Ethyl 6-bromoimidazo[1,2-a]pyridine-2-carboxylate
97%
- Product Code: 61473
CAS:
67625-37-0
| Molecular Weight: | 269.09 g./mol | Molecular Formula: | C₁₀H₉BrN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD06659034 | |
| Melting Point: | 69-72 °C | Boiling Point: | |
| Density: | 1.60±0.1 g/cm3(Predicted) | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Ethyl 6-bromoimidazo[1,2-a]pyridine-2-carboxylate is primarily used in organic synthesis as a versatile intermediate for the development of pharmaceutical compounds. Its structure makes it valuable in the construction of more complex molecules, particularly those with potential biological activity. It is often employed in the synthesis of heterocyclic compounds, which are crucial in drug discovery for treating various diseases. Additionally, it serves as a key building block in the preparation of ligands for medicinal chemistry research, aiding in the exploration of new therapeutic agents. Its bromo group allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for screening purposes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿720.00 |
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| 0.250 | 10-20 days | ฿1,215.00 |
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| 1.000 | 10-20 days | ฿2,385.00 |
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Ethyl 6-bromoimidazo[1,2-a]pyridine-2-carboxylate
Ethyl 6-bromoimidazo[1,2-a]pyridine-2-carboxylate is primarily used in organic synthesis as a versatile intermediate for the development of pharmaceutical compounds. Its structure makes it valuable in the construction of more complex molecules, particularly those with potential biological activity. It is often employed in the synthesis of heterocyclic compounds, which are crucial in drug discovery for treating various diseases. Additionally, it serves as a key building block in the preparation of ligands for medicinal chemistry research, aiding in the exploration of new therapeutic agents. Its bromo group allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for screening purposes.
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