(E)-Methyl 3-(2-(trifluoromethyl)phenyl)acrylate

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Reagent Code: #181159
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CAS Number 157518-53-1

science Other reagents with same CAS 157518-53-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.18 g/mol
Formula C₁₁H₉F₃O₂
badge Registry Numbers
MDL Number MFCD04973007
thermostat Physical Properties
Boiling Point 254.9±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.251±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antifungal, anti-inflammatory, or herbicidal properties. Its α,β-unsaturated ester structure makes it suitable for Michael addition reactions and other conjugate additions in organic synthesis. Commonly employed in medicinal chemistry for constructing trifluoromethyl-substituted aromatic compounds, which can enhance metabolic stability and lipophilicity in drug candidates. Also utilized in the preparation of liquid crystals and functional materials due to the electron-withdrawing nature of the trifluoromethyl group.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,380.00
inventory 25g
10-20 days ฿4,800.00
inventory 100g
10-20 days ฿15,840.00

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(E)-Methyl 3-(2-(trifluoromethyl)phenyl)acrylate
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antifungal, anti-inflammatory, or herbicidal properties. Its α,β-unsaturated ester structure makes it suitable for Michael addition reactions and other conjugate additions in organic synthesis. Commonly employed in medicinal chemistry for constructing trifluoromethyl-substituted aromatic compounds, which can enhance metabolic stability and lipophilicity in drug candid

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with antifungal, anti-inflammatory, or herbicidal properties. Its α,β-unsaturated ester structure makes it suitable for Michael addition reactions and other conjugate additions in organic synthesis. Commonly employed in medicinal chemistry for constructing trifluoromethyl-substituted aromatic compounds, which can enhance metabolic stability and lipophilicity in drug candidates. Also utilized in the preparation of liquid crystals and functional materials due to the electron-withdrawing nature of the trifluoromethyl group.

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