3-Nitro-6-(trifluoromethyl)pyridin-2(1H)-one

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Reagent Code: #219184
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CAS Number 117519-07-0

science Other reagents with same CAS 117519-07-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 208.09 g/mol
Formula C₆H₃F₃N₂O₃
badge Registry Numbers
MDL Number MFCD10696218
thermostat Physical Properties
Boiling Point 278.6±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.61±0.1 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive compounds. Its structure supports the creation of nitrogen-containing heterocycles, which are common in herbicides and insecticides. The electron-withdrawing nitro and trifluoromethyl groups enhance reactivity, making it valuable in cross-coupling reactions and nucleophilic substitutions during active ingredient formulation. Also explored in medicinal chemistry for potential neuroactive or anti-inflammatory agents due to its ability to interact with biological targets.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿490.00
inventory 1g
10-20 days ฿1,350.00
inventory 5g
10-20 days ฿5,700.00
3-Nitro-6-(trifluoromethyl)pyridin-2(1H)-one
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive compounds. Its structure supports the creation of nitrogen-containing heterocycles, which are common in herbicides and insecticides. The electron-withdrawing nitro and trifluoromethyl groups enhance reactivity, making it valuable in cross-coupling reactions and nucleophilic substitutions during active ingredient formulation. Also explored in medicinal chemistry for potential neuroac

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of agrochemicals and bioactive compounds. Its structure supports the creation of nitrogen-containing heterocycles, which are common in herbicides and insecticides. The electron-withdrawing nitro and trifluoromethyl groups enhance reactivity, making it valuable in cross-coupling reactions and nucleophilic substitutions during active ingredient formulation. Also explored in medicinal chemistry for potential neuroactive or anti-inflammatory agents due to its ability to interact with biological targets.

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