(4S,5S)-4,5-Diphenyl-2-(quinolin-2-yl)-4,5-dihydrooxazole
98%
- Product Code: 37013
CAS:
2058236-55-6
| Molecular Weight: | 350.4100 g./mol | Molecular Formula: | C₂₄H₁₈N₂O |
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| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in enantioselective reactions. Its chiral structure makes it valuable as a ligand in transition metal-catalyzed processes, such as hydrogenation, allylic alkylation, and C–C bond-forming reactions. The presence of the quinoline moiety enhances its coordination ability with metals, improving catalytic efficiency and selectivity. Additionally, it is employed in the development of chiral catalysts for pharmaceutical synthesis, where high enantiomeric purity is crucial. Its application extends to organic synthesis research, aiding in the production of complex molecules with precise stereochemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,085.00 |
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(4S,5S)-4,5-Diphenyl-2-(quinolin-2-yl)-4,5-dihydrooxazole
This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in enantioselective reactions. Its chiral structure makes it valuable as a ligand in transition metal-catalyzed processes, such as hydrogenation, allylic alkylation, and C–C bond-forming reactions. The presence of the quinoline moiety enhances its coordination ability with metals, improving catalytic efficiency and selectivity. Additionally, it is employed in the development of chiral catalysts for pharmaceutical synthesis, where high enantiomeric purity is crucial. Its application extends to organic synthesis research, aiding in the production of complex molecules with precise stereochemistry.
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