5-(Trifluoromethyl)quinoline-6-carboxylic acid

95%

Reagent Code: #130918
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CAS Number 2703752-33-2

science Other reagents with same CAS 2703752-33-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.17 g/mol
Formula C₁₁H₆F₃NO₂
badge Registry Numbers
MDL Number MFCD34180800
inventory_2 Storage & Handling
Storage Room temperature, away from light, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antimalarial drugs. Its structure supports the creation of bioactive molecules due to the electron-withdrawing trifluoromethyl group and the rigid quinoline core, enhancing metabolic stability and binding affinity. Also employed in agrochemical research for designing novel pesticides with improved efficacy and environmental profiles. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates targeting infectious diseases.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿40,720.00

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5-(Trifluoromethyl)quinoline-6-carboxylic acid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antimalarial drugs. Its structure supports the creation of bioactive molecules due to the electron-withdrawing trifluoromethyl group and the rigid quinoline core, enhancing metabolic stability and binding affinity. Also employed in agrochemical research for designing novel pesticides with improved efficacy and environmental profiles. Commonly utilized in medicinal chemistry for structure-activity r

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antimalarial drugs. Its structure supports the creation of bioactive molecules due to the electron-withdrawing trifluoromethyl group and the rigid quinoline core, enhancing metabolic stability and binding affinity. Also employed in agrochemical research for designing novel pesticides with improved efficacy and environmental profiles. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies to optimize drug candidates targeting infectious diseases.

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