Magnesium trifluoromethanesulfonate

98%

Reagent Code: #204724
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Alias Magnesium triflate
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CAS Number 60871-83-2

science Other reagents with same CAS 60871-83-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 322.44 g/mol
Formula (CF₃SO₃)₂Mg
badge Registry Numbers
MDL Number MFCD00042601
thermostat Physical Properties
Melting Point ≥300 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C, dry

description Product Description

Used as a Lewis acid catalyst in organic synthesis, particularly in Friedel-Crafts acylations and alkylations, enabling efficient carbon-carbon bond formation. Effective in promoting glycosylation reactions for carbohydrate chemistry due to its moisture tolerance and stability. Employed in coupling reactions such as Diels-Alder and Michael additions, offering high yields and selectivity. Also utilized in electrochemical applications and as a catalyst in esterification and transesterification processes for biodiesel production. Its non-corrosive nature and reusability make it suitable for green chemistry applications.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿320.00
inventory 25g
10-20 days ฿890.00
inventory 100g
10-20 days ฿3,400.00
inventory 500g
10-20 days ฿16,020.00
inventory 2.5kg
10-20 days ฿80,000.00

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Magnesium trifluoromethanesulfonate
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Used as a Lewis acid catalyst in organic synthesis, particularly in Friedel-Crafts acylations and alkylations, enabling efficient carbon-carbon bond formation. Effective in promoting glycosylation reactions for carbohydrate chemistry due to its moisture tolerance and stability. Employed in coupling reactions such as Diels-Alder and Michael additions, offering high yields and selectivity. Also utilized in electrochemical applications and as a catalyst in esterification and transesterification processes fo

Used as a Lewis acid catalyst in organic synthesis, particularly in Friedel-Crafts acylations and alkylations, enabling efficient carbon-carbon bond formation. Effective in promoting glycosylation reactions for carbohydrate chemistry due to its moisture tolerance and stability. Employed in coupling reactions such as Diels-Alder and Michael additions, offering high yields and selectivity. Also utilized in electrochemical applications and as a catalyst in esterification and transesterification processes for biodiesel production. Its non-corrosive nature and reusability make it suitable for green chemistry applications.

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