(4S,4'S)-2,2'-(Cyclobutane-1,1-diyl)bis(4-phenyl-4,5-dihydrooxazole)
97%
- Product Code: 233401
CAS:
2634687-55-9
| Molecular Weight: | 346.42 g./mol | Molecular Formula: | C₂₂H₂₂N₂O₂ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 499.6±45.0 °C(Predicted) | |
| Density: | 1.27±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, Sealed, Inert Gas |
Product Description:
Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid cyclobutane core and oxazoline rings provide a well-defined chiral environment, making it effective in coordinating to metal centers such as copper or palladium. This complexation enables high enantioselectivity in reactions like cyclopropanations, aldol additions, and Diels-Alder reactions. Due to its stereochemical stability and tunable substituents, it is favored in the synthesis of optically active pharmaceuticals and fine chemicals where precise stereocontrol is critical.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £124.78 |
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(4S,4'S)-2,2'-(Cyclobutane-1,1-diyl)bis(4-phenyl-4,5-dihydrooxazole)
Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid cyclobutane core and oxazoline rings provide a well-defined chiral environment, making it effective in coordinating to metal centers such as copper or palladium. This complexation enables high enantioselectivity in reactions like cyclopropanations, aldol additions, and Diels-Alder reactions. Due to its stereochemical stability and tunable substituents, it is favored in the synthesis of optically active pharmaceuticals and fine chemicals where precise stereocontrol is critical.
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