Benzyl (3S,4R)-3-((tert-butoxycarbonyl)amino)-4-hydroxypiperidine-1-carboxylate
95%
- Product Code: 82889
CAS:
1549812-60-3
| Molecular Weight: | 350.42 g./mol | Molecular Formula: | C₁₈H₂₆N₂O₅ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD31656832 | |
| Melting Point: | Boiling Point: | 512.9±50.0 °C(Predicted) | |
| Density: | 1.22±0.1 g/cm3(Predicted) | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in the synthesis of complex pharmaceutical agents, particularly in the development of protease inhibitors and other therapeutic molecules targeting various diseases. Its structure, featuring both a Boc-protected amino group and a hydroxyl group, makes it a valuable intermediate in organic synthesis, enabling the construction of intricate molecular frameworks. It is often employed in peptide chemistry and medicinal chemistry research, where precise control over stereochemistry and functional group manipulation is crucial. Additionally, it serves as a building block in the preparation of biologically active compounds, contributing to advancements in drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $951.02 |
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| 0.250 | 10-20 days | $1,902.04 |
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Benzyl (3S,4R)-3-((tert-butoxycarbonyl)amino)-4-hydroxypiperidine-1-carboxylate
This compound is primarily utilized in the synthesis of complex pharmaceutical agents, particularly in the development of protease inhibitors and other therapeutic molecules targeting various diseases. Its structure, featuring both a Boc-protected amino group and a hydroxyl group, makes it a valuable intermediate in organic synthesis, enabling the construction of intricate molecular frameworks. It is often employed in peptide chemistry and medicinal chemistry research, where precise control over stereochemistry and functional group manipulation is crucial. Additionally, it serves as a building block in the preparation of biologically active compounds, contributing to advancements in drug discovery and development.
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