tert-Butyl 5-bromospiro[indoline-3,4'-piperidine]-1'-carboxylate
95%
- Product Code: 76023
CAS:
878167-55-6
| Molecular Weight: | 367.29 g./mol | Molecular Formula: | C₁₇H₂₃BrN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD10696106 | |
| Melting Point: | Boiling Point: | 463.58ºC at 760 mmHg | |
| Density: | 1.395g/ml | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This chemical is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of complex organic molecules. It serves as a key intermediate in the creation of various biologically active compounds, including potential drug candidates. Its structure, featuring a spirocyclic indoline-piperidine framework, makes it valuable for constructing molecules with specific stereochemical properties, which are crucial for targeting certain biological pathways. Researchers often employ it in the development of central nervous system (CNS) drugs, as its scaffold can interact with receptors and enzymes in the brain. Additionally, its bromo substituent allows for further functionalization through cross-coupling reactions, enabling the creation of diverse derivatives for medicinal chemistry studies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $2,693.04 |
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| 1.000 | 10-20 days | $6,427.44 |
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tert-Butyl 5-bromospiro[indoline-3,4'-piperidine]-1'-carboxylate
This chemical is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of complex organic molecules. It serves as a key intermediate in the creation of various biologically active compounds, including potential drug candidates. Its structure, featuring a spirocyclic indoline-piperidine framework, makes it valuable for constructing molecules with specific stereochemical properties, which are crucial for targeting certain biological pathways. Researchers often employ it in the development of central nervous system (CNS) drugs, as its scaffold can interact with receptors and enzymes in the brain. Additionally, its bromo substituent allows for further functionalization through cross-coupling reactions, enabling the creation of diverse derivatives for medicinal chemistry studies.
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