tert-Butyl 3,3-difluoro-4-formylpiperidine-1-carboxylate
97%
- Product Code: 131306
CAS:
1373503-65-1
| Molecular Weight: | 249.25 g./mol | Molecular Formula: | C₁₁H₁₇F₂NO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22199367 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | -20°C, Sealed, Inert Gas |
Product Description:
Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of fluorinated drug candidates. The aldehyde group allows for further functionalization through reactions such as reductive amination or Wittig reactions, enabling the construction of complex molecular architectures. The tert-butyl carbamate (Boc) group provides amine protection during multi-step syntheses, ensuring selective reactivity. Its piperidine core with geminal difluoro substitution enhances metabolic stability and membrane permeability in bioactive molecules, making it valuable in medicinal chemistry for CNS-targeted drugs and enzyme inhibitors.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿19,290.00 |
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| 0.250 | 10-20 days | ฿31,260.00 |
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tert-Butyl 3,3-difluoro-4-formylpiperidine-1-carboxylate
Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of fluorinated drug candidates. The aldehyde group allows for further functionalization through reactions such as reductive amination or Wittig reactions, enabling the construction of complex molecular architectures. The tert-butyl carbamate (Boc) group provides amine protection during multi-step syntheses, ensuring selective reactivity. Its piperidine core with geminal difluoro substitution enhances metabolic stability and membrane permeability in bioactive molecules, making it valuable in medicinal chemistry for CNS-targeted drugs and enzyme inhibitors.
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