Ytterbium(III) Trifluoromethanesulfonate

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Reagent Code: #246198
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Alias phenylatrifluoromethanesulfonate
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CAS Number 54761-04-5

science Other reagents with same CAS 54761-04-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 620.25 g/mol
Formula C₃F₉O₉S₃Yb
badge Registry Numbers
MDL Number MFCD06200261
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Widely used as a Lewis acid catalyst in organic synthesis, enabling a variety of transformations under mild conditions. It is particularly effective in promoting carbon-carbon and carbon-heteroatom bond formations. Common applications include Friedel-Crafts acylations, Diels-Alder reactions, and Mukaiyama aldol reactions, where it offers high yields and selectivity. Its water tolerance makes it suitable for reactions in aqueous or moist environments, unlike many traditional Lewis acids. Also employed in the activation of carbonyl compounds and in polymerization reactions. Due to its stability and reusability, it is favored in green chemistry initiatives and industrial processes where efficient and environmentally friendly catalysis is required.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿470.00
inventory 25g
10-20 days ฿1,900.00
inventory 100g
10-20 days ฿6,850.00
inventory 500g
10-20 days ฿24,980.00

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Ytterbium(III) Trifluoromethanesulfonate
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Widely used as a Lewis acid catalyst in organic synthesis, enabling a variety of transformations under mild conditions. It is particularly effective in promoting carbon-carbon and carbon-heteroatom bond formations. Common applications include Friedel-Crafts acylations, Diels-Alder reactions, and Mukaiyama aldol reactions, where it offers high yields and selectivity. Its water tolerance makes it suitable for reactions in aqueous or moist environments, unlike many traditional Lewis acids. Also employed in the activation of carbonyl compounds and in polymerization reactions. Due to its stability and reusability, it is favored in green chemistry initiatives and industrial processes where efficient and environmentally friendly catalysis is required.
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