Dicyclohexyl(2',4',6'-triisopropyl-3,6-dimethoxy-[1,1'-biphenyl]-2-yl)phosphine-(2-(2-aminoethyl)phenyl)palladium(II) chloride
≥98%
- Product Code: 53240
CAS:
1148148-01-9
| Molecular Weight: | 797.80 g./mol | Molecular Formula: | C₄₃H₆₂ClNO₂PPd |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12545956 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This chemical is primarily used as a highly efficient catalyst in various cross-coupling reactions, particularly in organic synthesis. It plays a crucial role in facilitating the formation of carbon-carbon and carbon-heteroatom bonds, which are essential in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its application is particularly notable in Buchwald-Hartwig amination reactions, where it enables the coupling of aryl halides with amines, leading to the synthesis of complex organic molecules. Additionally, its stability and selectivity make it a preferred choice in the development of novel compounds in medicinal chemistry and material science.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft37,601.64 |
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| 0.250 | 10-20 days | Ft59,796.30 |
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| 1.000 | 10-20 days | Ft140,602.11 |
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| 5.000 | 10-20 days | Ft562,947.14 |
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Dicyclohexyl(2',4',6'-triisopropyl-3,6-dimethoxy-[1,1'-biphenyl]-2-yl)phosphine-(2-(2-aminoethyl)phenyl)palladium(II) chloride
This chemical is primarily used as a highly efficient catalyst in various cross-coupling reactions, particularly in organic synthesis. It plays a crucial role in facilitating the formation of carbon-carbon and carbon-heteroatom bonds, which are essential in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its application is particularly notable in Buchwald-Hartwig amination reactions, where it enables the coupling of aryl halides with amines, leading to the synthesis of complex organic molecules. Additionally, its stability and selectivity make it a preferred choice in the development of novel compounds in medicinal chemistry and material science.
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