3-(Trifluoromethoxy)-Benzenepropanoic Acid

≥98%

Reagent Code: #241102
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CAS Number 168833-77-0

science Other reagents with same CAS 168833-77-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.17 g/mol
Formula C₁₀H₉F₃O₃
badge Registry Numbers
MDL Number MFCD01317834
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and central nervous system agents. Its trifluoromethoxy group enhances metabolic stability and lipophilicity, making it valuable in drug design for improving bioavailability and target binding. Also employed in agrochemicals for creating herbicides and pesticides due to the electron-withdrawing nature of the trifluoromethoxy moiety, which can increase compound persistence and activity. Commonly utilized in research settings for structure-activity relationship (SAR) studies involving carboxylic acid derivatives.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,650.00
inventory 5g
10-20 days ฿36,880.00
inventory 1g
10-20 days ฿9,220.00
3-(Trifluoromethoxy)-Benzenepropanoic Acid
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and central nervous system agents. Its trifluoromethoxy group enhances metabolic stability and lipophilicity, making it valuable in drug design for improving bioavailability and target binding. Also employed in agrochemicals for creating herbicides and pesticides due to the electron-withdrawing nature of the trifluoromethoxy moiety, which can increase compound persistence and activity. Common

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and central nervous system agents. Its trifluoromethoxy group enhances metabolic stability and lipophilicity, making it valuable in drug design for improving bioavailability and target binding. Also employed in agrochemicals for creating herbicides and pesticides due to the electron-withdrawing nature of the trifluoromethoxy moiety, which can increase compound persistence and activity. Commonly utilized in research settings for structure-activity relationship (SAR) studies involving carboxylic acid derivatives.

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