(R)-Methyl 2,3-dihydroxypropanoate
95%
- Product Code: 37409
CAS:
18289-89-9
| Molecular Weight: | 120.10392 g./mol | Molecular Formula: | C₄H₈O₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06204263 | |
| Melting Point: | Boiling Point: | 140 ℃(Press: 15 Torr) | |
| Density: | 1.2795 g/cm3 | Storage Condition: | 2-8℃ |
Product Description:
(R)-Methyl 2,3-dihydroxypropanoate is primarily utilized in the synthesis of various pharmaceutical compounds, particularly those requiring chiral intermediates. Its dihydroxy structure makes it a valuable building block in the production of drugs targeting cardiovascular diseases, as it can be transformed into derivatives that act as beta-blockers or other heart-related medications. Additionally, it serves as a precursor in the synthesis of fine chemicals and agrochemicals, where its chiral nature is essential for achieving specific biological activities. In the field of organic chemistry, it is often employed in asymmetric synthesis to create enantiomerically pure compounds, which are crucial for developing high-efficacy drugs and advanced materials. Its application also extends to the production of specialty polymers and coatings, where its hydroxyl groups can be modified to enhance material properties.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless to Pale-yellow to Yellow-brown Liquid |
| PURITY | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿3,260.00 |
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| 5.000 | 10-20 days | ฿10,500.00 |
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(R)-Methyl 2,3-dihydroxypropanoate
(R)-Methyl 2,3-dihydroxypropanoate is primarily utilized in the synthesis of various pharmaceutical compounds, particularly those requiring chiral intermediates. Its dihydroxy structure makes it a valuable building block in the production of drugs targeting cardiovascular diseases, as it can be transformed into derivatives that act as beta-blockers or other heart-related medications. Additionally, it serves as a precursor in the synthesis of fine chemicals and agrochemicals, where its chiral nature is essential for achieving specific biological activities. In the field of organic chemistry, it is often employed in asymmetric synthesis to create enantiomerically pure compounds, which are crucial for developing high-efficacy drugs and advanced materials. Its application also extends to the production of specialty polymers and coatings, where its hydroxyl groups can be modified to enhance material properties.
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