tert-Butyl 6-bromo-4H-spiro[benzo[d][1,3]-dioxine-2,4'-piperidine]-1'-carboxylate
95%
- Product Code: 75729
CAS:
895525-73-2
| Molecular Weight: | 384.28 g./mol | Molecular Formula: | C₁₇H₂₂BrNO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD13195393 | |
| Melting Point: | Boiling Point: | 474.441℃ at 760 mmHg | |
| Density: | 1.434 g/ml | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
This compound is primarily utilized in organic synthesis as an intermediate for the development of more complex molecules, particularly in pharmaceutical research. It serves as a key building block in the synthesis of various biologically active compounds, including potential drug candidates. The spirocyclic structure and functional groups present in the molecule make it valuable for constructing diverse chemical architectures, especially in the design of central nervous system (CNS) targeting drugs. It is also employed in medicinal chemistry for exploring structure-activity relationships (SAR) to optimize drug efficacy and selectivity. Additionally, its bromo group allows for further functionalization through cross-coupling reactions, enabling the creation of novel derivatives for biological evaluation.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿8,082.00 |
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| 1.000 | 10-20 days | ฿16,182.00 |
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tert-Butyl 6-bromo-4H-spiro[benzo[d][1,3]-dioxine-2,4'-piperidine]-1'-carboxylate
This compound is primarily utilized in organic synthesis as an intermediate for the development of more complex molecules, particularly in pharmaceutical research. It serves as a key building block in the synthesis of various biologically active compounds, including potential drug candidates. The spirocyclic structure and functional groups present in the molecule make it valuable for constructing diverse chemical architectures, especially in the design of central nervous system (CNS) targeting drugs. It is also employed in medicinal chemistry for exploring structure-activity relationships (SAR) to optimize drug efficacy and selectivity. Additionally, its bromo group allows for further functionalization through cross-coupling reactions, enabling the creation of novel derivatives for biological evaluation.
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