(2S,3R)-Methyl 2-amino-3-hydroxybutanoate
98%
- Product Code: 104145
CAS:
3373-59-9
| Molecular Weight: | 133.15 g./mol | Molecular Formula: | C₅H₁₁NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00075749 | |
| Melting Point: | Boiling Point: | 238.58 °C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, protected from light, inert gas |
Product Description:
This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the production of antibiotics and other therapeutic agents. Its chiral structure makes it valuable for creating enantiomerically pure drugs, which are crucial for ensuring efficacy and reducing side effects. Additionally, it serves as a building block in organic synthesis, enabling the development of complex molecules with specific biological activities. In research, it is often employed as a precursor for studying enzyme mechanisms and developing new catalytic processes. Its applications extend to the field of biochemistry, where it is used in peptide synthesis and the modification of biomolecules to enhance their properties.
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 |
|---|---|---|---|
| 1.000 | 10-20 days | ฿2,260.00 |
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| 5.000 | 10-20 days | ฿8,680.00 |
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(2S,3R)-Methyl 2-amino-3-hydroxybutanoate
This compound is primarily utilized in the synthesis of pharmaceuticals, particularly in the production of antibiotics and other therapeutic agents. Its chiral structure makes it valuable for creating enantiomerically pure drugs, which are crucial for ensuring efficacy and reducing side effects. Additionally, it serves as a building block in organic synthesis, enabling the development of complex molecules with specific biological activities. In research, it is often employed as a precursor for studying enzyme mechanisms and developing new catalytic processes. Its applications extend to the field of biochemistry, where it is used in peptide synthesis and the modification of biomolecules to enhance their properties.
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