3'-(Trifluoromethyl)acetophenone

97%

Reagent Code: #239786
label
Alias m-trifluoromethylacetophenone;-trifluoromethylacetophenone, 3-trifluoromethylacetophenone
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CAS Number 349-76-8

science Other reagents with same CAS 349-76-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 188.15 g/mol
Formula C₉H₇F₃O
badge Registry Numbers
EC Number 206-490-4
MDL Number MFCD00000391
thermostat Physical Properties
Boiling Point 198-200 °C(lit.)
inventory_2 Storage & Handling
Density 1.235 g/mL at 25 °C(lit.)
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 trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in drug design. Also employed in the preparation of agrochemicals and functional materials due to its electron-withdrawing properties and structural versatility. Commonly utilized in Friedel-Crafts acylation and nucleophilic addition reactions to build complex organic molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿400.00
inventory 25g
10-20 days ฿880.00
inventory 100g
10-20 days ฿3,220.00
inventory 1g
10-20 days ฿300.00
inventory 500g
10-20 days ฿16,000.00
3'-(Trifluoromethyl)acetophenone
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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 trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in drug design. Also employed in the preparation of agrochemicals and functional materials due to its electron-withdrawing properties and structural versatility. Commonly utilized in Friedel-Crafts acylation and nucleophilic addition reactions to build complex org

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and central nervous system agents. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in drug design. Also employed in the preparation of agrochemicals and functional materials due to its electron-withdrawing properties and structural versatility. Commonly utilized in Friedel-Crafts acylation and nucleophilic addition reactions to build complex organic molecules.

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