6-Fluoro-3-oxo-2,3-dihydrospiro[indene-1,4'-piperidine]-1'-carboxylic acid tert-butyl ester
97%
- Product Code: 75702
CAS:
910442-55-6
| Molecular Weight: | 319.38 g./mol | Molecular Formula: | C₁₈H₂₂FNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08460788 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of biologically active molecules. Its structure, featuring a spirocyclic system and a fluorine atom, makes it valuable for developing compounds with potential therapeutic effects. It is often employed in the research and development of drugs targeting neurological disorders, such as anxiety, depression, or neurodegenerative diseases, due to its ability to interact with specific receptors in the brain. Additionally, its tert-butyl ester group enhances its stability, making it suitable for further chemical modifications during drug synthesis. Researchers also explore its use in creating novel compounds with anti-inflammatory or analgesic properties, leveraging its unique chemical framework.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿68,210.00 |
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| 0.500 | 10-20 days | ฿96,520.00 |
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6-Fluoro-3-oxo-2,3-dihydrospiro[indene-1,4'-piperidine]-1'-carboxylic acid tert-butyl ester
This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of biologically active molecules. Its structure, featuring a spirocyclic system and a fluorine atom, makes it valuable for developing compounds with potential therapeutic effects. It is often employed in the research and development of drugs targeting neurological disorders, such as anxiety, depression, or neurodegenerative diseases, due to its ability to interact with specific receptors in the brain. Additionally, its tert-butyl ester group enhances its stability, making it suitable for further chemical modifications during drug synthesis. Researchers also explore its use in creating novel compounds with anti-inflammatory or analgesic properties, leveraging its unique chemical framework.
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