4-Nitro-2-(Trifluoromethoxy)Anisole

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Reagent Code: #123918
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CAS Number 647855-18-3

science Other reagents with same CAS 647855-18-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.13 g/mol
Formula C₈H₆F₃NO₄
badge Registry Numbers
MDL Number MFCD18399920
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used primarily in the synthesis of advanced organic compounds, it serves as a key intermediate in the production of agrochemicals and pharmaceuticals. Its unique structure, featuring nitro and trifluoromethoxy groups, makes it valuable in developing herbicides and pesticides, where it enhances efficacy and selectivity. Additionally, it is employed in research settings to study chemical reactions involving electron-withdrawing groups, aiding in the design of novel materials and active ingredients. Its application in medicinal chemistry includes the development of potential drug candidates targeting specific biological pathways.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿32,670.00
inventory 250mg
10-20 days ฿16,371.00

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4-Nitro-2-(Trifluoromethoxy)Anisole
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Used primarily in the synthesis of advanced organic compounds, it serves as a key intermediate in the production of agrochemicals and pharmaceuticals. Its unique structure, featuring nitro and trifluoromethoxy groups, makes it valuable in developing herbicides and pesticides, where it enhances efficacy and selectivity. Additionally, it is employed in research settings to study chemical reactions involving electron-withdrawing groups, aiding in the design of novel materials and active ingredients. Its app

Used primarily in the synthesis of advanced organic compounds, it serves as a key intermediate in the production of agrochemicals and pharmaceuticals. Its unique structure, featuring nitro and trifluoromethoxy groups, makes it valuable in developing herbicides and pesticides, where it enhances efficacy and selectivity. Additionally, it is employed in research settings to study chemical reactions involving electron-withdrawing groups, aiding in the design of novel materials and active ingredients. Its application in medicinal chemistry includes the development of potential drug candidates targeting specific biological pathways.

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