97203-62-8

Usage

Uses

Used in Organic Synthesis:
2-(Trimethylsilyl)ethanol is used as a reagent for the preparation of silyl ethers, which serve as protecting groups in organic chemistry. This application is crucial for the synthesis of complex organic molecules, as it allows chemists to temporarily mask functional groups during reactions, preventing unwanted side reactions.
Used in Pharmaceutical and Agrochemical Industries:
2-(Trimethylsilyl)ethanol is used as a building block in the synthesis of various organic compounds, including pharmaceuticals and agrochemicals. Its ability to stabilize reactive intermediates and serve as a versatile starting material makes it an essential component in the development of new drugs and agricultural chemicals.
Used in the Production of Functionalized Compounds:
2-(Trimethylsilyl)ethanol is utilized as a starting material for the production of a wide range of functionalized compounds. Its unique properties and reactivity make it a valuable resource in the synthesis of various specialty chemicals, contributing to the advancement of chemical research and development.

InChI:InChI=1/C5H14OSi/c1-7(2,3)5-4-6/h6H,4-5H2,1-3H3

Upstream product

• 97203-61-7 1-trimethylsilylethanesulfonic acid 
• 18143-52-7 1-trimethylsilylethanethiol 
• 7787-87-3 (1-chloroethyl)trimethylsilane 

Relevant academic research and scientific papers

Synthesis of Methanethial S-Oxide (Sulfine) and Alkanethial S,S-Dioxides by Fluorodesilylation. Stereochemistry of Their Cyclopentadiene Diels-Alder Adducts

Fluorodesilylation of trimethylsilylmethanesulfinyl chloride 4 in the presence of cyclopentadiene gives 2-thiabicyclohept-5-ene endo-2-oxide, 5; in a like manner 1-trimethylsilylalkanesulfonic anhydrides afford endo- and exo-3-alkyl-2-thiabicyclohept-5-ene 2,2-dioxides, with the endo isomer predominating.Sulfine and alkyl sulfenes are invoked.