6,6'-Bis((S)-4-benzyl-4,5-dihydrooxazol-2-yl)-2,2'-bipyridine
95%
- Product Code: 49372
CAS:
2088982-18-5
| Molecular Weight: | 474.5500 g./mol | Molecular Formula: | C₃₀H₂₆N₄O₂ |
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| EC Number: | MDL Number: | MFCD00009593 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis. It is highly effective in facilitating asymmetric hydrogenation, a process critical for producing chiral molecules in pharmaceuticals and fine chemicals. Its rigid bipyridine core, combined with chiral oxazoline moieties, allows for precise control over stereochemistry, making it valuable in the synthesis of complex organic compounds with high enantiomeric purity. Additionally, it is employed in the development of advanced materials, such as chiral polymers or metal-organic frameworks, where its structural properties enhance selectivity and functionality. Its application extends to academic research, where it serves as a model ligand for studying asymmetric induction and catalytic mechanisms.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,194.00 |
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| 0.250 | 10-20 days | ฿8,820.00 |
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| 1.000 | 10-20 days | ฿26,730.00 |
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6,6'-Bis((S)-4-benzyl-4,5-dihydrooxazol-2-yl)-2,2'-bipyridine
This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis. It is highly effective in facilitating asymmetric hydrogenation, a process critical for producing chiral molecules in pharmaceuticals and fine chemicals. Its rigid bipyridine core, combined with chiral oxazoline moieties, allows for precise control over stereochemistry, making it valuable in the synthesis of complex organic compounds with high enantiomeric purity. Additionally, it is employed in the development of advanced materials, such as chiral polymers or metal-organic frameworks, where its structural properties enhance selectivity and functionality. Its application extends to academic research, where it serves as a model ligand for studying asymmetric induction and catalytic mechanisms.
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