tert-Butyl octahydro-1H-pyrrolo[3,2-b]pyridine-1-carboxylate
96%
- Product Code: 54868
CAS:
1211586-14-9
| Molecular Weight: | 226.3200 g./mol | Molecular Formula: | C₁₂H₂₂N₂O₂ |
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| EC Number: | MDL Number: | MFCD18382710 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of complex molecules. Its structure is particularly valuable in the creation of biologically active compounds, including potential drug candidates targeting neurological disorders and other therapeutic areas. The tert-butyl group provides steric protection, enhancing stability during chemical reactions, while the octahydro-pyrrolo-pyridine scaffold contributes to the molecule's ability to interact with biological targets. It is often employed in medicinal chemistry to optimize drug-like properties, such as solubility, bioavailability, and binding affinity. Additionally, its versatility makes it a useful building block in the preparation of libraries for high-throughput screening in drug discovery programs.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿7,245.00 |
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tert-Butyl octahydro-1H-pyrrolo[3,2-b]pyridine-1-carboxylate
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of complex molecules. Its structure is particularly valuable in the creation of biologically active compounds, including potential drug candidates targeting neurological disorders and other therapeutic areas. The tert-butyl group provides steric protection, enhancing stability during chemical reactions, while the octahydro-pyrrolo-pyridine scaffold contributes to the molecule's ability to interact with biological targets. It is often employed in medicinal chemistry to optimize drug-like properties, such as solubility, bioavailability, and binding affinity. Additionally, its versatility makes it a useful building block in the preparation of libraries for high-throughput screening in drug discovery programs.
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