(4S,5R)-tert-Butyl 4-formyl-2,2,5-trimethyloxazolidine-3-carboxylate
97%
- Product Code: 232505
CAS:
108149-62-8
| Molecular Weight: | 243.3054 g./mol | Molecular Formula: | C₁₂H₂₁NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD16613945 | |
| Melting Point: | Boiling Point: | 312.4±42.0 °C(Predicted) | |
| Density: | 1.091±0.06 g/cm3(Predicted) | Storage Condition: | -20°C, Inert Gas |
Product Description:
Used as a chiral auxiliary in asymmetric synthesis, this compound enables the stereocontrolled formation of complex organic molecules. Its rigid oxazolidine ring and defined stereocenters make it valuable for directing selective reactions, particularly in pharmaceutical intermediates where precise 3D arrangement is critical. The aldehyde and ester functionalities allow for further chemical transformations, such as chain elongation or cyclization, while the tert-butyl group enhances stability and solubility in organic solvents. Commonly employed in multi-step synthesis of bioactive compounds, it supports high enantioselectivity in aldol, alkylation, and Diels-Alder reactions.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿8,170.00 |
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| 0.100 | 10-20 days | ฿13,890.00 |
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(4S,5R)-tert-Butyl 4-formyl-2,2,5-trimethyloxazolidine-3-carboxylate
Used as a chiral auxiliary in asymmetric synthesis, this compound enables the stereocontrolled formation of complex organic molecules. Its rigid oxazolidine ring and defined stereocenters make it valuable for directing selective reactions, particularly in pharmaceutical intermediates where precise 3D arrangement is critical. The aldehyde and ester functionalities allow for further chemical transformations, such as chain elongation or cyclization, while the tert-butyl group enhances stability and solubility in organic solvents. Commonly employed in multi-step synthesis of bioactive compounds, it supports high enantioselectivity in aldol, alkylation, and Diels-Alder reactions.
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