cis-tert-Butyl 4-amino-3-methylpiperidine-1-carboxylate
97%
- Product Code: 123406
CAS:
1039741-10-0
| Molecular Weight: | 214.3 g./mol | Molecular Formula: | C₁₁H₂₂N₂O₂ |
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| EC Number: | MDL Number: | MFCD06803068 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dark, inert gas |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various biologically active molecules. Its structural features, including the piperidine ring and amino group, make it a valuable building block for developing drugs targeting the central nervous system. It is often employed in the preparation of compounds with potential applications in treating neurological disorders, such as Alzheimer's disease, Parkinson's disease, and other conditions involving neurotransmitter regulation. Additionally, its tert-butyl carboxylate group enhances stability and facilitates further chemical modifications, making it a versatile reagent in medicinal chemistry research and drug development processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $351.10 |
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| 0.250 | 10-20 days | $736.89 |
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cis-tert-Butyl 4-amino-3-methylpiperidine-1-carboxylate
This compound is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various biologically active molecules. Its structural features, including the piperidine ring and amino group, make it a valuable building block for developing drugs targeting the central nervous system. It is often employed in the preparation of compounds with potential applications in treating neurological disorders, such as Alzheimer's disease, Parkinson's disease, and other conditions involving neurotransmitter regulation. Additionally, its tert-butyl carboxylate group enhances stability and facilitates further chemical modifications, making it a versatile reagent in medicinal chemistry research and drug development processes.
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