6-Bromo-3-fluoroquinoline
95%
- Product Code: 87659
CAS:
1355583-13-9
| Molecular Weight: | 226.05 g./mol | Molecular Formula: | C₉H₅BrFN |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22690571 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
Product Description:
6-Bromo-3-fluoroquinoline is primarily used in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active compounds. Its structure is particularly valuable in the creation of quinoline-based drugs, which are known for their broad therapeutic applications. The compound is often utilized in the design of antimicrobial and anticancer agents due to the inherent biological activity of the quinoline scaffold. Additionally, it serves as a building block in the development of fluorescent probes and imaging agents, aiding in the study of cellular processes and disease mechanisms. Its halogenated nature allows for further chemical modifications, making it a versatile component in medicinal chemistry and drug discovery efforts.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿12,744.00 |
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| 0.250 | 10-20 days | ฿19,080.00 |
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6-Bromo-3-fluoroquinoline
6-Bromo-3-fluoroquinoline is primarily used in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active compounds. Its structure is particularly valuable in the creation of quinoline-based drugs, which are known for their broad therapeutic applications. The compound is often utilized in the design of antimicrobial and anticancer agents due to the inherent biological activity of the quinoline scaffold. Additionally, it serves as a building block in the development of fluorescent probes and imaging agents, aiding in the study of cellular processes and disease mechanisms. Its halogenated nature allows for further chemical modifications, making it a versatile component in medicinal chemistry and drug discovery efforts.
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