tert-butyl 4-[(6-bromopyridin-3-yl)oxy]piperidine-1-carboxylate
≥95%
- Product Code: 238633
CAS:
1823783-13-6
| Molecular Weight: | 357.2428 g./mol | Molecular Formula: | C₁₅H₂₁BrN₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22987895 | |
| Melting Point: | Boiling Point: | 437.8±45.0 °C(Predicted) | |
| Density: | 1.355±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C |
Product Description:
Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex drug candidates. Commonly employed in cross-coupling reactions due to the presence of the bromine moiety, enabling the formation of carbon-carbon and carbon-heteroatom bonds. The tert-butyl carbamate-protected piperidine group provides stability and facilitates further derivatization, useful in multi-step synthetic routes targeting central nervous system agents and anti-inflammatory drugs.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £293.86 |
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| 0.250 | 10-20 days | £587.72 |
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tert-butyl 4-[(6-bromopyridin-3-yl)oxy]piperidine-1-carboxylate
Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex drug candidates. Commonly employed in cross-coupling reactions due to the presence of the bromine moiety, enabling the formation of carbon-carbon and carbon-heteroatom bonds. The tert-butyl carbamate-protected piperidine group provides stability and facilitates further derivatization, useful in multi-step synthetic routes targeting central nervous system agents and anti-inflammatory drugs.
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