3-(Trifluoromethyl)phenylacetic acid

98%

Reagent Code: #239745
label
Alias 3-(trifluoromethyl)phenylacetic acid; m-trifluoromethylphenylacetic acid
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CAS Number 351-35-9

science Other reagents with same CAS 351-35-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.15 g/mol
Formula C₉H₇F₃O₂
badge Registry Numbers
EC Number 206-511-7
MDL Number MFCD00004339
thermostat Physical Properties
Melting Point 76-79 °C(lit.)
Boiling Point 238C/775Torr
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in the synthesis of pharmaceuticals, particularly as an intermediate in the production of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in drug design for improving pharmacokinetic properties. Also employed in the development of agrochemicals, including herbicides and fungicides, due to the electron-withdrawing nature of the CF3 group that can increase compound stability and activity. Serves as a building block in organic synthesis for constructing complex molecules in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿600.00
inventory 100g
10-20 days ฿8,300.00
inventory 25g
10-20 days ฿2,330.00
inventory 500g
10-20 days ฿26,300.00

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3-(Trifluoromethyl)phenylacetic acid
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Used in the synthesis of pharmaceuticals, particularly as an intermediate in the production of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in drug design for improving pharmacokinetic properties. Also employed in the development of agrochemicals, including herbicides and fungicides, due to the electron-withdrawing nature of the CF3 group that can increase compound stability and a

Used in the synthesis of pharmaceuticals, particularly as an intermediate in the production of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in drug design for improving pharmacokinetic properties. Also employed in the development of agrochemicals, including herbicides and fungicides, due to the electron-withdrawing nature of the CF3 group that can increase compound stability and activity. Serves as a building block in organic synthesis for constructing complex molecules in medicinal chemistry research.

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