tert-Butyl 7-bromo-3-oxo-2,3-dihydrospiro[indene-1,4'-piperidine]-1'-carboxylate
≥95%
- Product Code: 151189
CAS:
1160247-52-8
| Molecular Weight: | 380.28 g./mol | Molecular Formula: | C₁₈H₂₂BrNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12198608 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry, sealed |
Product Description:
Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) active compounds. Its spirocyclic structure and functional groups make it valuable for constructing complex piperidine-based scaffolds found in bioactive molecules. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies, especially in the design of receptor modulators. The bromo substituent allows for further functionalization via cross-coupling reactions, enabling rapid diversification in drug discovery programs. Also utilized in the preparation of selective enzyme inhibitors and neuroactive agents due to its conformational rigidity and favorable pharmacokinetic properties.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿23,000.00 |
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| 250mg | 10-20 days | ฿40,240.00 |
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| 1g | 10-20 days | ฿80,490.00 |
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tert-Butyl 7-bromo-3-oxo-2,3-dihydrospiro[indene-1,4'-piperidine]-1'-carboxylate
Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of central nervous system (CNS) active compounds. Its spirocyclic structure and functional groups make it valuable for constructing complex piperidine-based scaffolds found in bioactive molecules. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies, especially in the design of receptor modulators. The bromo substituent allows for further functionalization via cross-coupling reactions, enabling rapid diversification in drug discovery programs. Also utilized in the preparation of selective enzyme inhibitors and neuroactive agents due to its conformational rigidity and favorable pharmacokinetic properties.
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