tert-Butyl 4-[(1R)-1-aminoethyl]piperidine-1-carboxylate
≥95%
- Product Code: 83844
CAS:
1036027-86-7
| Molecular Weight: | 228.33 g./mol | Molecular Formula: | C₁₂H₂₄N₂O₂ |
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| EC Number: | MDL Number: | MFCD22666109 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, protected from light, stored under inert gas |
Product Description:
This compound is widely utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring a piperidine ring and a tert-butyl group, makes it particularly valuable in the development of drugs targeting the central nervous system (CNS). It is often employed in the production of compounds with potential therapeutic effects on neurological disorders, such as Alzheimer's disease, Parkinson's disease, and depression. Additionally, its chiral center allows for the creation of enantiomerically pure substances, which is crucial for enhancing the efficacy and reducing the side effects of medications. The compound's stability and reactivity also make it a preferred choice in medicinal chemistry research for designing and optimizing drug candidates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿4,725.00 |
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tert-Butyl 4-[(1R)-1-aminoethyl]piperidine-1-carboxylate
This compound is widely utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring a piperidine ring and a tert-butyl group, makes it particularly valuable in the development of drugs targeting the central nervous system (CNS). It is often employed in the production of compounds with potential therapeutic effects on neurological disorders, such as Alzheimer's disease, Parkinson's disease, and depression. Additionally, its chiral center allows for the creation of enantiomerically pure substances, which is crucial for enhancing the efficacy and reducing the side effects of medications. The compound's stability and reactivity also make it a preferred choice in medicinal chemistry research for designing and optimizing drug candidates.
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