3-(Trifluoromethoxy)benzoic acid

98%

Reagent Code: #239682
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Alias 3-(trifluoromethoxy)benzoic acid; m-trifluoromethoxybenzoic acid
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CAS Number 1014-81-9

science Other reagents with same CAS 1014-81-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.12 g/mol
Formula C₈H₅F₃O₃
badge Registry Numbers
EC Number 213-802-2
MDL Number MFCD00041501
thermostat Physical Properties
Melting Point 89-92 °C(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key 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. Also employed in agrochemicals for creating herbicides and fungicides due to its ability to improve bioavailability and environmental persistence. Commonly utilized in research for modifying organic molecules to study structure-activity relationships.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿180.00
inventory 5g
10-20 days ฿520.00

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3-(Trifluoromethoxy)benzoic acid
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Used as a key 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. Also employed in agrochemicals for creating herbicides and fungicides due to its ability to improve bioavailability and environmental persistence. Commonly utilized in research for modifying organic molecules to study structure-activity relationsh

Used as a key 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. Also employed in agrochemicals for creating herbicides and fungicides due to its ability to improve bioavailability and environmental persistence. Commonly utilized in research for modifying organic molecules to study structure-activity relationships.

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