5-Bromo-8-(difluoromethoxy)quinoline
95%
- Product Code: 126263
CAS:
199872-10-1
| Molecular Weight: | 274.06 g./mol | Molecular Formula: | C10H6BrF2NO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28658264 | |
| Melting Point: | Boiling Point: | 332.2±37.0 °C(Predicted) | |
| Density: | 1.629±0.06 g/cm3(Predicted) | Storage Condition: | room temperature, inert atmosphere |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its unique structure, featuring a quinoline core with bromo and difluoromethoxy substituents, makes it valuable for developing compounds with potential biological activity. It is often explored in the design of drugs targeting infectious diseases, particularly those caused by bacteria or parasites, due to its ability to interfere with microbial enzymes or DNA replication. Additionally, it serves as a building block in the creation of fluorescent probes or imaging agents for research purposes, leveraging its aromatic system for light absorption and emission properties. Its application extends to material science, where it can be incorporated into organic electronic materials for its electron-rich characteristics.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $580.06 |
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| 1.000 | 10-20 days | $2,753.61 |
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5-Bromo-8-(difluoromethoxy)quinoline
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its unique structure, featuring a quinoline core with bromo and difluoromethoxy substituents, makes it valuable for developing compounds with potential biological activity. It is often explored in the design of drugs targeting infectious diseases, particularly those caused by bacteria or parasites, due to its ability to interfere with microbial enzymes or DNA replication. Additionally, it serves as a building block in the creation of fluorescent probes or imaging agents for research purposes, leveraging its aromatic system for light absorption and emission properties. Its application extends to material science, where it can be incorporated into organic electronic materials for its electron-rich characteristics.
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