tert-Butyl 6-bromo-4-oxospiro[chroman-2,4'-piperidine]-1'-carboxylate
95%
- Product Code: 76027
CAS:
690632-38-3
| Molecular Weight: | 396.29 g./mol | Molecular Formula: | C₁₈H₂₂BrNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD05865132 | |
| Melting Point: | Boiling Point: | 501.3±50.0℃ at 760 mmHg | |
| Density: | 1.44g/ml | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of complex organic molecules. It serves as a key intermediate in the production of biologically active compounds, especially those targeting central nervous system disorders. Its structural features, including the spirocyclic and piperidine moieties, make it valuable for designing molecules with potential therapeutic effects. Researchers often employ it in medicinal chemistry to explore novel drug candidates, optimize pharmacokinetic properties, and enhance binding affinity to specific biological targets. Additionally, its bromo and carboxylate functional groups allow for further chemical modifications, enabling the creation of diverse derivatives for screening and evaluation in drug discovery programs.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿10,818.00 |
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| 5.000 | 10-20 days | ฿30,249.00 |
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tert-Butyl 6-bromo-4-oxospiro[chroman-2,4'-piperidine]-1'-carboxylate
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of complex organic molecules. It serves as a key intermediate in the production of biologically active compounds, especially those targeting central nervous system disorders. Its structural features, including the spirocyclic and piperidine moieties, make it valuable for designing molecules with potential therapeutic effects. Researchers often employ it in medicinal chemistry to explore novel drug candidates, optimize pharmacokinetic properties, and enhance binding affinity to specific biological targets. Additionally, its bromo and carboxylate functional groups allow for further chemical modifications, enabling the creation of diverse derivatives for screening and evaluation in drug discovery programs.
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