(2R,3R)-2,3-Bis(acetyloxy)butanedioic Acid
≥98%
- Product Code: 71205
CAS:
51591-38-9
| Molecular Weight: | 234.2 g./mol | Molecular Formula: | C₈H₁₀O₈ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | 118 °C | Boiling Point: | 398.9±42.0 °C |
| Density: | 1.486±0.06 g/mL | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the synthesis of chiral intermediates for pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) that require specific stereochemistry. Its diacetylated structure makes it a valuable precursor in organic synthesis, enabling the creation of complex molecules with high enantiomeric purity. Additionally, it finds application in the development of fine chemicals and specialty compounds used in research and industrial processes. Its role in asymmetric synthesis is significant, often aiding in the construction of biologically active molecules with precise three-dimensional configurations.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Almost white powder to crystal |
| PURITY | 98-100 |
| Infrared spectrum | Conforms to Structure |
| MELTING POINT C | 119.0-122.0 |
| Specific rotation a20DC10 Aceton | -24.0 -26.0 |
| SOLUBILITY IN ACETONE | almost transparency |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $56.25 |
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| 5.000 | 10-20 days | $229.03 |
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(2R,3R)-2,3-Bis(acetyloxy)butanedioic Acid
This compound is primarily utilized in the synthesis of chiral intermediates for pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) that require specific stereochemistry. Its diacetylated structure makes it a valuable precursor in organic synthesis, enabling the creation of complex molecules with high enantiomeric purity. Additionally, it finds application in the development of fine chemicals and specialty compounds used in research and industrial processes. Its role in asymmetric synthesis is significant, often aiding in the construction of biologically active molecules with precise three-dimensional configurations.
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