Trimethylsilyl chlorosulfonate

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Reagent Code: #242436
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CAS Number 4353-77-9

science Other reagents with same CAS 4353-77-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 188.71 g/mol
Formula ClSO₃Si(CH₃)₃
badge Registry Numbers
MDL Number MFCD00040471
thermostat Physical Properties
Melting Point −26 °C (lit.)
Boiling Point 168-169 °C (lit.)
inventory_2 Storage & Handling
Density 1.225 g/mL at 25 °C (lit.)
Storage 2~8 °C, sealed, dry, inert gas

description Product Description

Used as a powerful sulfonating and silylating reagent in organic synthesis. It efficiently introduces sulfonyl groups into aromatic and heteroaromatic compounds under mild conditions. Commonly applied in the preparation of sulfonate esters, which serve as intermediates in pharmaceuticals and agrochemicals. Also useful for the protection of hydroxyl groups via silylation, enabling selective transformations in complex molecule synthesis. Its high reactivity allows for fast reactions at low temperatures, improving yield and reducing side products. Handles moisture-sensitive reactions effectively when used in anhydrous environments.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿4,100.00
inventory 25g
10-20 days ฿14,880.00
inventory 1g
10-20 days ฿1,200.00

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Trimethylsilyl chlorosulfonate
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Used as a powerful sulfonating and silylating reagent in organic synthesis. It efficiently introduces sulfonyl groups into aromatic and heteroaromatic compounds under mild conditions. Commonly applied in the preparation of sulfonate esters, which serve as intermediates in pharmaceuticals and agrochemicals. Also useful for the protection of hydroxyl groups via silylation, enabling selective transformations in complex molecule synthesis. Its high reactivity allows for fast reactions at low temperatures, im

Used as a powerful sulfonating and silylating reagent in organic synthesis. It efficiently introduces sulfonyl groups into aromatic and heteroaromatic compounds under mild conditions. Commonly applied in the preparation of sulfonate esters, which serve as intermediates in pharmaceuticals and agrochemicals. Also useful for the protection of hydroxyl groups via silylation, enabling selective transformations in complex molecule synthesis. Its high reactivity allows for fast reactions at low temperatures, improving yield and reducing side products. Handles moisture-sensitive reactions effectively when used in anhydrous environments.

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