6-Bromo-4-chloro-7-methoxyquinoline

98%

Reagent Code: #145495
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CAS Number 476660-71-6

science Other reagents with same CAS 476660-71-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 272.53 g/mol
Formula C₁₀H₇BrClNO
thermostat Physical Properties
Boiling Point 348.9±37.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its halogen and methoxy functional groups allow selective modifications for building complex drug molecules. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig to introduce aromatic amines or other pharmacophores. Also utilized in agrochemical research for designing bioactive molecules with improved stability and target specificity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿950.00
inventory 1g
10-20 days ฿2,020.00
inventory 5g
10-20 days ฿9,560.00

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6-Bromo-4-chloro-7-methoxyquinoline
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Used as a key intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its halogen and methoxy functional groups allow selective modifications for building complex drug molecules. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig to introduce aromatic amines or other pharmacophores. Also utilized in agrochemical research for designing bioactive molecules with improved stability and target specif

Used as a key intermediate in the synthesis of quinoline-based pharmaceuticals, particularly in the development of antimalarial and anticancer agents. Its halogen and methoxy functional groups allow selective modifications for building complex drug molecules. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig to introduce aromatic amines or other pharmacophores. Also utilized in agrochemical research for designing bioactive molecules with improved stability and target specificity.

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