Thulium(III) trifluoromethanesulfonate

98%

Reagent Code: #239638
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Alias Thrombomethanesulfonate
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CAS Number 141478-68-4

science Other reagents with same CAS 141478-68-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 616.14 g/mol
Formula C₃F₉O₉S₃Tm
badge Registry Numbers
MDL Number MFCD00209617
inventory_2 Storage & Handling
Density 1.7
Storage Room temperature

description Product Description

Widely used as a Lewis acid catalyst in organic synthesis, enabling efficient and selective transformations under mild conditions. Particularly effective in promoting carbon-carbon and carbon-heteroatom bond-forming reactions, including Friedel-Crafts alkylations, aldol condensations, and Michael additions. Exhibits high stability and reusability in aqueous and biphasic reaction systems, making it suitable for green chemistry applications. Its strong yet water-tolerant acidity allows catalysis in the presence of moisture, which is advantageous for one-pot reactions and industrial processes where anhydrous conditions are difficult to maintain. Also employed in luminescent materials and as a dopant in solid-state devices due to its unique optical properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿410.00
inventory 5g
10-20 days ฿1,990.00
inventory 25g
10-20 days ฿9,910.00
Thulium(III) trifluoromethanesulfonate
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Widely used as a Lewis acid catalyst in organic synthesis, enabling efficient and selective transformations under mild conditions. Particularly effective in promoting carbon-carbon and carbon-heteroatom bond-forming reactions, including Friedel-Crafts alkylations, aldol condensations, and Michael additions. Exhibits high stability and reusability in aqueous and biphasic reaction systems, making it suitable for green chemistry applications. Its strong yet water-tolerant acidity allows catalysis in the pre

Widely used as a Lewis acid catalyst in organic synthesis, enabling efficient and selective transformations under mild conditions. Particularly effective in promoting carbon-carbon and carbon-heteroatom bond-forming reactions, including Friedel-Crafts alkylations, aldol condensations, and Michael additions. Exhibits high stability and reusability in aqueous and biphasic reaction systems, making it suitable for green chemistry applications. Its strong yet water-tolerant acidity allows catalysis in the presence of moisture, which is advantageous for one-pot reactions and industrial processes where anhydrous conditions are difficult to maintain. Also employed in luminescent materials and as a dopant in solid-state devices due to its unique optical properties.

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