7-Fluoro-5-methoxyquinoline-3-carboxylic acid

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Reagent Code: #130886
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CAS Number 2828438-97-5

science Other reagents with same CAS 2828438-97-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.18 g/mol
Formula C₁₁H₈FNO₃
thermostat Physical Properties
Boiling Point 373.2±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.404±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of fluorinated quinoline-based pharmaceuticals, particularly in the development of antimalarial and antibacterial agents. Its structure supports the formation of bioactive molecules that interact with pathogen DNA or enzyme targets. Also employed in research for novel kinase inhibitors due to the quinoline core’s affinity for ATP-binding sites in proteins. The fluorine and methoxy groups enhance membrane permeability and metabolic stability in drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿15,110.00
inventory 250mg
10-20 days ฿25,660.00
inventory 1g
10-20 days ฿69,230.00

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7-Fluoro-5-methoxyquinoline-3-carboxylic acid
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Used as a key intermediate in the synthesis of fluorinated quinoline-based pharmaceuticals, particularly in the development of antimalarial and antibacterial agents. Its structure supports the formation of bioactive molecules that interact with pathogen DNA or enzyme targets. Also employed in research for novel kinase inhibitors due to the quinoline core’s affinity for ATP-binding sites in proteins. The fluorine and methoxy groups enhance membrane permeability and metabolic stability in drug candidates.<

Used as a key intermediate in the synthesis of fluorinated quinoline-based pharmaceuticals, particularly in the development of antimalarial and antibacterial agents. Its structure supports the formation of bioactive molecules that interact with pathogen DNA or enzyme targets. Also employed in research for novel kinase inhibitors due to the quinoline core’s affinity for ATP-binding sites in proteins. The fluorine and methoxy groups enhance membrane permeability and metabolic stability in drug candidates.

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