(2S,4S)-1-(tert-butoxycarbonyl)-2-methylpiperidine-4-carboxylicacid
98%
- Product Code: 237658
CAS:
1820583-83-2
| Molecular Weight: | 243.30 g./mol | Molecular Formula: | C₁₂H₂₁NO₄ |
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| EC Number: | MDL Number: | MFCD28139503 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, seal, dry |
Product Description:
Used as a key chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its stereochemistry allows for selective interactions in drug design, enhancing potency and specificity. Commonly employed in medicinal chemistry for constructing complex cyclic frameworks found in antiviral and anticancer agents. The Boc-protected amine and carboxylic acid functionalities enable stepwise coupling reactions, making it valuable in solid-phase and solution-phase peptide-like synthesis.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | $690.61 |
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| 500mg | 10-20 days | $1,937.13 |
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| 1g | 10-20 days | $3,390.28 |
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| 250mg | 10-20 days | $1,104.66 |
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(2S,4S)-1-(tert-butoxycarbonyl)-2-methylpiperidine-4-carboxylicacid
Used as a key chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its stereochemistry allows for selective interactions in drug design, enhancing potency and specificity. Commonly employed in medicinal chemistry for constructing complex cyclic frameworks found in antiviral and anticancer agents. The Boc-protected amine and carboxylic acid functionalities enable stepwise coupling reactions, making it valuable in solid-phase and solution-phase peptide-like synthesis.
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