(1,3-Bis(2,6-diisopropylphenyl)-1H-imidazol-2(3H)-ylidene)chloro(cinnamyl)palladate(II)
98%
- Product Code: 61113
CAS:
884879-23-6
| Molecular Weight: | 647.63 g./mol | Molecular Formula: | C₃₆H₄₅ClN₂Pd |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11045095 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, airtight, dry |
Product Description:
This chemical is widely used as a catalyst in various organic synthesis reactions, particularly in cross-coupling processes such as Suzuki-Miyaura and Heck reactions. Its robust structure and stability under reaction conditions make it highly effective for forming carbon-carbon bonds, which are essential in the production of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it is employed in the synthesis of complex organic molecules due to its ability to facilitate challenging transformations with high selectivity and efficiency. Its use in asymmetric catalysis also contributes to the production of enantiomerically pure compounds, which are critical in drug development.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Light yellow to Yellow Powder |
| PURITY | 97.5-100 |
| PALLADIUM PD | 16 17% |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $102.46 |
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| 0.250 | 10-20 days | $181.32 |
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| 1.000 | 10-20 days | $648.92 |
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(1,3-Bis(2,6-diisopropylphenyl)-1H-imidazol-2(3H)-ylidene)chloro(cinnamyl)palladate(II)
This chemical is widely used as a catalyst in various organic synthesis reactions, particularly in cross-coupling processes such as Suzuki-Miyaura and Heck reactions. Its robust structure and stability under reaction conditions make it highly effective for forming carbon-carbon bonds, which are essential in the production of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it is employed in the synthesis of complex organic molecules due to its ability to facilitate challenging transformations with high selectivity and efficiency. Its use in asymmetric catalysis also contributes to the production of enantiomerically pure compounds, which are critical in drug development.
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