(R)-3,3'-Bis[3,5-bis(trifluoromethyl)phenyl]-5,5',6,6',7,7',8,8'-octahydro-1,1'-bi-2,2'-naphthol
≥98%,99%e.e.
- Product Code: 70326
CAS:
618854-91-4
| Molecular Weight: | 718.6 g./mol | Molecular Formula: | C₃₆H₂₆F₁₂O₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | 195-196°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. Its unique structure, featuring trifluoromethyl groups and a rigid binaphthol backbone, makes it highly effective in enantioselective reactions, particularly in the formation of chiral centers in organic molecules. It is often employed in transition-metal-catalyzed processes, such as hydrogenation, carbon-carbon bond formation, and other transformations requiring high enantiomeric excess. Additionally, its electron-withdrawing trifluoromethyl groups enhance its stability and reactivity in challenging chemical environments, making it a valuable tool in pharmaceutical and fine chemical synthesis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,820.00 |
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| 0.250 | 10-20 days | ฿6,550.00 |
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(R)-3,3'-Bis[3,5-bis(trifluoromethyl)phenyl]-5,5',6,6',7,7',8,8'-octahydro-1,1'-bi-2,2'-naphthol
This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. Its unique structure, featuring trifluoromethyl groups and a rigid binaphthol backbone, makes it highly effective in enantioselective reactions, particularly in the formation of chiral centers in organic molecules. It is often employed in transition-metal-catalyzed processes, such as hydrogenation, carbon-carbon bond formation, and other transformations requiring high enantiomeric excess. Additionally, its electron-withdrawing trifluoromethyl groups enhance its stability and reactivity in challenging chemical environments, making it a valuable tool in pharmaceutical and fine chemical synthesis.
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