(S)-tert-butyl 2-formylpiperidine-1-carboxylate
≥95%
- Product Code: 234682
CAS:
150521-32-7
| Molecular Weight: | 213.27 g./mol | Molecular Formula: | C₁₁H₁₉NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06738713 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature |
Product Description:
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its aldehyde functionality allows for further derivatization through reactions such as reductive amination or nucleophilic addition, enabling the construction of complex nitrogen-containing heterocycles. Commonly employed in medicinal chemistry for the preparation of protease inhibitors, receptor agonists, and other bioactive molecules where the (S)-configuration is critical for biological activity. The tert-butyl carbamate (Boc) group provides stability and acts as a protecting group during multi-step syntheses, allowing selective deprotection under mild acidic conditions.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿1,220.00 |
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| 1g | 10-20 days | ฿3,200.00 |
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| 5g | 10-20 days | ฿12,800.00 |
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| 10g | 10-20 days | ฿19,200.00 |
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| 25g | 10-20 days | ฿40,000.00 |
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(S)-tert-butyl 2-formylpiperidine-1-carboxylate
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring stereochemical control. Its aldehyde functionality allows for further derivatization through reactions such as reductive amination or nucleophilic addition, enabling the construction of complex nitrogen-containing heterocycles. Commonly employed in medicinal chemistry for the preparation of protease inhibitors, receptor agonists, and other bioactive molecules where the (S)-configuration is critical for biological activity. The tert-butyl carbamate (Boc) group provides stability and acts as a protecting group during multi-step syntheses, allowing selective deprotection under mild acidic conditions.
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| Stable in pH range | - |
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