trifluoromethanesulfonylpyridinium salt

97%

Reagent Code: #238865
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CAS Number 2823408-48-4

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 444.36 g/mol
Formula C₁₂H₁₄O₅F₆N₂S₂
inventory_2 Storage & Handling
Storage -20 °C, Sealed, Dry

description Product Description

Widely used in organic synthesis as a highly effective trifluoromethanesulfonyl (triflyl) transfer reagent. It enables the introduction of the triflyl group into nucleophiles, which is valuable for creating sulfonate esters and amides—key intermediates in pharmaceuticals and agrochemicals. Particularly useful in the preparation of triflates from alcohols, enabling subsequent cross-coupling reactions. Its pyridinium structure enhances stability and reactivity under mild conditions, making it suitable for sensitive substrates. Employed in the synthesis of functional materials and active ingredients where strong electrophilic character and good leaving group ability are required.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,800.00
inventory 1g
10-20 days ฿13,000.00
inventory 5g
10-20 days ฿43,200.00
inventory 250mg
10-20 days ฿4,800.00
inventory 25g
10-20 days ฿156,200.00
trifluoromethanesulfonylpyridinium salt
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Widely used in organic synthesis as a highly effective trifluoromethanesulfonyl (triflyl) transfer reagent. It enables the introduction of the triflyl group into nucleophiles, which is valuable for creating sulfonate esters and amides—key intermediates in pharmaceuticals and agrochemicals. Particularly useful in the preparation of triflates from alcohols, enabling subsequent cross-coupling reactions. Its pyridinium structure enhances stability and reactivity under mild conditions, making it suitable for

Widely used in organic synthesis as a highly effective trifluoromethanesulfonyl (triflyl) transfer reagent. It enables the introduction of the triflyl group into nucleophiles, which is valuable for creating sulfonate esters and amides—key intermediates in pharmaceuticals and agrochemicals. Particularly useful in the preparation of triflates from alcohols, enabling subsequent cross-coupling reactions. Its pyridinium structure enhances stability and reactivity under mild conditions, making it suitable for sensitive substrates. Employed in the synthesis of functional materials and active ingredients where strong electrophilic character and good leaving group ability are required.

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