ethyl (E)-3-(4-(trifluoromethoxy)phenyl)acrylate

98%

Reagent Code: #183788
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CAS Number 866207-69-4

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 260.21 g/mol
Formula C₁₂H₁₁F₃O₃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of biologically active compounds. Its α,β-unsaturated ester structure makes it valuable in Michael addition reactions and other carbon-carbon bond-forming processes. Commonly employed in medicinal chemistry for constructing fluorinated analogs of natural products and drug candidates, where the trifluoromethoxy group enhances metabolic stability and lipophilicity. Also utilized in the preparation of liquid crystal materials and functional polymers due to its rigid aromatic core and polar substituent.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿6,480.00
inventory 5g
10-20 days ฿16,020.00
inventory 25g
10-20 days ฿55,800.00
inventory 250mg
10-20 days ฿2,210.00
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ethyl (E)-3-(4-(trifluoromethoxy)phenyl)acrylate
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of biologically active compounds. Its α,β-unsaturated ester structure makes it valuable in Michael addition reactions and other carbon-carbon bond-forming processes. Commonly employed in medicinal chemistry for constructing fluorinated analogs of natural products and drug candidates, where the trifluoromethoxy group enhances metabolic stability and lipophilicity. Also utilized in the preparat

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of biologically active compounds. Its α,β-unsaturated ester structure makes it valuable in Michael addition reactions and other carbon-carbon bond-forming processes. Commonly employed in medicinal chemistry for constructing fluorinated analogs of natural products and drug candidates, where the trifluoromethoxy group enhances metabolic stability and lipophilicity. Also utilized in the preparation of liquid crystal materials and functional polymers due to its rigid aromatic core and polar substituent.

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