(2R,3R)-(-)-2,3-Bis(diphenylphosphino)bicyclo[2.2.1]hept-5-ene
98.0%
- Product Code: 68613
CAS:
71042-55-2
| Molecular Weight: | 462.51 g./mol | Molecular Formula: | C₃₁H₂₈P₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00085365 | |
| Melting Point: | 120-125 °C | Boiling Point: | |
| Density: | Storage Condition: | 2~8°C |
Product Description:
This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in transition metal-catalyzed reactions. Its unique bicyclic structure and chiral centers make it highly effective in inducing enantioselectivity in various organic transformations. It is commonly employed in hydrogenation reactions, where it helps produce chiral compounds with high optical purity. Additionally, it finds application in cross-coupling reactions, such as the Suzuki-Miyaura and Heck reactions, to synthesize complex molecules with specific stereochemistry. Its role in catalysis is crucial for the production of pharmaceuticals, agrochemicals, and fine chemicals, where precise control over stereochemistry is essential.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White - Almost white Crystal - Powder |
| PURITY | 98-100 |
| Specific rotation a20Dc1 CHCl3 | -51--45 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,941.00 |
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| 0.250 | 10-20 days | ฿11,952.00 |
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| 1.000 | 10-20 days | ฿24,912.00 |
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(2R,3R)-(-)-2,3-Bis(diphenylphosphino)bicyclo[2.2.1]hept-5-ene
This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in transition metal-catalyzed reactions. Its unique bicyclic structure and chiral centers make it highly effective in inducing enantioselectivity in various organic transformations. It is commonly employed in hydrogenation reactions, where it helps produce chiral compounds with high optical purity. Additionally, it finds application in cross-coupling reactions, such as the Suzuki-Miyaura and Heck reactions, to synthesize complex molecules with specific stereochemistry. Its role in catalysis is crucial for the production of pharmaceuticals, agrochemicals, and fine chemicals, where precise control over stereochemistry is essential.
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