tert-Butyl 4-allyl-4-(hydroxymethyl)piperidine-1-carboxylate
95%
- Product Code: 83837
CAS:
236406-37-4
| Molecular Weight: | 255.35 g./mol | Molecular Formula: | C₁₄H₂₅NO₃ |
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| EC Number: | MDL Number: | MFCD17676692 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex compounds. Its structure, featuring both a piperidine ring and an allyl group, makes it valuable for constructing pharmacologically active molecules, particularly in the development of pharmaceuticals targeting neurological disorders. The hydroxylmethyl group allows for further functionalization, enabling the creation of diverse derivatives with potential biological activity. Additionally, its tert-butyl carboxylate group provides stability and facilitates selective reactions in multi-step synthetic processes. It is also explored in the synthesis of ligands for receptor studies, aiding in drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $380.41 |
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| 0.250 | 10-20 days | $634.01 |
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| 1.000 | 10-20 days | $1,268.03 |
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tert-Butyl 4-allyl-4-(hydroxymethyl)piperidine-1-carboxylate
This chemical is primarily utilized in organic synthesis as a versatile intermediate for the preparation of more complex compounds. Its structure, featuring both a piperidine ring and an allyl group, makes it valuable for constructing pharmacologically active molecules, particularly in the development of pharmaceuticals targeting neurological disorders. The hydroxylmethyl group allows for further functionalization, enabling the creation of diverse derivatives with potential biological activity. Additionally, its tert-butyl carboxylate group provides stability and facilitates selective reactions in multi-step synthetic processes. It is also explored in the synthesis of ligands for receptor studies, aiding in drug discovery and development.
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