(11bS)-2,6-bis[3,5-bis(trifluoromethyl)phenyl]-N,N-bis[(1R)-1-phenylethyl]-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine
97%
- Product Code: 68595
CAS:
1642864-21-8
| Molecular Weight: | 963.79 g./mol | Molecular Formula: | C₅₂H₃₄F₁₂NO₂P |
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| Density: | Storage Condition: | 2-8°C, protected from light, inert gas |
Product Description:
This chemical is primarily utilized in asymmetric catalysis, particularly in enantioselective transformations. Its unique structure, featuring chiral centers and electron-withdrawing trifluoromethyl groups, makes it highly effective in facilitating reactions where precise control over stereochemistry is crucial. It is often employed in the synthesis of complex organic molecules, including pharmaceuticals, where achieving a specific enantiomer is essential for biological activity. Additionally, its robust framework allows it to perform well under various reaction conditions, making it a versatile catalyst in organic synthesis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | $334.56 |
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(11bS)-2,6-bis[3,5-bis(trifluoromethyl)phenyl]-N,N-bis[(1R)-1-phenylethyl]-dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine
This chemical is primarily utilized in asymmetric catalysis, particularly in enantioselective transformations. Its unique structure, featuring chiral centers and electron-withdrawing trifluoromethyl groups, makes it highly effective in facilitating reactions where precise control over stereochemistry is crucial. It is often employed in the synthesis of complex organic molecules, including pharmaceuticals, where achieving a specific enantiomer is essential for biological activity. Additionally, its robust framework allows it to perform well under various reaction conditions, making it a versatile catalyst in organic synthesis.
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