4-Chloro-8-fluoro-2-(trifluoromethyl)quinoline

≥97%

Reagent Code: #173082
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CAS Number 401567-85-9

science Other reagents with same CAS 401567-85-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 249.59 g/mol
Formula C₁₀H₄ClF₄N
badge Registry Numbers
MDL Number MFCD01570536
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of fluorinated quinoline-based pharmaceuticals, particularly in antimalarial and anticancer agents. Its structure supports enhanced bioavailability and binding affinity to target enzymes. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the electron-withdrawing effects of fluorine and chlorine, which influence metabolic stability and lipophilicity. Also utilized in agrochemical research for developing novel pesticides with improved efficacy and environmental profile.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,470.00
inventory 5g
10-20 days ฿7,270.00

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4-Chloro-8-fluoro-2-(trifluoromethyl)quinoline
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Used as a key intermediate in the synthesis of fluorinated quinoline-based pharmaceuticals, particularly in antimalarial and anticancer agents. Its structure supports enhanced bioavailability and binding affinity to target enzymes. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the electron-withdrawing effects of fluorine and chlorine, which influence metabolic stability and lipophilicity. Also utilized in agrochemical research for developing novel pesti

Used as a key intermediate in the synthesis of fluorinated quinoline-based pharmaceuticals, particularly in antimalarial and anticancer agents. Its structure supports enhanced bioavailability and binding affinity to target enzymes. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to the electron-withdrawing effects of fluorine and chlorine, which influence metabolic stability and lipophilicity. Also utilized in agrochemical research for developing novel pesticides with improved efficacy and environmental profile.

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