2,5-Dioxopyrrolidin-1-yl ((3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl) carbonate
≥95%
- Product Code: 40894
CAS:
253265-97-3
| Molecular Weight: | 271.22 g./mol | Molecular Formula: | C₁₁H₁₃NO₇ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12031467 | |
| Melting Point: | Boiling Point: | 391.8°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily utilized as a key intermediate in the synthesis of complex pharmaceutical compounds, particularly in the development of antiviral medications. Its structure is crucial for the formation of prodrugs, which enhance the bioavailability and stability of active pharmaceutical ingredients. It is often employed in the production of HIV protease inhibitors, where it facilitates the delivery of the active drug to target sites more effectively. Additionally, its unique stereochemistry makes it valuable in asymmetric synthesis, enabling the creation of enantiomerically pure compounds for therapeutic use. Its application extends to research settings, where it serves as a building block for the development of novel drug candidates and the study of biochemical pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $68.32 |
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| 0.250 | 10-20 days | $102.34 |
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| 1.000 | 10-20 days | $409.09 |
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| 5.000 | 10-20 days | $2,037.35 |
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2,5-Dioxopyrrolidin-1-yl ((3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl) carbonate
This chemical is primarily utilized as a key intermediate in the synthesis of complex pharmaceutical compounds, particularly in the development of antiviral medications. Its structure is crucial for the formation of prodrugs, which enhance the bioavailability and stability of active pharmaceutical ingredients. It is often employed in the production of HIV protease inhibitors, where it facilitates the delivery of the active drug to target sites more effectively. Additionally, its unique stereochemistry makes it valuable in asymmetric synthesis, enabling the creation of enantiomerically pure compounds for therapeutic use. Its application extends to research settings, where it serves as a building block for the development of novel drug candidates and the study of biochemical pathways.
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