2’-Fluoro-5’-(trifluoromethyl)acetophenone

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Reagent Code: #172481
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CAS Number 202664-53-7

science Other reagents with same CAS 202664-53-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.14 g/mol
Formula C₉H₆F₄O
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MDL Number MFCD00061248
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of antifungal and anti-inflammatory agents. Its fluorinated structure enhances metabolic stability and bioavailability in drug candidates. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where trifluoromethyl and fluoro substituents improve binding affinity and resistance to oxidative degradation. Also utilized in agrochemicals for creating herbicides and pesticides with increased efficacy and environmental persistence. Suitable for use in nucleophilic substitution and cross-coupling reactions due to its reactive ketone and fluorine groups.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,290.00
inventory 5g
10-20 days ฿2,990.00

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2’-Fluoro-5’-(trifluoromethyl)acetophenone
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Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of antifungal and anti-inflammatory agents. Its fluorinated structure enhances metabolic stability and bioavailability in drug candidates. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where trifluoromethyl and fluoro substituents improve binding affinity and resistance to oxidative degradation. Also utilized in agrochemicals for creating herbicides and pesticides wi
Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of antifungal and anti-inflammatory agents. Its fluorinated structure enhances metabolic stability and bioavailability in drug candidates. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where trifluoromethyl and fluoro substituents improve binding affinity and resistance to oxidative degradation. Also utilized in agrochemicals for creating herbicides and pesticides with increased efficacy and environmental persistence. Suitable for use in nucleophilic substitution and cross-coupling reactions due to its reactive ketone and fluorine groups.
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