(4S,4'S)-2,2'-(1,3-Bis(4-(tert-butyl)phenyl)propane-2,2-diyl)bis(4-benzyl-4,5-dihydrooxazole)
97%
- Product Code: 36985
CAS:
2172801-78-2
| Molecular Weight: | 626.8693 g./mol | Molecular Formula: | C₄₃H₅₀N₂O₂ |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce chiral molecules with high enantiomeric purity. Its structure, featuring oxazoline rings and bulky tert-butyl groups, enhances its ability to induce asymmetry in reactions. This makes it valuable in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals where specific stereochemistry is required. Additionally, its stability and efficiency in catalytic systems contribute to its widespread use in academic and industrial research for developing enantioselective methodologies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,726.00 |
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(4S,4'S)-2,2'-(1,3-Bis(4-(tert-butyl)phenyl)propane-2,2-diyl)bis(4-benzyl-4,5-dihydrooxazole)
This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce chiral molecules with high enantiomeric purity. Its structure, featuring oxazoline rings and bulky tert-butyl groups, enhances its ability to induce asymmetry in reactions. This makes it valuable in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals where specific stereochemistry is required. Additionally, its stability and efficiency in catalytic systems contribute to its widespread use in academic and industrial research for developing enantioselective methodologies.
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