tert-Butyl 6-bromospiro[chromane-2,4'-piperidine]-1'-carboxylate
97%
- Product Code: 150823
CAS:
1194374-64-5
| Molecular Weight: | 382.29 g./mol | Molecular Formula: | C₁₈H₂₄BrNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11227132 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature |
Product Description:
Used as an intermediate in pharmaceutical synthesis, particularly in the development of central nervous system agents. Its spirocyclic structure and functional groups make it valuable for constructing complex piperidine-based drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the stability imparted by the tert-butoxycarbonyl (Boc) protecting group. The bromine atom allows for further functionalization via cross-coupling reactions such as Suzuki or Buchwald-Hartwig, enabling rapid diversification in lead optimization. Also utilized in the preparation of selective enzyme inhibitors and receptor modulators.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿10,550.00 |
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| 250mg | 10-20 days | ฿19,210.00 |
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| 1g | 10-20 days | ฿36,150.00 |
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tert-Butyl 6-bromospiro[chromane-2,4'-piperidine]-1'-carboxylate
Used as an intermediate in pharmaceutical synthesis, particularly in the development of central nervous system agents. Its spirocyclic structure and functional groups make it valuable for constructing complex piperidine-based drug candidates. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the stability imparted by the tert-butoxycarbonyl (Boc) protecting group. The bromine atom allows for further functionalization via cross-coupling reactions such as Suzuki or Buchwald-Hartwig, enabling rapid diversification in lead optimization. Also utilized in the preparation of selective enzyme inhibitors and receptor modulators.
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