1-(Trifluoromethanesulfonyl)imidazole

≥98%

Reagent Code: #114492
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CAS Number 29540-81-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.14 g/mol
Formula C₄H₃F₃N₂O₂S
badge Registry Numbers
MDL Number MFCD00037891
thermostat Physical Properties
Boiling Point 40°C/10mmHg(lit.)
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is widely used as a reagent in organic synthesis, particularly for introducing the trifluoromethanesulfonyl group into molecules, which is valuable in creating compounds with enhanced stability and reactivity. It is commonly employed in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals, where the triflyl group acts as a strong electron-withdrawing moiety. Additionally, it serves as a key intermediate in the synthesis of complex organic molecules, including heterocycles and biologically active compounds. Its ability to act as a triflating agent makes it useful in cross-coupling reactions, enabling the formation of carbon-carbon and carbon-heteroatom bonds in advanced chemical processes.

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Test Parameter Specification
Appearance Colorless to almost colorless clear liquid
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,340.00
inventory 200mg
10-20 days ฿612.00
1-(Trifluoromethanesulfonyl)imidazole
This chemical is widely used as a reagent in organic synthesis, particularly for introducing the trifluoromethanesulfonyl group into molecules, which is valuable in creating compounds with enhanced stability and reactivity. It is commonly employed in the preparation of pharmaceuticals, agrochemicals, and specialty chemicals, where the triflyl group acts as a strong electron-withdrawing moiety. Additionally, it serves as a key intermediate in the synthesis of complex organic molecules, including heterocycles and biologically active compounds. Its ability to act as a triflating agent makes it useful in cross-coupling reactions, enabling the formation of carbon-carbon and carbon-heteroatom bonds in advanced chemical processes.
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