2-(Trifluoromethyl)quinolin-7-ol

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Reagent Code: #238365
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CAS Number 41192-81-8

science Other reagents with same CAS 41192-81-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.15 g/mol
Formula C₁₀H₆NOF₃
badge Registry Numbers
MDL Number MFCD02192593
inventory_2 Storage & Handling
Storage Room temperature, seal, 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 kinase inhibitors due to the electron-withdrawing trifluoromethyl group enhancing metabolic stability and binding affinity. Also employed in agrochemicals for crop protection, where it contributes to improved environmental persistence and biological activity. Additionally, it serves as a building block in materials science for designing fluorinated organic semiconductors with enhanced thermal and oxidative stability.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿18,840.00
inventory 250mg
10-20 days ฿32,020.00

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2-(Trifluoromethyl)quinolin-7-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 kinase inhibitors due to the electron-withdrawing trifluoromethyl group enhancing metabolic stability and binding affinity. Also employed in agrochemicals for crop protection, where it contributes to improved environmental persistence and biological activity. Additionally, it serves as a building block in materials science for designing fluorinated

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in antimalarial and anticancer agents. Its structure supports the development of kinase inhibitors due to the electron-withdrawing trifluoromethyl group enhancing metabolic stability and binding affinity. Also employed in agrochemicals for crop protection, where it contributes to improved environmental persistence and biological activity. Additionally, it serves as a building block in materials science for designing fluorinated organic semiconductors with enhanced thermal and oxidative stability.

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