(2R,4S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-hydroxypiperidine-2-carboxylic acid
95%
- Product Code: 228663
CAS:
917099-02-6
| Molecular Weight: | 367.4 g./mol | Molecular Formula: | C₂₁H₂₁NO₅ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 606.8±55.0 °C(Predicted) | |
| Density: | 1.367±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Widely used in peptide synthesis and medicinal chemistry, this compound serves as a key chiral building block for the development of protease inhibitors and other biologically active molecules. Its hydroxyl and carboxylic acid functional groups allow for selective modifications, enabling the construction of complex molecular architectures. The Fmoc-protected piperidine scaffold provides structural rigidity and stereochemical control, making it valuable in the synthesis of pharmaceutical intermediates, particularly in the design of enzyme inhibitors and receptor modulators. It is also employed in solid-phase peptide synthesis where preservation of stereochemistry is critical.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿11,540.00 |
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| 1g | 10-20 days | ฿52,950.00 |
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(2R,4S)-1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-4-hydroxypiperidine-2-carboxylic acid
Widely used in peptide synthesis and medicinal chemistry, this compound serves as a key chiral building block for the development of protease inhibitors and other biologically active molecules. Its hydroxyl and carboxylic acid functional groups allow for selective modifications, enabling the construction of complex molecular architectures. The Fmoc-protected piperidine scaffold provides structural rigidity and stereochemical control, making it valuable in the synthesis of pharmaceutical intermediates, particularly in the design of enzyme inhibitors and receptor modulators. It is also employed in solid-phase peptide synthesis where preservation of stereochemistry is critical.
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