(R)-tert-Butyl 3-(pyridin-2-yloxy)pyrrolidine-1-carboxylate
95%
- Product Code: 37583
CAS:
1417789-79-7
| Molecular Weight: | 264.3202 g./mol | Molecular Formula: | C₁₄H₂₀N₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD21606421 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of pharmaceutical research and development, particularly as an intermediate in the synthesis of bioactive molecules. Its structure, featuring a pyrrolidine ring and a pyridine moiety, 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 cognitive enhancers or treatments for neurodegenerative diseases. Additionally, its chiral nature allows for the development of enantiomerically pure compounds, which is crucial in optimizing drug efficacy and reducing side effects. The tert-butyl ester group in the molecule also provides stability and facilitates further chemical modifications during synthetic processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,435.00 |
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(R)-tert-Butyl 3-(pyridin-2-yloxy)pyrrolidine-1-carboxylate
This compound is primarily utilized in the field of pharmaceutical research and development, particularly as an intermediate in the synthesis of bioactive molecules. Its structure, featuring a pyrrolidine ring and a pyridine moiety, 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 cognitive enhancers or treatments for neurodegenerative diseases. Additionally, its chiral nature allows for the development of enantiomerically pure compounds, which is crucial in optimizing drug efficacy and reducing side effects. The tert-butyl ester group in the molecule also provides stability and facilitates further chemical modifications during synthetic processes.
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