2,6-Bis[(4S)-benzyl-2-oxazolin-2-yl]pyridine
97%
- Product Code: 70605
CAS:
151670-69-8
| Molecular Weight: | 397.5 g./mol | Molecular Formula: | C₂₅H₂₃N₃O₂ |
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| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, allylic alkylation, and cyclopropanation. Its unique structure allows it to coordinate with transition metals, forming complexes that enhance the stereochemical control of reactions. This makes it valuable in the production of pharmaceuticals, where achieving specific enantiomers is crucial for drug efficacy and safety. Additionally, it is employed in the synthesis of fine chemicals and advanced materials, where precise stereochemistry is required. Its application extends to academic research, where it serves as a tool for developing new catalytic methodologies.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white Solid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿750.00 |
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| 0.500 | 10-20 days | ฿3,530.00 |
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2,6-Bis[(4S)-benzyl-2-oxazolin-2-yl]pyridine
This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, allylic alkylation, and cyclopropanation. Its unique structure allows it to coordinate with transition metals, forming complexes that enhance the stereochemical control of reactions. This makes it valuable in the production of pharmaceuticals, where achieving specific enantiomers is crucial for drug efficacy and safety. Additionally, it is employed in the synthesis of fine chemicals and advanced materials, where precise stereochemistry is required. Its application extends to academic research, where it serves as a tool for developing new catalytic methodologies.
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