tert-Butyl 7-bromo-2-oxo-1,2-dihydrospiro[indole-3,4'-piperidine]-1'-carboxylate
95%
- Product Code: 67930
CAS:
1779125-91-5
| Molecular Weight: | 381.26 g./mol | Molecular Formula: | C₁₇H₂₁BrN₂O₃ |
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| EC Number: | MDL Number: | MFCD27995806 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of complex organic molecules. Its structure, featuring a spirocyclic indole and piperidine moiety, makes it valuable for constructing biologically active compounds, particularly in the design of potential drug candidates targeting neurological disorders or cancer. The presence of the bromo substituent allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for biological screening. Additionally, the tert-butyloxycarbonyl (Boc) protecting group enhances its stability during synthetic processes, facilitating its use in multi-step organic syntheses. Its applications are particularly significant in medicinal chemistry for exploring novel therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿184,860.00 |
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tert-Butyl 7-bromo-2-oxo-1,2-dihydrospiro[indole-3,4'-piperidine]-1'-carboxylate
This compound is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of complex organic molecules. Its structure, featuring a spirocyclic indole and piperidine moiety, makes it valuable for constructing biologically active compounds, particularly in the design of potential drug candidates targeting neurological disorders or cancer. The presence of the bromo substituent allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for biological screening. Additionally, the tert-butyloxycarbonyl (Boc) protecting group enhances its stability during synthetic processes, facilitating its use in multi-step organic syntheses. Its applications are particularly significant in medicinal chemistry for exploring novel therapeutic agents.
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