(2R,3S,4R,5R)-5-(((Allyloxy)carbonyl)amino)-2-hydroxy-6-oxohexane-1,3,4-triyl triacetate
95%
- Product Code: 228754
CAS:
1374760-23-2
| Molecular Weight: | 389.35 g./mol | Molecular Formula: | C₁₆H₂₃NO₁₀ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 542.3±50.0 °C(Predicted) | |
| Density: | 1.269±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C |
Product Description:
Used as an intermediate in the synthesis of antiviral and antibiotic agents, particularly in the preparation of nucleoside analogs. Its protected hydroxyl and amino groups allow selective reactions in multi-step organic syntheses. Commonly employed in pharmaceutical research for prodrug development, where the allyl carbamate group acts as a cleavable protecting group under mild conditions. Also utilized in the production of glycosyl donors for oligosaccharide assembly due to its stereochemistry and functional group compatibility.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿2,400.00 |
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| 500mg | 10-20 days | ฿6,000.00 |
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| 1g | 10-20 days | ฿9,600.00 |
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(2R,3S,4R,5R)-5-(((Allyloxy)carbonyl)amino)-2-hydroxy-6-oxohexane-1,3,4-triyl triacetate
Used as an intermediate in the synthesis of antiviral and antibiotic agents, particularly in the preparation of nucleoside analogs. Its protected hydroxyl and amino groups allow selective reactions in multi-step organic syntheses. Commonly employed in pharmaceutical research for prodrug development, where the allyl carbamate group acts as a cleavable protecting group under mild conditions. Also utilized in the production of glycosyl donors for oligosaccharide assembly due to its stereochemistry and functional group compatibility.
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