tert-Butyl 4-(2-aminopropan-2-yl)piperidine-1-carboxylate
97%
- Product Code: 118528
CAS:
530116-33-7
| Molecular Weight: | 242.36 g./mol | Molecular Formula: | C₁₃H₂₆N₂O₂ |
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| EC Number: | MDL Number: | MFCD22034255 | |
| Melting Point: | Boiling Point: | ||
| 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 a key intermediate in the synthesis of various bioactive molecules. Its structure, featuring a piperidine ring and a tert-butyl group, makes it a valuable building block for creating compounds with potential therapeutic applications. It is often employed in the design and synthesis of drugs targeting neurological disorders, such as Alzheimer’s disease, due to its ability to modulate specific receptors in the brain. Additionally, it is used in the preparation of small molecule inhibitors and other pharmacologically active agents, contributing to advancements in medicinal chemistry. Its stability and reactivity also make it suitable for use in organic synthesis and combinatorial chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,141.00 |
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| 0.250 | 10-20 days | ฿5,337.00 |
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| 1.000 | 10-20 days | ฿14,391.00 |
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tert-Butyl 4-(2-aminopropan-2-yl)piperidine-1-carboxylate
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of various bioactive molecules. Its structure, featuring a piperidine ring and a tert-butyl group, makes it a valuable building block for creating compounds with potential therapeutic applications. It is often employed in the design and synthesis of drugs targeting neurological disorders, such as Alzheimer’s disease, due to its ability to modulate specific receptors in the brain. Additionally, it is used in the preparation of small molecule inhibitors and other pharmacologically active agents, contributing to advancements in medicinal chemistry. Its stability and reactivity also make it suitable for use in organic synthesis and combinatorial chemistry.
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