Benzyl 3-(tert-butoxycarbonylamino)piperidine-1-carboxylate
95%
- Product Code: 124166
CAS:
406213-47-6
| Molecular Weight: | 334.41 g./mol | Molecular Formula: | C₁₈H₂₆N₂O₄ |
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| EC Number: | MDL Number: | MFCD09952600 | |
| Melting Point: | Boiling Point: | 471.9±44.0 °C(Predicte | |
| Density: | 1.15±0.1 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in pharmaceutical research and development as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It plays a significant role in the preparation of compounds targeting neurological disorders, such as Alzheimer's disease and other cognitive impairments, due to its piperidine moiety, which is a common structural feature in many CNS-active drugs. Additionally, it is utilized in the production of peptidomimetics and protease inhibitors, which are essential in treating viral infections like HIV and hepatitis. Its tert-butoxycarbonyl (Boc) protecting group ensures stability during synthetic processes, making it valuable in multi-step organic synthesis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $109.14 |
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| 0.250 | 10-20 days | $210.05 |
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| 1.000 | 10-20 days | $420.48 |
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Benzyl 3-(tert-butoxycarbonylamino)piperidine-1-carboxylate
This chemical is primarily used in pharmaceutical research and development as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). It plays a significant role in the preparation of compounds targeting neurological disorders, such as Alzheimer's disease and other cognitive impairments, due to its piperidine moiety, which is a common structural feature in many CNS-active drugs. Additionally, it is utilized in the production of peptidomimetics and protease inhibitors, which are essential in treating viral infections like HIV and hepatitis. Its tert-butoxycarbonyl (Boc) protecting group ensures stability during synthetic processes, making it valuable in multi-step organic synthesis.
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