3-Nitro-5-(trifluoromethyl)picolinonitrile

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Reagent Code: #214745
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CAS Number 866775-16-8

science Other reagents with same CAS 866775-16-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.1 g/mol
Formula C₇H₂F₃N₃O₂
badge Registry Numbers
MDL Number MFCD14702310
thermostat Physical Properties
Boiling Point 313.3±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.58±0.1 g/cm3(Predicted)
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 herbicides and fungicides due to its electron-withdrawing nitrile and trifluoromethyl groups enhancing bioactivity. Its structure supports the creation of complex heterocyclic compounds, making it valuable in medicinal chemistry for designing active ingredients with improved metabolic stability and target selectivity. Also employed in research for constructing nitrogen-rich scaffolds in crop protection agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,620.00
inventory 1g
10-20 days ฿30,340.00

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3-Nitro-5-(trifluoromethyl)picolinonitrile
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and fungicides due to its electron-withdrawing nitrile and trifluoromethyl groups enhancing bioactivity. Its structure supports the creation of complex heterocyclic compounds, making it valuable in medicinal chemistry for designing active ingredients with improved metabolic stability and target selectivity. Also employed in research for constructing nitrogen-rich scaffolds in cr

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and fungicides due to its electron-withdrawing nitrile and trifluoromethyl groups enhancing bioactivity. Its structure supports the creation of complex heterocyclic compounds, making it valuable in medicinal chemistry for designing active ingredients with improved metabolic stability and target selectivity. Also employed in research for constructing nitrogen-rich scaffolds in crop protection agents.

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