4-(Trifluoromethylsulfonyl)benzonitrile

≥97%

Reagent Code: #244737
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CAS Number 312-21-0

science Other reagents with same CAS 312-21-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 235.18 g/mol
Formula C₈H₄F₃NO₂S
badge Registry Numbers
MDL Number MFCD01631631
thermostat Physical Properties
Melting Point 87-92 °C
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals due to the presence of both nitrile and trifluoromethylsulfonyl functional groups, which are key in forming biologically active molecules. The compound is particularly valuable in cross-coupling reactions, such as Suzuki and Heck reactions, where the trifluoromethylsulfonyl group acts as a good leaving group, enabling the formation of carbon-carbon bonds. It is also employed in the preparation of liquid crystals and organic electronic materials, where its electron-withdrawing properties help modulate the electronic characteristics of the final product. Its stability and reactivity profile make it suitable for use in mild reaction conditions, enhancing its utility in complex multi-step syntheses.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,900.00
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4-(Trifluoromethylsulfonyl)benzonitrile
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals due to the presence of both nitrile and trifluoromethylsulfonyl functional groups, which are key in forming biologically active molecules. The compound is particularly valuable in cross-coupling reactions, such as Suzuki and Heck reactions, where the trifluoromethylsulfonyl group acts as a good leaving group, enabling the formation of carbon-carbon bonds. It is also employed in the preparation of liquid crystals and organic ele

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals due to the presence of both nitrile and trifluoromethylsulfonyl functional groups, which are key in forming biologically active molecules. The compound is particularly valuable in cross-coupling reactions, such as Suzuki and Heck reactions, where the trifluoromethylsulfonyl group acts as a good leaving group, enabling the formation of carbon-carbon bonds. It is also employed in the preparation of liquid crystals and organic electronic materials, where its electron-withdrawing properties help modulate the electronic characteristics of the final product. Its stability and reactivity profile make it suitable for use in mild reaction conditions, enhancing its utility in complex multi-step syntheses.

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