2-Amino-4-(trifluoromethyl)benzoic Acid

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Reagent Code: #135484
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CAS Number 402-13-1

science Other reagents with same CAS 402-13-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.14 g/mol
Formula C₈H₆F₃NO₂
badge Registry Numbers
MDL Number MFCD00519334
thermostat Physical Properties
Melting Point 175°C(lit.)
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to the presence of both amino and carboxylic acid functional groups along with the trifluoromethyl moiety. The electron-withdrawing trifluoromethyl group enhances metabolic stability and bioavailability in drug molecules, making this compound valuable in medicinal chemistry. It is commonly employed in the development of anti-inflammatory agents, kinase inhibitors, and central nervous system modulators. Additionally, it serves as a building block in the preparation of dyes, fluorescent probes, and specialty polymers where fluorine substitution improves thermal and oxidative stability.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿144.00
inventory 5g
10-20 days ฿860.00

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2-Amino-4-(trifluoromethyl)benzoic Acid
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Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to the presence of both amino and carboxylic acid functional groups along with the trifluoromethyl moiety. The electron-withdrawing trifluoromethyl group enhances metabolic stability and bioavailability in drug molecules, making this compound valuable in medicinal chemistry. It is commonly employed in the development of anti-inflammatory agents, kinase inhibitors, and central nervous system modulators. Additi

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to the presence of both amino and carboxylic acid functional groups along with the trifluoromethyl moiety. The electron-withdrawing trifluoromethyl group enhances metabolic stability and bioavailability in drug molecules, making this compound valuable in medicinal chemistry. It is commonly employed in the development of anti-inflammatory agents, kinase inhibitors, and central nervous system modulators. Additionally, it serves as a building block in the preparation of dyes, fluorescent probes, and specialty polymers where fluorine substitution improves thermal and oxidative stability.

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