Methyl 2-oxo-2-(1-1-[(pyridin-2-yl)methyl]piperidin-4-yl-1H-indol-3-yl)acetate
90%
- Product Code: 42497
CAS:
616898-64-7
| Molecular Weight: | 377.4363 g./mol | Molecular Formula: | C₂₂H₂₃N₃O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09833915 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring indole and piperidine moieties, makes it a valuable intermediate in the design of molecules targeting neurological disorders, such as Alzheimer's disease and other cognitive impairments. The pyridine ring enhances its potential as a ligand for receptors in the central nervous system, aiding in the development of compounds with improved binding affinity and selectivity. Additionally, it may be explored for its role in modulating enzyme activity or as a precursor in the creation of bioactive molecules with potential therapeutic applications. Its ester group also allows for further chemical modifications, enabling the synthesis of diverse derivatives for drug discovery programs.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $357.32 |
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Methyl 2-oxo-2-(1-1-[(pyridin-2-yl)methyl]piperidin-4-yl-1H-indol-3-yl)acetate
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring indole and piperidine moieties, makes it a valuable intermediate in the design of molecules targeting neurological disorders, such as Alzheimer's disease and other cognitive impairments. The pyridine ring enhances its potential as a ligand for receptors in the central nervous system, aiding in the development of compounds with improved binding affinity and selectivity. Additionally, it may be explored for its role in modulating enzyme activity or as a precursor in the creation of bioactive molecules with potential therapeutic applications. Its ester group also allows for further chemical modifications, enabling the synthesis of diverse derivatives for drug discovery programs.
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