bistrifluoromethanesulfonimidate

99.9%

Reagent Code: #143761
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Alias Lithium bistrifluoromethanesulfonimide
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CAS Number 90076-65-6

science Other reagents with same CAS 90076-65-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 287.09 g/mol
Formula C₂F₆LiNO₄S₂
badge Registry Numbers
EC Number 415-300-0
MDL Number MFCD00210017
thermostat Physical Properties
Melting Point 234-238 °C(lit.)
inventory_2 Storage & Handling
Density 1.334 g/cm3
Storage Room temperature, dry

description Product Description

Used as a versatile reagent in organic synthesis, particularly in trifluoromethylation and imidation reactions. It serves as a source of the trifluoromethanesulfonyl (triflyl) group, enabling the introduction of electron-withdrawing moieties to modify the stability and reactivity of organic compounds. Commonly applied in the preparation of sulfonamides and in catalytic transformations involving transition metals. Its strong electrophilic character makes it useful for generating reactive intermediates in fluorinated compound synthesis. Also employed in the development of pharmaceuticals and agrochemicals where fluorine-containing groups enhance metabolic stability and bioavailability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿480.00
inventory 5g
10-20 days ฿1,400.00
inventory 25g
10-20 days ฿4,400.00
inventory 100g
10-20 days ฿9,160.00
inventory 500g
10-20 days ฿25,600.00
inventory 2.5kg
10-20 days ฿82,000.00

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bistrifluoromethanesulfonimidate
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Used as a versatile reagent in organic synthesis, particularly in trifluoromethylation and imidation reactions. It serves as a source of the trifluoromethanesulfonyl (triflyl) group, enabling the introduction of electron-withdrawing moieties to modify the stability and reactivity of organic compounds. Commonly applied in the preparation of sulfonamides and in catalytic transformations involving transition metals. Its strong electrophilic character makes it useful for generating reactive intermediates in

Used as a versatile reagent in organic synthesis, particularly in trifluoromethylation and imidation reactions. It serves as a source of the trifluoromethanesulfonyl (triflyl) group, enabling the introduction of electron-withdrawing moieties to modify the stability and reactivity of organic compounds. Commonly applied in the preparation of sulfonamides and in catalytic transformations involving transition metals. Its strong electrophilic character makes it useful for generating reactive intermediates in fluorinated compound synthesis. Also employed in the development of pharmaceuticals and agrochemicals where fluorine-containing groups enhance metabolic stability and bioavailability.

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