trans-4-(Trifluoromethyl)cinnamic acid

97%

Reagent Code: #239609
label
Alias 4-Trifluoromethylcinnamic acid; p-Trifluoromethylcinnamic acid
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CAS Number 16642-92-5

science Other reagents with same CAS 16642-92-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.16 g/mol
Formula C₁₀H₇F₃O₂
badge Registry Numbers
MDL Number MFCD00002696
thermostat Physical Properties
Melting Point 231-233 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and anticancer agents. Its trifluoromethyl group enhances metabolic stability and bioavailability, making it valuable in medicinal chemistry. Also employed in the preparation of liquid crystals and organic semiconductors due to its rigid structure and electronic properties. Commonly utilized in research for designing new biologically active compounds and in agrochemicals for improved pesticidal activity. Additionally, applied in photochemical research owing to its photoisomerization properties, enabling uses in photoresponsive materials such as solar cells and optical devices.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿400.00
inventory 25g
10-20 days ฿1,390.00
inventory 100g
10-20 days ฿4,980.00
trans-4-(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 anticancer agents. Its trifluoromethyl group enhances metabolic stability and bioavailability, making it valuable in medicinal chemistry. Also employed in the preparation of liquid crystals and organic semiconductors due to its rigid structure and electronic properties. Commonly utilized in research for designing new biologically active compounds and in agrochemicals for improved pesti

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and anticancer agents. Its trifluoromethyl group enhances metabolic stability and bioavailability, making it valuable in medicinal chemistry. Also employed in the preparation of liquid crystals and organic semiconductors due to its rigid structure and electronic properties. Commonly utilized in research for designing new biologically active compounds and in agrochemicals for improved pesticidal activity. Additionally, applied in photochemical research owing to its photoisomerization properties, enabling uses in photoresponsive materials such as solar cells and optical devices.

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