Benzyl (2R,4R)-5-oxo-2,4-diphenyloxazolidine-3-carboxylate
98%
- Product Code: 229388
CAS:
205654-83-7
| Molecular Weight: | 373.4 g./mol | Molecular Formula: | C₂₃H₁₉NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD32644135 | |
| Melting Point: | Boiling Point: | 591.6±50.0 °C(Predicted) | |
| Density: | 1.270±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used as a chiral auxiliary in asymmetric synthesis, particularly in enantioselective alkylation and aldol reactions. Its rigid oxazolidine ring structure helps control stereochemistry, enabling high diastereoselectivity. Commonly employed in the pharmaceutical industry for the synthesis of optically active compounds, including active pharmaceutical ingredients (APIs) where stereo purity is critical. After serving its purpose, the auxiliary can be cleaved under mild conditions, leaving the desired chiral product intact. Also utilized in the development of chiral ligands and catalysts for transition-metal-mediated reactions.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿11,730.00 |
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| 0.250 | 10-20 days | ฿19,940.00 |
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Benzyl (2R,4R)-5-oxo-2,4-diphenyloxazolidine-3-carboxylate
Used as a chiral auxiliary in asymmetric synthesis, particularly in enantioselective alkylation and aldol reactions. Its rigid oxazolidine ring structure helps control stereochemistry, enabling high diastereoselectivity. Commonly employed in the pharmaceutical industry for the synthesis of optically active compounds, including active pharmaceutical ingredients (APIs) where stereo purity is critical. After serving its purpose, the auxiliary can be cleaved under mild conditions, leaving the desired chiral product intact. Also utilized in the development of chiral ligands and catalysts for transition-metal-mediated reactions.
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