Dimethyl(methylthio)sulfonium Tetrafluoroborate

≥97%

Reagent Code: #122083
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CAS Number 5799-67-7

science Other reagents with same CAS 5799-67-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 196.03 g/mol
Formula C₃H₉BF₄S₂
badge Registry Numbers
MDL Number MFCD00011806
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Widely used as a methylating agent in organic synthesis, particularly for transferring methyl groups to nucleophiles such as alcohols, thiols, and amines. It is effective in the preparation of methylated derivatives of various compounds, including pharmaceuticals and agrochemicals. The chemical is also employed in the synthesis of sulfur-containing organic molecules, where it acts as a key reagent for introducing methylthio groups. Its stability and reactivity under mild conditions make it a preferred choice in laboratory settings for selective methylation reactions. Additionally, it finds application in the modification of polymers and materials to enhance their properties.

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Test Parameter Specification
Appearance White to almost white powder to crystal
Purity (%) 96.5-100%
Infrared Spectrum Conforms To Structure
NMR Conforms To Structure

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿4,200.00
inventory 1g
10-20 days ฿14,610.00

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Dimethyl(methylthio)sulfonium Tetrafluoroborate
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Widely used as a methylating agent in organic synthesis, particularly for transferring methyl groups to nucleophiles such as alcohols, thiols, and amines. It is effective in the preparation of methylated derivatives of various compounds, including pharmaceuticals and agrochemicals. The chemical is also employed in the synthesis of sulfur-containing organic molecules, where it acts as a key reagent for introducing methylthio groups. Its stability and reactivity under mild conditions make it a preferred ch

Widely used as a methylating agent in organic synthesis, particularly for transferring methyl groups to nucleophiles such as alcohols, thiols, and amines. It is effective in the preparation of methylated derivatives of various compounds, including pharmaceuticals and agrochemicals. The chemical is also employed in the synthesis of sulfur-containing organic molecules, where it acts as a key reagent for introducing methylthio groups. Its stability and reactivity under mild conditions make it a preferred choice in laboratory settings for selective methylation reactions. Additionally, it finds application in the modification of polymers and materials to enhance their properties.

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