3-(2,2,2-trifluoroacetyl)benzoic acid

≥95%

Reagent Code: #240215
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CAS Number 213598-05-1

science Other reagents with same CAS 213598-05-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.13 g/mol
Formula C₉H₅F₃O₃
badge Registry Numbers
MDL Number MFCD13173376
thermostat Physical Properties
Melting Point 94-95 °C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and central nervous system agents. Its trifluoromethyl ketone functionality allows for selective transformations in medicinal chemistry, enhancing metabolic stability and bioavailability in drug candidates. Also employed in the preparation of fluorinated organic compounds where the trifluoromethyl group imparts favorable electronic and lipophilic properties. Commonly utilized in research settings for designing enzyme inhibitors due to the electrophilic nature of the carbonyl group adjacent to the trifluoromethyl moiety.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,790.00
inventory 250mg
10-20 days ฿4,360.00
inventory 5g
10-20 days ฿35,520.00
inventory 10g
10-20 days ฿61,750.00
inventory 1g
10-20 days ฿11,190.00
3-(2,2,2-trifluoroacetyl)benzoic acid
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and central nervous system agents. Its trifluoromethyl ketone functionality allows for selective transformations in medicinal chemistry, enhancing metabolic stability and bioavailability in drug candidates. Also employed in the preparation of fluorinated organic compounds where the trifluoromethyl group imparts favorable electronic and lipophilic properties. Commonly utilized in research sett

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and central nervous system agents. Its trifluoromethyl ketone functionality allows for selective transformations in medicinal chemistry, enhancing metabolic stability and bioavailability in drug candidates. Also employed in the preparation of fluorinated organic compounds where the trifluoromethyl group imparts favorable electronic and lipophilic properties. Commonly utilized in research settings for designing enzyme inhibitors due to the electrophilic nature of the carbonyl group adjacent to the trifluoromethyl moiety.

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