Ethyl 3-(Trifluoromethyl)Benzoate

≥98%

Reagent Code: #182943
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CAS Number 76783-59-0

science Other reagents with same CAS 76783-59-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.17 g/mol
Formula C₁₀H₉F₃O₂
badge Registry Numbers
MDL Number MFCD00013560
thermostat Physical Properties
Boiling Point 100 °C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients for anti-inflammatory and central nervous system drugs. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in medicinal chemistry. Also employed in agrochemical research for designing novel pesticides and herbicides due to the electron-withdrawing properties that improve bioavailability and environmental persistence. Commonly utilized in organic synthesis as a building block for constructing complex fluorinated molecules.

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Size Availability Unit Price Quantity
inventory 100g
10-20 days ฿2,070.00
inventory 500g
10-20 days ฿10,320.00
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Ethyl 3-(Trifluoromethyl)Benzoate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients for anti-inflammatory and central nervous system drugs. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in medicinal chemistry. Also employed in agrochemical research for designing novel pesticides and herbicides due to the electron-withdrawing properties that improve bioavailability and environmental persistence. Commonly utilized in organic synt

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of active ingredients for anti-inflammatory and central nervous system drugs. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in medicinal chemistry. Also employed in agrochemical research for designing novel pesticides and herbicides due to the electron-withdrawing properties that improve bioavailability and environmental persistence. Commonly utilized in organic synthesis as a building block for constructing complex fluorinated molecules.

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