Dichloro[(S)-2,2-bis(diphenylphosphino)-1,1-binaphthyl]palladium(II)
97%
- Product Code: 68343
CAS:
127593-28-6
Molecular Weight: | 800.00 g./mol | Molecular Formula: | C₄₄H₃₂Cl₂P₂Pd |
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EC Number: | MDL Number: | MFCD00075254 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
This chemical is widely used as a catalyst in various organic synthesis reactions, particularly in asymmetric catalysis. It plays a key role in cross-coupling reactions, such as the Suzuki-Miyaura and Heck reactions, enabling the formation of carbon-carbon bonds with high enantioselectivity. Its application is crucial in the pharmaceutical industry for the synthesis of chiral compounds, which are essential in the production of active pharmaceutical ingredients (APIs). Additionally, it is utilized in the development of advanced materials and fine chemicals, where precise control over molecular structure and stereochemistry is required. Its effectiveness in promoting complex transformations makes it a valuable tool in modern synthetic chemistry.
Product Specification:
Test | Specification |
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APPEARANCE | 96.5-100 |
PURITY | Red Solid |
Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿1,470.00 |
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1.000 | 10-20 days | ฿4,210.00 |
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Dichloro[(S)-2,2-bis(diphenylphosphino)-1,1-binaphthyl]palladium(II)
This chemical is widely used as a catalyst in various organic synthesis reactions, particularly in asymmetric catalysis. It plays a key role in cross-coupling reactions, such as the Suzuki-Miyaura and Heck reactions, enabling the formation of carbon-carbon bonds with high enantioselectivity. Its application is crucial in the pharmaceutical industry for the synthesis of chiral compounds, which are essential in the production of active pharmaceutical ingredients (APIs). Additionally, it is utilized in the development of advanced materials and fine chemicals, where precise control over molecular structure and stereochemistry is required. Its effectiveness in promoting complex transformations makes it a valuable tool in modern synthetic chemistry.
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