(S)-3-(tert-Butoxycarbonyl)oxazolidine-4-carboxylic acid
97%
- Product Code: 232539
CAS:
161979-35-7
| Molecular Weight: | 217.22 g./mol | Molecular Formula: | C₉H₁₅NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28403376 | |
| Melting Point: | Boiling Point: | 355.1±42.0 °C(Predicted) | |
| Density: | 1.275±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry, light-proof |
Product Description:
Used as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of enantiomerically pure compounds such as pharmaceuticals and fine chemicals. Its rigid oxazolidine ring structure facilitates high stereoselectivity in reactions like aldol condensations, alkylations, and Diels-Alder reactions. Commonly employed in the synthesis of β-amino acids and other bioactive molecules where control of stereochemistry is critical. The tert-butoxycarbonyl (Boc) group allows for easy protection and deprotection of the nitrogen, making it compatible with multi-step synthetic sequences. Widely utilized in medicinal chemistry and process development for drug manufacturing.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿9,830.00 |
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| 250mg | 10-20 days | ฿16,710.00 |
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| 1g | 10-20 days | ฿45,100.00 |
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(S)-3-(tert-Butoxycarbonyl)oxazolidine-4-carboxylic acid
Used as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of enantiomerically pure compounds such as pharmaceuticals and fine chemicals. Its rigid oxazolidine ring structure facilitates high stereoselectivity in reactions like aldol condensations, alkylations, and Diels-Alder reactions. Commonly employed in the synthesis of β-amino acids and other bioactive molecules where control of stereochemistry is critical. The tert-butoxycarbonyl (Boc) group allows for easy protection and deprotection of the nitrogen, making it compatible with multi-step synthetic sequences. Widely utilized in medicinal chemistry and process development for drug manufacturing.
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