tert-Butyl 8'-fluoro-2',4'-dihydro-1'H-spiro[piperidine-4,3'-quinoline]-1-carbox
95%
- Product Code: 75943
CAS:
1439900-44-3
| Molecular Weight: | 320.4 g./mol | Molecular Formula: | C₁₈H₂₅FN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD26096864 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of biologically active molecules, particularly those targeting neurological disorders. Its spirocyclic structure and fluorine substitution make it a valuable scaffold for developing compounds with potential therapeutic effects, such as antipsychotic or antidepressant properties. Researchers often employ it in the design and optimization of drug candidates to enhance their binding affinity and selectivity towards specific receptors in the brain. Additionally, its unique chemical framework allows for further functionalization, enabling the exploration of diverse pharmacological activities.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿178,830.00 |
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tert-Butyl 8'-fluoro-2',4'-dihydro-1'H-spiro[piperidine-4,3'-quinoline]-1-carbox
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of biologically active molecules, particularly those targeting neurological disorders. Its spirocyclic structure and fluorine substitution make it a valuable scaffold for developing compounds with potential therapeutic effects, such as antipsychotic or antidepressant properties. Researchers often employ it in the design and optimization of drug candidates to enhance their binding affinity and selectivity towards specific receptors in the brain. Additionally, its unique chemical framework allows for further functionalization, enabling the exploration of diverse pharmacological activities.
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