Ethyl 4-chloro-8-fluoroquinoline-3-carboxylate
98%
- Product Code: 47234
CAS:
56824-90-9
| Molecular Weight: | 253.6600 g./mol | Molecular Formula: | C₁₂H₉ClFNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00173364 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the pharmaceutical and chemical research sectors as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both chloro and fluoro substituents on the quinoline ring, makes it a valuable precursor for developing drugs, particularly antibiotics and antimicrobial agents. Researchers often employ it in the creation of quinolone derivatives, which are known for their efficacy in treating bacterial infections. Additionally, its carboxylate group allows for further functionalization, enabling the production of compounds with potential therapeutic applications in areas such as cancer treatment and anti-inflammatory drugs. Its role in medicinal chemistry underscores its importance in advancing drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,430.00 |
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Ethyl 4-chloro-8-fluoroquinoline-3-carboxylate
This compound is primarily utilized in the pharmaceutical and chemical research sectors as a key intermediate in the synthesis of various biologically active molecules. Its structure, featuring both chloro and fluoro substituents on the quinoline ring, makes it a valuable precursor for developing drugs, particularly antibiotics and antimicrobial agents. Researchers often employ it in the creation of quinolone derivatives, which are known for their efficacy in treating bacterial infections. Additionally, its carboxylate group allows for further functionalization, enabling the production of compounds with potential therapeutic applications in areas such as cancer treatment and anti-inflammatory drugs. Its role in medicinal chemistry underscores its importance in advancing drug discovery and development.
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