4-(Trifluoromethyl)benzoic acid

98%

Reagent Code: #239849
label
Alias p-trifluoromethylbenzoic acid
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CAS Number 455-24-3

science Other reagents with same CAS 455-24-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.12 g/mol
Formula C₈H₅F₃O₂
badge Registry Numbers
EC Number 207-242-8
MDL Number MFCD00002562
thermostat Physical Properties
Melting Point 219-220 °C(lit.)
Boiling Point 247°C 753mm
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in the synthesis of pharmaceuticals and agrochemicals due to the electron-withdrawing nature of the trifluoromethyl group, enhancing metabolic stability and bioavailability. Commonly employed as a building block in drug discovery, particularly in the development of anti-inflammatory, antifungal, and anticancer agents. Also utilized in materials science for designing liquid crystals and organic electronic materials where polarity and thermal stability are important. Its carboxylic acid functionality allows for easy derivatization into esters, amides, and other functional groups for targeted applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿270.00
inventory 25g
10-20 days ฿330.00
inventory 100g
10-20 days ฿1,170.00
inventory 500g
10-20 days ฿4,930.00
inventory 2.5kg
10-20 days ฿24,100.00
4-(Trifluoromethyl)benzoic acid
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Used in the synthesis of pharmaceuticals and agrochemicals due to the electron-withdrawing nature of the trifluoromethyl group, enhancing metabolic stability and bioavailability. Commonly employed as a building block in drug discovery, particularly in the development of anti-inflammatory, antifungal, and anticancer agents. Also utilized in materials science for designing liquid crystals and organic electronic materials where polarity and thermal stability are important. Its carboxylic acid functionality

Used in the synthesis of pharmaceuticals and agrochemicals due to the electron-withdrawing nature of the trifluoromethyl group, enhancing metabolic stability and bioavailability. Commonly employed as a building block in drug discovery, particularly in the development of anti-inflammatory, antifungal, and anticancer agents. Also utilized in materials science for designing liquid crystals and organic electronic materials where polarity and thermal stability are important. Its carboxylic acid functionality allows for easy derivatization into esters, amides, and other functional groups for targeted applications.

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