Ethyl 4-chloro-5,7-dimethylquinoline-3-carboxylate
95%
- Product Code: 47161
CAS:
338954-49-7
| Molecular Weight: | 263.7200 g./mol | Molecular Formula: | C₁₄H₁₄ClNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00173354 | |
| Melting Point: | Boiling Point: | 363.3 °C at 760 mmHg | |
| Density: | 1.222g/cm3 | Storage Condition: | room temperature |
Product Description:
Ethyl 4-chloro-5,7-dimethylquinoline-3-carboxylate is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. Its quinoline core structure makes it a valuable scaffold for developing pharmaceuticals, particularly in the design of antimalarial and anticancer agents. Researchers leverage its chemical framework to create derivatives that can interact with specific biological targets, such as enzymes or receptors, to modulate disease pathways. Additionally, it finds application in organic synthesis for constructing complex molecules due to its reactive functional groups, which allow for further chemical modifications. Its role in drug discovery and development highlights its importance in advancing therapeutic innovations.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿5,490.00 |
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Ethyl 4-chloro-5,7-dimethylquinoline-3-carboxylate
Ethyl 4-chloro-5,7-dimethylquinoline-3-carboxylate is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various biologically active compounds. Its quinoline core structure makes it a valuable scaffold for developing pharmaceuticals, particularly in the design of antimalarial and anticancer agents. Researchers leverage its chemical framework to create derivatives that can interact with specific biological targets, such as enzymes or receptors, to modulate disease pathways. Additionally, it finds application in organic synthesis for constructing complex molecules due to its reactive functional groups, which allow for further chemical modifications. Its role in drug discovery and development highlights its importance in advancing therapeutic innovations.
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