2,2,2-Trifluoro-1-(o-tolyl)ethan-1-one

≥95%

Reagent Code: #244387
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CAS Number 341-39-9

science Other reagents with same CAS 341-39-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 188.15 g/mol
Formula C₉H₇F₃O
badge Registry Numbers
MDL Number MFCD01319968
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated organic compounds. Its trifluoromethyl ketone group enables unique reactivity in condensation and nucleophilic addition reactions, making it valuable in building complex molecules. Commonly employed in the preparation of bioactive agents where fluorine substitution enhances metabolic stability and lipophilicity. Also utilized in research settings for the design of novel synthetic pathways involving aromatic ketones with electron-withdrawing groups.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,050.00
inventory 10g
10-20 days ฿86,440.00
inventory 100mg
10-20 days ฿4,440.00
inventory 5g
10-20 days ฿46,160.00
inventory 1g
10-20 days ฿14,090.00
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2,2,2-Trifluoro-1-(o-tolyl)ethan-1-one
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated organic compounds. Its trifluoromethyl ketone group enables unique reactivity in condensation and nucleophilic addition reactions, making it valuable in building complex molecules. Commonly employed in the preparation of bioactive agents where fluorine substitution enhances metabolic stability and lipophilicity. Also utilized in research settings for the design of novel synthet

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated organic compounds. Its trifluoromethyl ketone group enables unique reactivity in condensation and nucleophilic addition reactions, making it valuable in building complex molecules. Commonly employed in the preparation of bioactive agents where fluorine substitution enhances metabolic stability and lipophilicity. Also utilized in research settings for the design of novel synthetic pathways involving aromatic ketones with electron-withdrawing groups.

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