2-Nitro-5-(trifluoromethyl)phenylacetic acid

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Reagent Code: #219944
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CAS Number 927801-01-2

science Other reagents with same CAS 927801-01-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 249.1 g/mol
Formula C₉H₆F₃NO₄
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MDL Number MFCD08436986
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. Its structure allows for further functionalization, making it valuable in creating active pharmaceutical ingredients (APIs) with enhanced metabolic stability and bioavailability. Commonly employed in research settings for designing novel trifluoromethyl-containing compounds, which often exhibit improved pharmacokinetic properties. Also utilized in agrochemical research for developing new herbicides and pesticides due to the electron-withdrawing nature of the nitro and trifluoromethyl groups, which can enhance biological activity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,540.00
inventory 250mg
10-20 days ฿6,640.00

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2-Nitro-5-(trifluoromethyl)phenylacetic acid
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. Its structure allows for further functionalization, making it valuable in creating active pharmaceutical ingredients (APIs) with enhanced metabolic stability and bioavailability. Commonly employed in research settings for designing novel trifluoromethyl-containing compounds, which often exhibit improved pharmacokinetic properties. Also utilized in agrochemical research f

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. Its structure allows for further functionalization, making it valuable in creating active pharmaceutical ingredients (APIs) with enhanced metabolic stability and bioavailability. Commonly employed in research settings for designing novel trifluoromethyl-containing compounds, which often exhibit improved pharmacokinetic properties. Also utilized in agrochemical research for developing new herbicides and pesticides due to the electron-withdrawing nature of the nitro and trifluoromethyl groups, which can enhance biological activity.

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