tert-Butyl 3-((3-methoxypropyl)amino)piperidine-1-carboxylate
95%
- Product Code: 39701
CAS:
887588-18-3
| Molecular Weight: | 272.3800 g./mol | Molecular Formula: | C₁₄H₂₈N₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06656638 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as an intermediate for the development of more complex molecules, particularly in pharmaceutical research. It serves as a key building block in the synthesis of compounds with potential biological activity, such as inhibitors or modulators of specific enzymes or receptors. Its structure, featuring both piperidine and methoxypropylamino groups, makes it suitable for creating molecules that interact with central nervous system targets. Additionally, it is often employed in medicinal chemistry to optimize drug candidates for improved pharmacokinetic properties, such as solubility and bioavailability. Its tert-butyloxycarbonyl (Boc) protecting group allows for selective reactions during multi-step synthetic processes.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 G | 10-20 days | ฿3,960.00 |
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tert-Butyl 3-((3-methoxypropyl)amino)piperidine-1-carboxylate
This compound is primarily utilized in organic synthesis as an intermediate for the development of more complex molecules, particularly in pharmaceutical research. It serves as a key building block in the synthesis of compounds with potential biological activity, such as inhibitors or modulators of specific enzymes or receptors. Its structure, featuring both piperidine and methoxypropylamino groups, makes it suitable for creating molecules that interact with central nervous system targets. Additionally, it is often employed in medicinal chemistry to optimize drug candidates for improved pharmacokinetic properties, such as solubility and bioavailability. Its tert-butyloxycarbonyl (Boc) protecting group allows for selective reactions during multi-step synthetic processes.
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