(S)-N-Boc-2,2-dimethyloxazolidine-4-carboxylic Acid
98%
- Product Code: 57174
CAS:
139009-66-8
| Molecular Weight: | 245.27 g./mol | Molecular Formula: | C₁₁H₁₉NO₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02682656 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the synthesis of chiral molecules, particularly in the field of organic chemistry and pharmaceutical research. Its structure makes it a valuable intermediate for the preparation of enantiomerically pure compounds, which are crucial in the development of active pharmaceutical ingredients (APIs). The Boc (tert-butoxycarbonyl) protecting group ensures stability during synthetic processes, while the oxazolidine ring provides a rigid framework that aids in stereocontrol. It is often employed in the synthesis of beta-amino acids, peptidomimetics, and other biologically active molecules. Additionally, its chiral nature allows for the creation of compounds with specific three-dimensional configurations, which is essential for optimizing drug efficacy and reducing side effects.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | £41.84 |
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| 1.000 | 10-20 days | £114.22 |
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(S)-N-Boc-2,2-dimethyloxazolidine-4-carboxylic Acid
This compound is primarily utilized in the synthesis of chiral molecules, particularly in the field of organic chemistry and pharmaceutical research. Its structure makes it a valuable intermediate for the preparation of enantiomerically pure compounds, which are crucial in the development of active pharmaceutical ingredients (APIs). The Boc (tert-butoxycarbonyl) protecting group ensures stability during synthetic processes, while the oxazolidine ring provides a rigid framework that aids in stereocontrol. It is often employed in the synthesis of beta-amino acids, peptidomimetics, and other biologically active molecules. Additionally, its chiral nature allows for the creation of compounds with specific three-dimensional configurations, which is essential for optimizing drug efficacy and reducing side effects.
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