Methyl 4-(trifluoromethyl)benzoate

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Reagent Code: #205201
label
Alias Methyl 4-(trifluoromethyl)benzoate Methyl para-trifluoromethylbenzoate
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CAS Number 2967-66-0

science Other reagents with same CAS 2967-66-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.15 g/mol
Formula C₉H₇F₃O₂
badge Registry Numbers
MDL Number MFCD00042324
thermostat Physical Properties
Melting Point 13-14 °C(lit.)
Boiling Point 94-95 °C21 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.268 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds with enhanced metabolic stability and lipophilicity due to the presence of the trifluoromethyl group. Commonly employed in medicinal chemistry for the preparation of bioactive molecules, including anti-inflammatory and central nervous system agents. Also utilized in the design of fluorinated analogs in structure-activity relationship (SAR) studies to improve potency and selectivity. Its ester functionality allows for easy transformation into carboxylic acids, amides, or alcohols, making it a versatile building block in organic synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿270.00
inventory 25g
10-20 days ฿410.00
inventory 100g
10-20 days ฿1,450.00
inventory 500g
10-20 days ฿6,800.00
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Methyl 4-(trifluoromethyl)benzoate
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds with enhanced metabolic stability and lipophilicity due to the presence of the trifluoromethyl group. Commonly employed in medicinal chemistry for the preparation of bioactive molecules, including anti-inflammatory and central nervous system agents. Also utilized in the design of fluorinated analogs in structure-activity relationship (SAR) studies to improve potency and selectivity. Its ester functionality allows for easy transformation into carboxylic acids, amides, or alcohols, making it a versatile building block in organic synthesis.
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