4-(Difluoromethoxy)-3-methoxyaniline

≥95%

Reagent Code: #179456
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CAS Number 832739-34-1

science Other reagents with same CAS 832739-34-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.16 g/mol
Formula C₈H₉F₂NO₂
badge Registry Numbers
MDL Number MFCD04969123
inventory_2 Storage & Handling
Storage 2-8°C, avoiding light

description Product Description

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its ability to enhance bioavailability and metabolic stability in active ingredients. Its structure supports the development of compounds with improved selectivity and environmental persistence. Also employed in pharmaceutical research for building blocks in drug discovery, especially in molecules targeting central nervous system disorders. The difluoromethoxy and methoxy groups contribute to lipophilicity and electron-donating effects, making it valuable in optimizing pharmacokinetic properties.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿8,840.00
inventory 100mg
10-20 days ฿13,260.00
inventory 250mg
10-20 days ฿18,890.00
inventory 500mg
10-20 days ฿29,880.00
inventory 1g
10-20 days ฿40,320.00

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4-(Difluoromethoxy)-3-methoxyaniline
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Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its ability to enhance bioavailability and metabolic stability in active ingredients. Its structure supports the development of compounds with improved selectivity and environmental persistence. Also employed in pharmaceutical research for building blocks in drug discovery, especially in molecules targeting central nervous system disorders. The difluoromethoxy and methoxy groups contribute to li

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its ability to enhance bioavailability and metabolic stability in active ingredients. Its structure supports the development of compounds with improved selectivity and environmental persistence. Also employed in pharmaceutical research for building blocks in drug discovery, especially in molecules targeting central nervous system disorders. The difluoromethoxy and methoxy groups contribute to lipophilicity and electron-donating effects, making it valuable in optimizing pharmacokinetic properties.

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