Ethyl 6-fluoroimidazo[1,2-a]pyridine-3-carboxylate
97%
- Product Code: 120484
CAS:
1359655-87-0
| Molecular Weight: | 208.19 g./mol | Molecular Formula: | C₁₀H₉FN₂O₂ |
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| EC Number: | MDL Number: | MFCD21364586 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
Ethyl 6-fluoroimidazo[1,2-a]pyridine-3-carboxylate is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active compounds. Its structure is particularly valuable in the creation of molecules with potential therapeutic applications, such as anti-inflammatory, antimicrobial, or anticancer agents. The compound’s imidazopyridine core is often explored for its ability to interact with biological targets, including enzymes and receptors, making it a versatile building block in drug discovery. Additionally, its fluorine substitution enhances its metabolic stability and binding affinity, which is advantageous in optimizing drug candidates for improved efficacy and safety. Researchers also investigate its role in developing novel treatments for neurological disorders due to its potential to cross the blood-brain barrier.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $21.06 |
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| 0.250 | 10-20 days | $34.29 |
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| 1.000 | 10-20 days | $85.87 |
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| 5.000 | 10-20 days | $274.08 |
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Ethyl 6-fluoroimidazo[1,2-a]pyridine-3-carboxylate
Ethyl 6-fluoroimidazo[1,2-a]pyridine-3-carboxylate is primarily utilized in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active compounds. Its structure is particularly valuable in the creation of molecules with potential therapeutic applications, such as anti-inflammatory, antimicrobial, or anticancer agents. The compound’s imidazopyridine core is often explored for its ability to interact with biological targets, including enzymes and receptors, making it a versatile building block in drug discovery. Additionally, its fluorine substitution enhances its metabolic stability and binding affinity, which is advantageous in optimizing drug candidates for improved efficacy and safety. Researchers also investigate its role in developing novel treatments for neurological disorders due to its potential to cross the blood-brain barrier.
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