Trimethylsulfonium bromide

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Reagent Code: #240366
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CAS Number 3084-53-5

science Other reagents with same CAS 3084-53-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 157.07 g/mol
Formula C₃H₉BrS
badge Registry Numbers
MDL Number MFCD00051367
thermostat Physical Properties
Melting Point 203°C
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used as a methylating agent in organic synthesis, particularly for transferring methyl groups to nucleophiles such as amines, thiols, and enolates. It is effective in the preparation of quaternary ammonium compounds and in the synthesis of sulfonium ylides, which are key intermediates in reactions like the Johnson–Corey–Chaykovsky reaction for forming epoxides and cyclopropanes. Its stability and solubility in polar solvents make it suitable for use in a variety of solution-phase reactions. Also employed in the modification of biomolecules and in some pharmaceutical syntheses where controlled methylation is required.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿162.00
inventory 25g
10-20 days ฿290.00
inventory 100g
10-20 days ฿560.00
inventory 500g
10-20 days ฿2,680.00
inventory 2.5kg
10-20 days ฿12,770.00

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Trimethylsulfonium bromide
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Used as a methylating agent in organic synthesis, particularly for transferring methyl groups to nucleophiles such as amines, thiols, and enolates. It is effective in the preparation of quaternary ammonium compounds and in the synthesis of sulfonium ylides, which are key intermediates in reactions like the Johnson–Corey–Chaykovsky reaction for forming epoxides and cyclopropanes. Its stability and solubility in polar solvents make it suitable for use in a variety of solution-phase reactions. Also employed

Used as a methylating agent in organic synthesis, particularly for transferring methyl groups to nucleophiles such as amines, thiols, and enolates. It is effective in the preparation of quaternary ammonium compounds and in the synthesis of sulfonium ylides, which are key intermediates in reactions like the Johnson–Corey–Chaykovsky reaction for forming epoxides and cyclopropanes. Its stability and solubility in polar solvents make it suitable for use in a variety of solution-phase reactions. Also employed in the modification of biomolecules and in some pharmaceutical syntheses where controlled methylation is required.

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