1-Boc-piperidine-3-carboxaldehyde
97%
- Product Code: 143498
CAS:
118156-93-7
| Molecular Weight: | 213.28 g./mol | Molecular Formula: | C₁₁H₁₉NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD02179020 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature |
Product Description:
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that require functionalized piperidine scaffolds. Its aldehyde group allows for further chemical transformations such as reductive amination or nucleophilic addition, enabling the construction of complex nitrogen-containing molecules. Commonly employed in medicinal chemistry for drug discovery programs, especially in the design of central nervous system (CNS) agents, kinase inhibitors, and bioactive molecules where a substituted piperidine ring enhances pharmacokinetic properties. The Boc-protected amine ensures selective reactivity and stability during multi-step syntheses, making it valuable in solid-phase and solution-phase peptide-like compound assembly.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 G | 10-20 days | ฿180.00 |
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| 1.000 G | 10-20 days | ฿310.00 |
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| 25.000 G | 10-20 days | ฿4,680.00 |
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| 100.000 G | 10-20 days | ฿16,020.00 |
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| 5.000 G | 10-20 days | ฿1,170.00 |
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1-Boc-piperidine-3-carboxaldehyde
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) that require functionalized piperidine scaffolds. Its aldehyde group allows for further chemical transformations such as reductive amination or nucleophilic addition, enabling the construction of complex nitrogen-containing molecules. Commonly employed in medicinal chemistry for drug discovery programs, especially in the design of central nervous system (CNS) agents, kinase inhibitors, and bioactive molecules where a substituted piperidine ring enhances pharmacokinetic properties. The Boc-protected amine ensures selective reactivity and stability during multi-step syntheses, making it valuable in solid-phase and solution-phase peptide-like compound assembly.
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| Stable in pH range | - |
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