Bis(methylthio)(trimethylsilyl)methane

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Reagent Code: #147673
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CAS Number 37891-79-5

science Other reagents with same CAS 37891-79-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.4 g/mol
Formula C₆H₁₆S₂Si
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MDL Number MFCD01631301
inventory_2 Storage & Handling
Storage Room temperature, stored in inert gas

description Product Description

Used as a versatile reagent in organic synthesis, particularly for the introduction of methylthio groups into molecules. It serves as a sulfur transfer agent in the preparation of sulfides and disulfides, which are important in pharmaceuticals and agrochemicals. Its trimethylsilyl group enhances reactivity and solubility in nonpolar solvents, making it effective in mild reaction conditions. Commonly employed in the synthesis of biologically active compounds where controlled sulfur incorporation is required. Also utilized in the development of specialty materials, including ligands for catalysis and precursors for sulfur-containing polymers.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿885.50
inventory 1g
10-20 days ฿4,860.00

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Bis(methylthio)(trimethylsilyl)methane
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Used as a versatile reagent in organic synthesis, particularly for the introduction of methylthio groups into molecules. It serves as a sulfur transfer agent in the preparation of sulfides and disulfides, which are important in pharmaceuticals and agrochemicals. Its trimethylsilyl group enhances reactivity and solubility in nonpolar solvents, making it effective in mild reaction conditions. Commonly employed in the synthesis of biologically active compounds where controlled sulfur incorporation is requir

Used as a versatile reagent in organic synthesis, particularly for the introduction of methylthio groups into molecules. It serves as a sulfur transfer agent in the preparation of sulfides and disulfides, which are important in pharmaceuticals and agrochemicals. Its trimethylsilyl group enhances reactivity and solubility in nonpolar solvents, making it effective in mild reaction conditions. Commonly employed in the synthesis of biologically active compounds where controlled sulfur incorporation is required. Also utilized in the development of specialty materials, including ligands for catalysis and precursors for sulfur-containing polymers.

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