(4R,4'R)-4,4'-Di((S)-sec-butyl)-4,4',5,5'-tetrahydro-2,2'-bioxazole
98%
- Product Code: 36969
CAS:
2270178-41-9
| Molecular Weight: | 252.3526 g./mol | Molecular Formula: | C₁₄H₂₄N₂O₂ |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. Its unique structure, featuring bioxazole rings and sec-butyl groups, makes it highly effective in enantioselective reactions, such as hydrogenation, allylic alkylation, and cross-coupling reactions. It is also employed in the synthesis of biologically active molecules and pharmaceuticals, where precise control over stereochemistry is crucial. Additionally, it serves as a building block in organic synthesis for constructing complex molecular architectures with high stereochemical fidelity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,992.00 |
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(4R,4'R)-4,4'-Di((S)-sec-butyl)-4,4',5,5'-tetrahydro-2,2'-bioxazole
This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. Its unique structure, featuring bioxazole rings and sec-butyl groups, makes it highly effective in enantioselective reactions, such as hydrogenation, allylic alkylation, and cross-coupling reactions. It is also employed in the synthesis of biologically active molecules and pharmaceuticals, where precise control over stereochemistry is crucial. Additionally, it serves as a building block in organic synthesis for constructing complex molecular architectures with high stereochemical fidelity.
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