Dysprosium(III) trifluoromethanesulfonate

98%

Reagent Code: #169173
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Alias dysprosium trifluoromethanesulfonate
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CAS Number 139177-62-1

science Other reagents with same CAS 139177-62-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 609.71 g/mol
Formula C₃DyF₉O₉S₃
badge Registry Numbers
MDL Number MFCD00209583
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

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 acylations, Diels-Alder cycloadditions, and glycosidation reactions. Exhibits high stability and reusability in aqueous and protic environments, making it suitable for green chemistry applications. Also employed in luminescent materials and coordination polymers due to its strong coordination ability and unique electronic properties.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿350.00
inventory 5g
10-20 days ฿900.00
inventory 25g
10-20 days ฿3,470.00
inventory 100g
10-20 days ฿10,680.00
inventory 10g
10-20 days ฿1,680.00

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Dysprosium(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 acylations, Diels-Alder cycloadditions, and glycosidation reactions. Exhibits high stability and reusability in aqueous and protic environments, making it suitable for green chemistry applications. Also employed in luminescent materials and coordination pol

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 acylations, Diels-Alder cycloadditions, and glycosidation reactions. Exhibits high stability and reusability in aqueous and protic environments, making it suitable for green chemistry applications. Also employed in luminescent materials and coordination polymers due to its strong coordination ability and unique electronic properties.

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