Acetyltrimethylsilane

95%

Reagent Code: #88391
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CAS Number 13411-48-8

science Other reagents with same CAS 13411-48-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 116.23 g/mol
Formula C₆H₁₂OSi
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MDL Number MFCD00134244
inventory_2 Storage & Handling
Density 0.811 g/mL at 25 °C (lit.)
Storage 2-8°C, dry, away from light

description Product Description

Acetyltrimethylsilane is primarily used in organic synthesis as a reagent for introducing the trimethylsilyl group into molecules. This group serves as a protecting group for alcohols and other functional groups, enhancing stability during chemical reactions. It is also employed in the preparation of silyl enol ethers, which are intermediates in various organic transformations, including aldol reactions and Michael additions. Additionally, it finds application in the modification of surfaces and materials, where it imparts hydrophobic properties. Its use extends to the synthesis of silicon-containing polymers and in the production of specialty chemicals for the pharmaceutical and agrochemical industries.

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Test Parameter Specification
Appearance light yellow liquid
Purity 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿5,100.00
inventory 5g
10-20 days ฿23,650.00

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Acetyltrimethylsilane
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Acetyltrimethylsilane is primarily used in organic synthesis as a reagent for introducing the trimethylsilyl group into molecules. This group serves as a protecting group for alcohols and other functional groups, enhancing stability during chemical reactions. It is also employed in the preparation of silyl enol ethers, which are intermediates in various organic transformations, including aldol reactions and Michael additions. Additionally, it finds application in the modification of surfaces and material

Acetyltrimethylsilane is primarily used in organic synthesis as a reagent for introducing the trimethylsilyl group into molecules. This group serves as a protecting group for alcohols and other functional groups, enhancing stability during chemical reactions. It is also employed in the preparation of silyl enol ethers, which are intermediates in various organic transformations, including aldol reactions and Michael additions. Additionally, it finds application in the modification of surfaces and materials, where it imparts hydrophobic properties. Its use extends to the synthesis of silicon-containing polymers and in the production of specialty chemicals for the pharmaceutical and agrochemical industries.

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