3-(Trifluoromethyl)Benzophenone

≥98%

Reagent Code: #241137
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CAS Number 728-81-4

science Other reagents with same CAS 728-81-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.22 g/mol
Formula C₁₄H₉F₃O
badge Registry Numbers
MDL Number MFCD00000389
thermostat Physical Properties
Melting Point 52-53 °C
inventory_2 Storage & Handling
Density 1.244g/mL
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in antimalarial and antifungal agents. Its structure supports the development of bioactive molecules due to the electron-withdrawing trifluoromethyl group enhancing metabolic stability. Also employed in agrochemicals for crop protection products, where it contributes to improved efficacy and environmental persistence. Additionally, serves as a building block in organic synthesis for fluorescent dyes and functional materials, benefiting from its rigid aromatic framework and halogenated substituent.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿2,540.00
inventory 25g
10-20 days ฿4,735.50
3-(Trifluoromethyl)Benzophenone
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in antimalarial and antifungal agents. Its structure supports the development of bioactive molecules due to the electron-withdrawing trifluoromethyl group enhancing metabolic stability. Also employed in agrochemicals for crop protection products, where it contributes to improved efficacy and environmental persistence. Additionally, serves as a building block in organic synthesis for fluorescent dyes and functional materials, ben

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in antimalarial and antifungal agents. Its structure supports the development of bioactive molecules due to the electron-withdrawing trifluoromethyl group enhancing metabolic stability. Also employed in agrochemicals for crop protection products, where it contributes to improved efficacy and environmental persistence. Additionally, serves as a building block in organic synthesis for fluorescent dyes and functional materials, benefiting from its rigid aromatic framework and halogenated substituent.

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