(R)-4-Phenyl-3-propionyl-2-oxazolidinone
≥98%,≥99% e.e.
- Product Code: 62486
CAS:
160695-26-1
| Molecular Weight: | 2219.2 g./mol | Molecular Formula: | C₁₂H₁₃NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 84°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is widely used as a chiral auxiliary in asymmetric synthesis, particularly in the formation of stereoselective carbon-carbon bonds. It is often employed in the synthesis of complex organic molecules, including pharmaceuticals, where controlling the stereochemistry is crucial. The chiral oxazolidinone framework helps induce high enantioselectivity in reactions such as aldol additions, alkylations, and Diels-Alder reactions. Additionally, it is utilized in the preparation of β-lactam antibiotics and other biologically active compounds, enhancing the efficiency and selectivity of synthetic routes. Its ability to provide predictable and consistent stereochemical outcomes makes it a valuable tool in medicinal chemistry and drug development.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | yellow solid |
| PURITY | 98-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿2,061.00 |
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| 5.000 | 10-20 days | ฿7,110.00 |
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(R)-4-Phenyl-3-propionyl-2-oxazolidinone
This compound is widely used as a chiral auxiliary in asymmetric synthesis, particularly in the formation of stereoselective carbon-carbon bonds. It is often employed in the synthesis of complex organic molecules, including pharmaceuticals, where controlling the stereochemistry is crucial. The chiral oxazolidinone framework helps induce high enantioselectivity in reactions such as aldol additions, alkylations, and Diels-Alder reactions. Additionally, it is utilized in the preparation of β-lactam antibiotics and other biologically active compounds, enhancing the efficiency and selectivity of synthetic routes. Its ability to provide predictable and consistent stereochemical outcomes makes it a valuable tool in medicinal chemistry and drug development.
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