tert-Butyl 4-((2-methoxyethyl)amino)piperidine-1-carboxylate
97%
- Product Code: 118542
CAS:
710972-40-0
| Molecular Weight: | 258.36 g./mol | Molecular Formula: | C₁₃H₂₆N₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06656630 | |
| Melting Point: | Boiling Point: | 337.6°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, protected from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in pharmaceutical research and development as an intermediate in the synthesis of various biologically active molecules. Its structure, featuring both piperidine and tert-butyl groups, makes it a valuable building block for designing compounds targeting neurological and cardiovascular systems. It is often employed in the creation of potential drug candidates for conditions such as hypertension, anxiety, and depression. Additionally, its functional groups allow for further chemical modifications, enabling the exploration of diverse therapeutic agents. Researchers also use it in the study of enzyme inhibition and receptor binding mechanisms, contributing to the development of novel medications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $13.56 |
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| 0.250 | 10-20 days | $29.38 |
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| 1.000 | 10-20 days | $99.45 |
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| 5.000 | 10-20 days | $360.72 |
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tert-Butyl 4-((2-methoxyethyl)amino)piperidine-1-carboxylate
This compound is primarily utilized in pharmaceutical research and development as an intermediate in the synthesis of various biologically active molecules. Its structure, featuring both piperidine and tert-butyl groups, makes it a valuable building block for designing compounds targeting neurological and cardiovascular systems. It is often employed in the creation of potential drug candidates for conditions such as hypertension, anxiety, and depression. Additionally, its functional groups allow for further chemical modifications, enabling the exploration of diverse therapeutic agents. Researchers also use it in the study of enzyme inhibition and receptor binding mechanisms, contributing to the development of novel medications.
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