4-Bromo-8-fluoroquinoline
≥95%
- Product Code: 79521
CAS:
927800-38-2
| Molecular Weight: | 226.05 g./mol | Molecular Formula: | C₉H₅BrFN |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07700231 | |
| Melting Point: | Boiling Point: | 299.7°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
4-Bromo-8-fluoroquinoline is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those with potential antibacterial, antifungal, and anticancer properties. The presence of both bromine and fluorine atoms in the quinoline structure enhances its reactivity, making it a valuable building block for modifying and optimizing drug candidates. Researchers often employ it to develop novel quinoline-based derivatives, which are then screened for therapeutic efficacy. Additionally, it is used in the study of structure-activity relationships (SAR) to understand how specific substituents influence the biological activity of quinoline compounds. Its applications also extend to material science, where it can be incorporated into organic electronic materials for advanced technological applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿2,682.00 |
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| 1.000 | 10-20 days | ฿6,714.00 |
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| 5.000 | 10-20 days | ฿20,214.00 |
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4-Bromo-8-fluoroquinoline
4-Bromo-8-fluoroquinoline is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those with potential antibacterial, antifungal, and anticancer properties. The presence of both bromine and fluorine atoms in the quinoline structure enhances its reactivity, making it a valuable building block for modifying and optimizing drug candidates. Researchers often employ it to develop novel quinoline-based derivatives, which are then screened for therapeutic efficacy. Additionally, it is used in the study of structure-activity relationships (SAR) to understand how specific substituents influence the biological activity of quinoline compounds. Its applications also extend to material science, where it can be incorporated into organic electronic materials for advanced technological applications.
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