4-(Trifluoromethyl)phenylacetic acid

98%

Reagent Code: #239888
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Alias 4-(trifluoromethyl)phenylacetic acid; 4-trifluoromethylphenylacetic acid, p-trifluoromethylphenylacetic acid
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CAS Number 32857-62-8

science Other reagents with same CAS 32857-62-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.15 g/mol
Formula C₉H₇F₃O₂
badge Registry Numbers
EC Number 251-263-5
MDL Number MFCD00004352
thermostat Physical Properties
Melting Point 82-85 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory agents, non-steroidal anti-inflammatory drugs (NSAIDs), central nervous system agents, anti-cancer drugs, and compounds targeting specific hormone receptors. Its trifluoromethyl group enhances metabolic stability, lipophilicity, solubility in fats, and molecular stability, making it valuable in drug design for improved efficacy, longer duration in the body, bioavailability, and binding affinity. Commonly employed as an intermediate in the preparation of active pharmaceutical ingredients (APIs) due to its easily modifiable structure for specific, high-potency derivatives. Also utilized in agrochemicals for the production of herbicides and fungicides, where the electron-withdrawing nature of the trifluoromethyl group enhances biological activity.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿720.00
inventory 25g
10-20 days ฿3,540.00
inventory 100g
10-20 days ฿13,880.00

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4-(Trifluoromethyl)phenylacetic acid
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Used in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory agents, non-steroidal anti-inflammatory drugs (NSAIDs), central nervous system agents, anti-cancer drugs, and compounds targeting specific hormone receptors. Its trifluoromethyl group enhances metabolic stability, lipophilicity, solubility in fats, and molecular stability, making it valuable in drug design for improved efficacy, longer duration in the body, bioavailability, and binding affinity. Commonly employ

Used in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory agents, non-steroidal anti-inflammatory drugs (NSAIDs), central nervous system agents, anti-cancer drugs, and compounds targeting specific hormone receptors. Its trifluoromethyl group enhances metabolic stability, lipophilicity, solubility in fats, and molecular stability, making it valuable in drug design for improved efficacy, longer duration in the body, bioavailability, and binding affinity. Commonly employed as an intermediate in the preparation of active pharmaceutical ingredients (APIs) due to its easily modifiable structure for specific, high-potency derivatives. Also utilized in agrochemicals for the production of herbicides and fungicides, where the electron-withdrawing nature of the trifluoromethyl group enhances biological activity.

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