Ethyl 8-chloro-6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carboxylate
95%
- Product Code: 120431
CAS:
353258-31-8
| Molecular Weight: | 292.64 g./mol | Molecular Formula: | C₁₁H₈ClF₃N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01833013 | |
| Melting Point: | 132-134 °C | Boiling Point: | |
| Density: | 1.50±0.1 g/cm3(Predicted) | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various bioactive molecules, particularly those targeting therapeutic areas such as central nervous system disorders and infectious diseases. Its structural features, including the trifluoromethyl group and imidazopyridine core, make it valuable for designing compounds with enhanced potency and metabolic stability. Researchers often employ it in medicinal chemistry to explore novel drug candidates, leveraging its reactivity and functional groups for further chemical modifications. Additionally, it may be used in the development of agrochemicals, contributing to the creation of new pesticides or herbicides with improved efficacy and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.250 | 10-20 days | $36.63 |
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| 1.000 | 10-20 days | $97.93 |
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| 5.000 | 10-20 days | $344.23 |
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Ethyl 8-chloro-6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carboxylate
This compound is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various bioactive molecules, particularly those targeting therapeutic areas such as central nervous system disorders and infectious diseases. Its structural features, including the trifluoromethyl group and imidazopyridine core, make it valuable for designing compounds with enhanced potency and metabolic stability. Researchers often employ it in medicinal chemistry to explore novel drug candidates, leveraging its reactivity and functional groups for further chemical modifications. Additionally, it may be used in the development of agrochemicals, contributing to the creation of new pesticides or herbicides with improved efficacy and selectivity.
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