(E)-2-(Trifluoromethyl)cinnamic Acid

>98%(GC&T)

Reagent Code: #184082
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CAS Number 98386-81-3

science Other reagents with same CAS 98386-81-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.16 g/mol
Formula C₁₀H₇F₃O₂
badge Registry Numbers
MDL Number MFCD00004381
thermostat Physical Properties
Melting Point 204 °C
Boiling Point 276.9 °C at 760mmHg
inventory_2 Storage & Handling
Density 1.363 g/cm3
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and antimicrobial agents. Its α,β-unsaturated carbonyl structure with a trifluoromethyl group enhances reactivity in conjugate addition reactions, making it valuable in medicinal chemistry for building bioactive molecules. Also employed in the design of agrochemicals due to the metabolic stability imparted by the fluorinated moiety. Additionally, it serves as a building block in organic synthesis for creating fluorinated analogs of natural products and functional materials.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿800.00
inventory 10g
10-20 days ฿1,530.00
inventory 100g
10-20 days ฿11,740.00
inventory 500g
10-20 days ฿38,430.00
inventory 25g
10-20 days ฿3,450.00

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(E)-2-(Trifluoromethyl)cinnamic Acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and antimicrobial agents. Its α,β-unsaturated carbonyl structure with a trifluoromethyl group enhances reactivity in conjugate addition reactions, making it valuable in medicinal chemistry for building bioactive molecules. Also employed in the design of agrochemicals due to the metabolic stability imparted by the fluorinated moiety. Additionally, it serves as a building block in organic sy

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and antimicrobial agents. Its α,β-unsaturated carbonyl structure with a trifluoromethyl group enhances reactivity in conjugate addition reactions, making it valuable in medicinal chemistry for building bioactive molecules. Also employed in the design of agrochemicals due to the metabolic stability imparted by the fluorinated moiety. Additionally, it serves as a building block in organic synthesis for creating fluorinated analogs of natural products and functional materials.

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