4'-(Trifluoromethyl)acetophenone

98%

Reagent Code: #240051
label
Alias P-trichloromethylacetone
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CAS Number 709-63-7

science Other reagents with same CAS 709-63-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 188.15 g/mol
Formula CF₃C₆H₄COCH₃
badge Registry Numbers
EC Number 211-913-0
MDL Number MFCD00000401
thermostat Physical Properties
Melting Point 30-33 °C(lit.)
Boiling Point 79-80 °C8 mm Hg(lit.)
inventory_2 Storage & Handling
Density 0.92
Storage Room temperature, flammable area

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in antimalarial and anti-inflammatory drugs. Its electron-withdrawing trifluoromethyl group enhances metabolic stability and bioavailability in drug candidates. Commonly employed in the preparation of chalcone derivatives and other fluorinated organic compounds with biological activity. Also utilized in agrochemicals for developing herbicides and pesticides due to the improved lipophilicity and resistance to degradation provided by the CF3 group. Frequently applied in research settings for building blocks in medicinal chemistry and structure-activity relationship (SAR) studies.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿260.00
inventory 5g
10-20 days ฿300.00
inventory 25g
10-20 days ฿1,050.00
inventory 100g
10-20 days ฿4,010.00

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4'-(Trifluoromethyl)acetophenone
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in antimalarial and anti-inflammatory drugs. Its electron-withdrawing trifluoromethyl group enhances metabolic stability and bioavailability in drug candidates. Commonly employed in the preparation of chalcone derivatives and other fluorinated organic compounds with biological activity. Also utilized in agrochemicals for developing herbicides and pesticides due to the improved lipophilicity and resistance to degradation provided

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in antimalarial and anti-inflammatory drugs. Its electron-withdrawing trifluoromethyl group enhances metabolic stability and bioavailability in drug candidates. Commonly employed in the preparation of chalcone derivatives and other fluorinated organic compounds with biological activity. Also utilized in agrochemicals for developing herbicides and pesticides due to the improved lipophilicity and resistance to degradation provided by the CF3 group. Frequently applied in research settings for building blocks in medicinal chemistry and structure-activity relationship (SAR) studies.

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