tert-Butyl 4-benzyl-4-cyanopiperidine-1-carboxylate
97%
- Product Code: 124339
CAS:
906329-30-4
| Molecular Weight: | 300.4 g./mol | Molecular Formula: | C₁₈H₂₄N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11849801 | |
| Melting Point: | Boiling Point: | 216.9±40.0 °C(Predicted) | |
| Density: | 0.947±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This compound is primarily utilized in organic synthesis as an intermediate for the development of pharmaceuticals and bioactive molecules. Its structure, featuring a piperidine ring, benzyl group, and cyano substituent, makes it a valuable building block in medicinal chemistry. It is often employed in the synthesis of compounds targeting neurological disorders, such as inhibitors for enzymes or receptors involved in the central nervous system. Additionally, it serves as a precursor in the preparation of complex molecules for drug discovery, particularly in the optimization of pharmacokinetic properties and biological activity. Its stability and reactivity allow for versatile modifications, making it a key component in the design of novel therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿7,650.00 |
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| 0.250 | 10-20 days | ฿13,005.00 |
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| 1.000 | 10-20 days | ฿35,100.00 |
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tert-Butyl 4-benzyl-4-cyanopiperidine-1-carboxylate
This compound is primarily utilized in organic synthesis as an intermediate for the development of pharmaceuticals and bioactive molecules. Its structure, featuring a piperidine ring, benzyl group, and cyano substituent, makes it a valuable building block in medicinal chemistry. It is often employed in the synthesis of compounds targeting neurological disorders, such as inhibitors for enzymes or receptors involved in the central nervous system. Additionally, it serves as a precursor in the preparation of complex molecules for drug discovery, particularly in the optimization of pharmacokinetic properties and biological activity. Its stability and reactivity allow for versatile modifications, making it a key component in the design of novel therapeutic agents.
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