Palladium pivalate
98%
- Product Code: 68487
Alias:
Palladium (II) trimethyl acetate; Palladium dipivalate; Palladium (II) pivalate
CAS:
106224-36-6
| Molecular Weight: | 308.67 g./mol | Molecular Formula: | C₁₀H₁₈O₄Pd |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16038138 | |
| Melting Point: | Boiling Point: | 230-232°C | |
| Density: | Storage Condition: | room temperature, in an inert gas |
Product Description:
Palladium pivalate is widely used as a catalyst in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura and Heck reactions. These reactions are essential for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its stability and efficiency make it a preferred choice in industrial and academic research settings. Additionally, it is employed in the preparation of fine chemicals and in the development of new catalytic processes due to its ability to operate under mild conditions and with high selectivity.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Orange to Dark Red to Red-Brown to Brown solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,530.00 |
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| 0.250 | 10-20 days | ฿2,930.00 |
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| 1.000 | 10-20 days | ฿9,440.00 |
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| 5.000 | 10-20 days | ฿44,860.00 |
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Palladium pivalate
Palladium pivalate is widely used as a catalyst in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura and Heck reactions. These reactions are essential for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its stability and efficiency make it a preferred choice in industrial and academic research settings. Additionally, it is employed in the preparation of fine chemicals and in the development of new catalytic processes due to its ability to operate under mild conditions and with high selectivity.
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