Methyl 8-bromoimidazo[1,2-a]pyridine-6-carboxylate
96%
- Product Code: 52795
CAS:
1234616-08-0
| Molecular Weight: | 255.0700 g./mol | Molecular Formula: | C₉H₇BrN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD17016026 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring both a bromo and an ester functional group, makes it a versatile building block in pharmaceutical research. It is often employed in the synthesis of biologically active compounds, particularly those targeting neurological disorders, due to the imidazopyridine core's relevance in medicinal chemistry. Additionally, it serves as a precursor in the creation of heterocyclic compounds, which are widely explored for their potential therapeutic applications, such as anti-inflammatory, antimicrobial, and anticancer agents. Its reactivity allows for further functionalization, enabling the construction of diverse chemical libraries for drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | £38.88 |
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Methyl 8-bromoimidazo[1,2-a]pyridine-6-carboxylate
This compound is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring both a bromo and an ester functional group, makes it a versatile building block in pharmaceutical research. It is often employed in the synthesis of biologically active compounds, particularly those targeting neurological disorders, due to the imidazopyridine core's relevance in medicinal chemistry. Additionally, it serves as a precursor in the creation of heterocyclic compounds, which are widely explored for their potential therapeutic applications, such as anti-inflammatory, antimicrobial, and anticancer agents. Its reactivity allows for further functionalization, enabling the construction of diverse chemical libraries for drug discovery.
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