8-Bromo-4-chloro-2-(trifluoromethyl)quinoline
≥97%
- Product Code: 173085
CAS:
655235-61-3
| Molecular Weight: | 310.50 g./mol | Molecular Formula: | C₁₀H₄BrClF₃N |
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| EC Number: | MDL Number: | MFCD00174293 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, dry |
Product Description:
Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its halogenated structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. It is also employed in the preparation of bioactive quinoline derivatives with potential antimicrobial and anti-inflammatory properties. Due to the presence of reactive bromo and chloro groups, it serves as a versatile building block in Suzuki, Stille, and Buchwald-Hartwig reactions in drug discovery research.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 250mg | 10-20 days | ฿1,860.00 |
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| 1g | 10-20 days | ฿5,560.00 |
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| 5g | 10-20 days | ฿13,920.00 |
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8-Bromo-4-chloro-2-(trifluoromethyl)quinoline
Used primarily as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its halogenated structure allows for selective cross-coupling reactions, making it valuable in medicinal chemistry for building complex molecules. It is also employed in the preparation of bioactive quinoline derivatives with potential antimicrobial and anti-inflammatory properties. Due to the presence of reactive bromo and chloro groups, it serves as a versatile building block in Suzuki, Stille, and Buchwald-Hartwig reactions in drug discovery research.
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