TRIMETHYLSILYLBENZENESULFONATE

97%

Reagent Code: #88325
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CAS Number 17882-06-3

science Other reagents with same CAS 17882-06-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.36 g/mol
Formula C₉H₁₄O₃SSi
thermostat Physical Properties
Melting Point 48 °F
Boiling Point 154-156 °C(lit.)
inventory_2 Storage & Handling
Density 1.138 g/mL at 25 °C(lit.)
Storage 2-8°C, sealed, dry

description Product Description

Trimethylsilylbenzenesulfonate is primarily used as a reagent in organic synthesis, particularly in the protection of hydroxyl groups. It acts as a silylating agent, converting alcohols into their corresponding trimethylsilyl ethers, which are more stable and less reactive under certain conditions. This protection is crucial in multi-step synthetic processes where specific functional groups need to be preserved while other reactions are carried out. Additionally, it is employed in the preparation of sulfonate esters, which are intermediates in the synthesis of various pharmaceuticals and agrochemicals. Its role in facilitating selective reactions makes it valuable in the development of complex organic molecules.

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Test Parameter Specification
Appearance Conforms to Structure
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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inventory 25g
10-20 days ฿35,100.00

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TRIMETHYLSILYLBENZENESULFONATE
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Trimethylsilylbenzenesulfonate is primarily used as a reagent in organic synthesis, particularly in the protection of hydroxyl groups. It acts as a silylating agent, converting alcohols into their corresponding trimethylsilyl ethers, which are more stable and less reactive under certain conditions. This protection is crucial in multi-step synthetic processes where specific functional groups need to be preserved while other reactions are carried out. Additionally, it is employed in the preparation of sulf

Trimethylsilylbenzenesulfonate is primarily used as a reagent in organic synthesis, particularly in the protection of hydroxyl groups. It acts as a silylating agent, converting alcohols into their corresponding trimethylsilyl ethers, which are more stable and less reactive under certain conditions. This protection is crucial in multi-step synthetic processes where specific functional groups need to be preserved while other reactions are carried out. Additionally, it is employed in the preparation of sulfonate esters, which are intermediates in the synthesis of various pharmaceuticals and agrochemicals. Its role in facilitating selective reactions makes it valuable in the development of complex organic molecules.

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