(S)-tert-Butyl cyclopropyl(piperidin-3-yl)carbamate
≥95%
- Product Code: 113859
CAS:
250275-25-3
| Molecular Weight: | 240.34 g./mol | Molecular Formula: | C₁₃H₂₄N₂O₂ |
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| EC Number: | MDL Number: | MFCD21098144 | |
| 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 the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a piperidine ring and a cyclopropyl group, makes it a valuable building block for developing pharmaceutical agents, particularly those targeting the central nervous system. It is often employed in the preparation of potential drug candidates for neurological disorders, such as Alzheimer's disease or Parkinson's disease, due to its ability to modulate specific receptors or enzymes in the brain. Additionally, its tert-butyl carbamate group provides stability and protection during synthetic processes, enabling efficient multi-step reactions. Researchers also explore its use in creating novel compounds with potential anti-inflammatory or analgesic properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | Ft149,426.10 |
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| 0.250 | 10-20 days | Ft298,755.24 |
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(S)-tert-Butyl cyclopropyl(piperidin-3-yl)carbamate
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a piperidine ring and a cyclopropyl group, makes it a valuable building block for developing pharmaceutical agents, particularly those targeting the central nervous system. It is often employed in the preparation of potential drug candidates for neurological disorders, such as Alzheimer's disease or Parkinson's disease, due to its ability to modulate specific receptors or enzymes in the brain. Additionally, its tert-butyl carbamate group provides stability and protection during synthetic processes, enabling efficient multi-step reactions. Researchers also explore its use in creating novel compounds with potential anti-inflammatory or analgesic properties.
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