5-bromoimidazo[1,5-a]pyridine-1-carboxylate
95%
- Product Code: 87616
CAS:
1330766-11-4
| Molecular Weight: | 269.1 g./mol | Molecular Formula: | C₁₀H₉BrN₂O₂ |
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| EC Number: | MDL Number: | MFCD20231092 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex molecules. Its structure is particularly valuable in the construction of heterocyclic compounds, which are often explored for their potential pharmacological activities. Researchers leverage this compound in the synthesis of novel drug candidates, especially those targeting neurological disorders and cancer, due to its imidazopyridine core, which is a common motif in bioactive molecules. Additionally, it is employed in the preparation of ligands for metal-catalyzed reactions, aiding in the discovery of new catalytic processes. Its bromo substituent also makes it a useful building block 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 | €601.91 |
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| 0.250 | 10-20 days | €1,124.27 |
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5-bromoimidazo[1,5-a]pyridine-1-carboxylate
This chemical is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex molecules. Its structure is particularly valuable in the construction of heterocyclic compounds, which are often explored for their potential pharmacological activities. Researchers leverage this compound in the synthesis of novel drug candidates, especially those targeting neurological disorders and cancer, due to its imidazopyridine core, which is a common motif in bioactive molecules. Additionally, it is employed in the preparation of ligands for metal-catalyzed reactions, aiding in the discovery of new catalytic processes. Its bromo substituent also makes it a useful building block for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical libraries for screening purposes.
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