(3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl 4-nitrophenyl carbonate
95%
- Product Code: 36744
CAS:
192725-55-6
| Molecular Weight: | 295.24 g./mol | Molecular Formula: | C₁₃H₁₃NO₇ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22200696 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, airtight |
Product Description:
This compound is primarily utilized in organic synthesis as a protecting group for hydroxyl functionalities, particularly in the preparation of complex molecules such as peptides and carbohydrates. Its stability under various reaction conditions makes it a valuable tool in multi-step synthetic processes. Additionally, it is employed in the development of prodrugs, where it acts as a cleavable linker to release active pharmaceutical ingredients in a controlled manner. The compound's ability to undergo selective deprotection under mild conditions further enhances its utility in targeted drug delivery systems. It is also explored in the field of bioconjugation, where it facilitates the attachment of bioactive molecules to carriers or surfaces for diagnostic or therapeutic purposes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿10,800.00 |
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| 0.250 | 10-20 days | ฿20,250.00 |
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| 1.000 | 10-20 days | ฿40,500.00 |
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(3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl 4-nitrophenyl carbonate
This compound is primarily utilized in organic synthesis as a protecting group for hydroxyl functionalities, particularly in the preparation of complex molecules such as peptides and carbohydrates. Its stability under various reaction conditions makes it a valuable tool in multi-step synthetic processes. Additionally, it is employed in the development of prodrugs, where it acts as a cleavable linker to release active pharmaceutical ingredients in a controlled manner. The compound's ability to undergo selective deprotection under mild conditions further enhances its utility in targeted drug delivery systems. It is also explored in the field of bioconjugation, where it facilitates the attachment of bioactive molecules to carriers or surfaces for diagnostic or therapeutic purposes.
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