tert-Butyl7-fluoro-2-oxo-1,2-dihydrospiro[indole-3,4'-piperidine]-1'-carboxylate
97%
- Product Code: 75940
CAS:
1290626-82-2
| Molecular Weight: | 320 g./mol | Molecular Formula: | C₁₇H₂₁FN₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD19442319 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive compounds. Its unique structure, featuring a spirocyclic indole-piperidine framework, makes it valuable for developing molecules with potential therapeutic applications. It is often employed in the research and development of drugs targeting neurological disorders, such as depression, anxiety, and schizophrenia, due to its ability to interact with specific receptors in the brain. Additionally, its fluoro and carbonyl functional groups enhance its reactivity, enabling its use in the creation of complex chemical entities for drug discovery programs. Its role in medicinal chemistry is significant, particularly in optimizing the pharmacokinetic and pharmacodynamic properties of lead compounds.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.025 | 10-20 days | ฿2,700.00 |
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| 0.100 | 10-20 days | ฿9,490.00 |
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| 0.250 | 10-20 days | ฿19,520.00 |
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| 1.000 | 10-20 days | ฿41,390.00 |
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tert-Butyl7-fluoro-2-oxo-1,2-dihydrospiro[indole-3,4'-piperidine]-1'-carboxylate
This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive compounds. Its unique structure, featuring a spirocyclic indole-piperidine framework, makes it valuable for developing molecules with potential therapeutic applications. It is often employed in the research and development of drugs targeting neurological disorders, such as depression, anxiety, and schizophrenia, due to its ability to interact with specific receptors in the brain. Additionally, its fluoro and carbonyl functional groups enhance its reactivity, enabling its use in the creation of complex chemical entities for drug discovery programs. Its role in medicinal chemistry is significant, particularly in optimizing the pharmacokinetic and pharmacodynamic properties of lead compounds.
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