2-(4-Bromophenyl)-1-(piperidin-1-yl)ethan-1-one
≥95%
- Product Code: 141721
CAS:
349430-81-5
| Molecular Weight: | 282.1762 g./mol | Molecular Formula: | C₁₃H₁₆BrNO |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | 417.5±28.0 °C(Predicted) | |
| Density: | 1.372±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C |
Product Description:
Used as an intermediate in organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a building block for creating bioactive molecules due to the presence of both the aromatic bromo substituent and the piperidine moiety, which are common structural elements in drug design. The compound is employed in cross-coupling reactions, such as Suzuki or Heck reactions, enabling the formation of complex aromatic systems. It also finds use in the synthesis of central nervous system agents, where the piperidine ring contributes to blood-brain barrier penetration. Its ketone functionality allows for further functionalization, such as reduction or imine formation, supporting its role in multi-step synthetic routes.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿28,800.00 |
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| 0.250 | 10-20 days | ฿48,000.00 |
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| 1.000 | 10-20 days | ฿96,000.00 |
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2-(4-Bromophenyl)-1-(piperidin-1-yl)ethan-1-one
Used as an intermediate in organic synthesis, particularly in the development of pharmaceutical compounds. It serves as a building block for creating bioactive molecules due to the presence of both the aromatic bromo substituent and the piperidine moiety, which are common structural elements in drug design. The compound is employed in cross-coupling reactions, such as Suzuki or Heck reactions, enabling the formation of complex aromatic systems. It also finds use in the synthesis of central nervous system agents, where the piperidine ring contributes to blood-brain barrier penetration. Its ketone functionality allows for further functionalization, such as reduction or imine formation, supporting its role in multi-step synthetic routes.
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