Ethyl 7-bromo-4-oxo-1,4-dihydroquinoline-3-carboxylate
95%
- Product Code: 51091
CAS:
208580-23-8
Molecular Weight: | 296.12 g./mol | Molecular Formula: | C₁₂H₁₀BrNO₃ |
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Density: | Storage Condition: | room temperature |
Product Description:
Ethyl 7-bromo-4-oxo-1,4-dihydroquinoline-3-carboxylate is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. Its structure is particularly valuable in the development of quinoline-based derivatives, which are known for their broad spectrum of pharmacological properties. This compound is often employed in the creation of potential antimicrobial, anticancer, and anti-inflammatory agents due to the versatility of the quinoline scaffold. Additionally, it serves as a building block in organic synthesis, enabling researchers to explore and optimize new drug candidates with enhanced efficacy and selectivity. Its bromo and ester functional groups make it a versatile precursor for further chemical modifications, facilitating the discovery of novel therapeutic molecules.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.050 | 10-20 days | ฿4,230.00 |
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Ethyl 7-bromo-4-oxo-1,4-dihydroquinoline-3-carboxylate
Ethyl 7-bromo-4-oxo-1,4-dihydroquinoline-3-carboxylate is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. Its structure is particularly valuable in the development of quinoline-based derivatives, which are known for their broad spectrum of pharmacological properties. This compound is often employed in the creation of potential antimicrobial, anticancer, and anti-inflammatory agents due to the versatility of the quinoline scaffold. Additionally, it serves as a building block in organic synthesis, enabling researchers to explore and optimize new drug candidates with enhanced efficacy and selectivity. Its bromo and ester functional groups make it a versatile precursor for further chemical modifications, facilitating the discovery of novel therapeutic molecules.
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