Ethyl 4-hydroxy-6-(trifluoromethoxy)quinoline-3-carboxylate
≥95%
- Product Code: 47833
CAS:
175203-85-7
| Molecular Weight: | 301.22 g./mol | Molecular Formula: | C₁₃H₁₀F₃NO₄ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00219847 | |
| Melting Point: | Boiling Point: | 357.3°C at 760 mmHg | |
| Density: | Storage Condition: | room temperature, stored under inert gas |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a quinoline core with trifluoromethoxy and ester functional groups, makes it a versatile building block for developing potential pharmaceutical agents. It is particularly explored in the design of compounds targeting neurological disorders, inflammation, and infectious diseases due to its ability to interact with specific biological targets. Additionally, its trifluoromethoxy group enhances metabolic stability and bioavailability, making it valuable in drug discovery and development processes. Researchers also investigate its potential as a precursor for creating fluorescent probes or imaging agents in biochemical studies.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿288.00 |
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| 5.000 | 10-20 days | ฿1,341.00 |
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| 10.000 | 10-20 days | ฿2,592.00 |
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| 25.000 | 10-20 days | ฿5,175.00 |
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Ethyl 4-hydroxy-6-(trifluoromethoxy)quinoline-3-carboxylate
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a quinoline core with trifluoromethoxy and ester functional groups, makes it a versatile building block for developing potential pharmaceutical agents. It is particularly explored in the design of compounds targeting neurological disorders, inflammation, and infectious diseases due to its ability to interact with specific biological targets. Additionally, its trifluoromethoxy group enhances metabolic stability and bioavailability, making it valuable in drug discovery and development processes. Researchers also investigate its potential as a precursor for creating fluorescent probes or imaging agents in biochemical studies.
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