2-(Trifluoromethyl)quinolin-4-ol

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Reagent Code: #240677
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CAS Number 1701-18-4

science Other reagents with same CAS 1701-18-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.16 g/mol
Formula C₁₀H₆F₃NO
badge Registry Numbers
MDL Number MFCD00153196
thermostat Physical Properties
Melting Point 209-211°C
Boiling Point 220.8°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in antimalarial and anticancer agents. Its structure supports the development of bioactive molecules due to the presence of both quinoline core and trifluoromethyl group, which enhance metabolic stability and membrane permeability. Also employed in agrochemicals for crop protection, where it contributes to improved efficacy and environmental stability of active ingredients. Additionally, it serves as a building block in materials science for designing fluorescent probes and optoelectronic materials owing to its electron-withdrawing properties and rigid aromatic framework.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿820.00
inventory 25g
10-20 days ฿3,860.00
inventory 100g
10-20 days ฿15,180.00
inventory 500g
10-20 days ฿71,950.00

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2-(Trifluoromethyl)quinolin-4-ol
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in antimalarial and anticancer agents. Its structure supports the development of bioactive molecules due to the presence of both quinoline core and trifluoromethyl group, which enhance metabolic stability and membrane permeability. Also employed in agrochemicals for crop protection, where it contributes to improved efficacy and environmental stability of active ingredients. Additionally, it serves as a building block in materials s
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in antimalarial and anticancer agents. Its structure supports the development of bioactive molecules due to the presence of both quinoline core and trifluoromethyl group, which enhance metabolic stability and membrane permeability. Also employed in agrochemicals for crop protection, where it contributes to improved efficacy and environmental stability of active ingredients. Additionally, it serves as a building block in materials science for designing fluorescent probes and optoelectronic materials owing to its electron-withdrawing properties and rigid aromatic framework.
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