS+ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD27952546 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
Widely used as a highly active and stable palladium-based catalyst in cross-coupling reactions, particularly in Buchwald–Hartwig amination and Suzuki–Miyaura coupling. Its sterically hindered adamantyl and isopropyl groups enhance catalyst longevity and reactivity, enabling efficient carbon–nitrogen and carbon–carbon bond formation under mild conditions. Commonly applied in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and functional materials, where high selectivity and yield are critical. Performs well with challenging substrates, including aryl chlorides, which are typically less reactive. Often used in low catalyst loadings, reducing costs and metal contamination in final products.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿2,450.00 |
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| 250mg | 10-20 days | ฿4,950.00 |
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Methanesulfonato [2-(Di-1-adamantylphosphino)-2',4',6'-triisopropyl-3,6-dimethoxybiphenyl][2-(2'-amino-1,1'-biphenyl)]palladium(II)
Widely used as a highly active and stable palladium-based catalyst in cross-coupling reactions, particularly in Buchwald–Hartwig amination and Suzuki–Miyaura coupling. Its sterically hindered adamantyl and isopropyl groups enhance catalyst longevity and reactivity, enabling efficient carbon–nitrogen and carbon–carbon bond formation under mild conditions. Commonly applied in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and functional materials, where high selectivity and yield are critical. Performs well with challenging substrates, including aryl chlorides, which are typically less reactive. Often used in low catalyst loadings, reducing costs and metal contamination in final products.
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