(E)-3-(4,4,4-Trifluoro-3-oxobut-1-en-1-yl)benzonitrile

95%

Reagent Code: #81006
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CAS Number 101048-56-0

science Other reagents with same CAS 101048-56-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.17 g/mol
Formula C₁₁H₆F₃NO
badge Registry Numbers
MDL Number MFCD16615234
thermostat Physical Properties
Boiling Point 260.2±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.30±0.1 g/cm3(Predicted)
Storage room temperature

description Product Description

This chemical is primarily used in the synthesis of advanced organic compounds, particularly in the development of pharmaceuticals and agrochemicals. Its unique structure, featuring a trifluoromethyl group and a nitrile moiety, makes it a valuable intermediate in creating molecules with potential biological activity. It is often employed in cross-coupling reactions and as a building block for designing inhibitors or modulators of specific enzymes or receptors. Additionally, its electron-withdrawing properties enhance its utility in the preparation of materials with specific electronic or optical characteristics, such as organic semiconductors or light-emitting diodes (LEDs). Its application extends to research and development in medicinal chemistry, where it contributes to the discovery of new therapeutic agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿31,500.00
inventory 250mg
10-20 days ฿45,000.00

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(E)-3-(4,4,4-Trifluoro-3-oxobut-1-en-1-yl)benzonitrile
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This chemical is primarily used in the synthesis of advanced organic compounds, particularly in the development of pharmaceuticals and agrochemicals. Its unique structure, featuring a trifluoromethyl group and a nitrile moiety, makes it a valuable intermediate in creating molecules with potential biological activity. It is often employed in cross-coupling reactions and as a building block for designing inhibitors or modulators of specific enzymes or receptors. Additionally, its electron-withdrawing prope

This chemical is primarily used in the synthesis of advanced organic compounds, particularly in the development of pharmaceuticals and agrochemicals. Its unique structure, featuring a trifluoromethyl group and a nitrile moiety, makes it a valuable intermediate in creating molecules with potential biological activity. It is often employed in cross-coupling reactions and as a building block for designing inhibitors or modulators of specific enzymes or receptors. Additionally, its electron-withdrawing properties enhance its utility in the preparation of materials with specific electronic or optical characteristics, such as organic semiconductors or light-emitting diodes (LEDs). Its application extends to research and development in medicinal chemistry, where it contributes to the discovery of new therapeutic agents.

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