Ethyl 7-bromoimidazo[1,2-a]pyridine-2-carboxylate
98%
- Product Code: 84145
CAS:
1187236-18-5
Molecular Weight: | 269.10 g./mol | Molecular Formula: | C₁₀H₉BrN₂O₂ |
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EC Number: | MDL Number: | MFCD11505036 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C, dry, airtight |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the development of more complex molecules. Its structure, featuring a bromine atom and an ester group, makes it a versatile building block for constructing various heterocyclic compounds. These heterocycles are often explored for their potential biological activities, including applications in pharmaceuticals. Researchers frequently employ this chemical in the synthesis of drug candidates, particularly those targeting neurological disorders or infections, due to the imidazopyridine core's relevance in medicinal chemistry. Additionally, its reactivity allows for further functionalization, enabling the creation of diverse chemical libraries for screening and discovery purposes.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | $56.71 |
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1.000 | 10-20 days | $90.46 |
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5.000 | 10-20 days | $270.57 |
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Ethyl 7-bromoimidazo[1,2-a]pyridine-2-carboxylate
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the development of more complex molecules. Its structure, featuring a bromine atom and an ester group, makes it a versatile building block for constructing various heterocyclic compounds. These heterocycles are often explored for their potential biological activities, including applications in pharmaceuticals. Researchers frequently employ this chemical in the synthesis of drug candidates, particularly those targeting neurological disorders or infections, due to the imidazopyridine core's relevance in medicinal chemistry. Additionally, its reactivity allows for further functionalization, enabling the creation of diverse chemical libraries for screening and discovery purposes.
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