(4S)-4-(sec-Butyl)-2-(pyridin-2-yl)-4, 5-dihydrooxazole
98%
- Product Code: 236531
CAS:
1620588-66-0
| Molecular Weight: | 204.27 g./mol | Molecular Formula: | C₁₂H₁₆N₂O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD34563669 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, light-proof |
Product Description:
Used as a chiral auxiliary in asymmetric synthesis, enabling the formation of enantiomerically enriched compounds. Its oxazoline core coordinates effectively with metal catalysts, making it valuable in catalytic asymmetric reactions such as aldol additions, alkylations, and Diels-Alder reactions. Commonly employed in pharmaceutical synthesis where stereochemical control is critical. The sec-butyl group enhances stereoselectivity due to its steric bulk, improving the efficiency of asymmetric induction. Also utilized in the development of ligands for transition-metal-catalyzed transformations.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 50mg | 10-20 days | ฿3,440.00 |
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| 100mg | 10-20 days | ฿4,700.00 |
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(4S)-4-(sec-Butyl)-2-(pyridin-2-yl)-4, 5-dihydrooxazole
Used as a chiral auxiliary in asymmetric synthesis, enabling the formation of enantiomerically enriched compounds. Its oxazoline core coordinates effectively with metal catalysts, making it valuable in catalytic asymmetric reactions such as aldol additions, alkylations, and Diels-Alder reactions. Commonly employed in pharmaceutical synthesis where stereochemical control is critical. The sec-butyl group enhances stereoselectivity due to its steric bulk, improving the efficiency of asymmetric induction. Also utilized in the development of ligands for transition-metal-catalyzed transformations.
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