1'-Boc-5-Bromo-1,2-dihydro-2-oxo-spiro[3H-indole-3,4'-piperidine]
95%
- Product Code: 66054
CAS:
873779-30-7
Molecular Weight: | 381.28 g./mol | Molecular Formula: | C₁₇H₂₁BrN₂O₃ |
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EC Number: | MDL Number: | MFCD10566052 | |
Melting Point: | Boiling Point: | 512.1℃ at 760 mmHg | |
Density: | 1.46g/ml | Storage Condition: | Room temperature, dry, sealed |
Product Description:
Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both a Boc-protected amine and a bromo-substituted indole, makes it valuable for constructing complex heterocyclic compounds. It is often employed in the design of potential drug candidates targeting neurological disorders, such as schizophrenia and depression, due to its ability to interact with specific receptors in the brain. Additionally, its spirocyclic framework is utilized in medicinal chemistry to enhance the stability and bioavailability of therapeutic agents. Researchers also leverage its reactivity in cross-coupling reactions to introduce diverse functional groups, enabling the exploration of novel chemical spaces for drug discovery.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.500 | 10-20 days | ฿4,320.00 |
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1.000 | 10-20 days | ฿6,894.00 |
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5.000 | 10-20 days | ฿26,460.00 |
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1'-Boc-5-Bromo-1,2-dihydro-2-oxo-spiro[3H-indole-3,4'-piperidine]
Used primarily in pharmaceutical research and development, this compound serves as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both a Boc-protected amine and a bromo-substituted indole, makes it valuable for constructing complex heterocyclic compounds. It is often employed in the design of potential drug candidates targeting neurological disorders, such as schizophrenia and depression, due to its ability to interact with specific receptors in the brain. Additionally, its spirocyclic framework is utilized in medicinal chemistry to enhance the stability and bioavailability of therapeutic agents. Researchers also leverage its reactivity in cross-coupling reactions to introduce diverse functional groups, enabling the exploration of novel chemical spaces for drug discovery.
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