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Usage

Uses

Used in Organic Synthesis:
(2-Bromoethyl)trimethylsilane is utilized as a reagent in organic synthesis, specifically for the preparation of organosilicon compounds. Its reactivity allows for the formation of a wide range of products that can be further used in different applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (2-Bromoethyl)trimethylsilane serves as a precursor for the synthesis of functionalized organosilicon compounds. These compounds can possess unique properties that make them valuable in the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, (2-Bromoethyl)trimethylsilane is employed as a starting material for the creation of organosilicon compounds that can be used in the formulation of pesticides, herbicides, and other agricultural chemicals.
Used in Materials Industry:
The materials industry also benefits from the use of (2-Bromoethyl)trimethylsilane as a precursor for synthesizing organosilicon compounds with specific material properties. These can be used in the development of new materials with applications in various sectors, such as electronics, construction, and automotive.
Safety Considerations:
It is important to handle (2-Bromoethyl)trimethylsilane with care due to its potential hazards, including flammability and toxicity. Proper safety measures and precautions should be taken during its use to minimize risks.

InChI:InChI=1/C5H13BrSi/c1-7(2,3)5-4-6/h4-5H2,1-3H3

Upstream product

• 2916-68-9 2-(Trimethylsilyl)ethanol 
• 754-05-2 ethenyltrimethylsilane 

Downstream Products

• 54288-07-2 3-(Trimethylsilanyl)-1-phenylpropan-1-ol 
• 84673-74-5 1,1-Diphenyl-4-(trimethylsilyl)-1-buten 
• 439675-13-5 diselenobenzoic acid Se-2-(trimethylsilyl)ethyl ester 
• 439675-14-6 2-methyldiselenobenzoic acid Se-2-(trimethylsilyl)ethyl ester 
• 439675-15-7 4-bromodiselenobenzoic acid Se-2-(trimethylsilyl)ethyl ester 
• 439675-16-8 4-methoxydiselenobenzoic acid Se-2-(trimethylsilyl)ethyl ester 
• 36058-43-2 Trimethylethylsilanradikal 
• 2117-37-5 tri-n-butylgermanium bromide 
• 1220904-60-8 C₂₀H₃₅NO₃SSi 
• 1220904-59-5 C₂₀H₃₅NO₃SSi 
• 1336889-08-7 C₁₆H₂₇NO₂Si*ClH 
• 91176-30-6 trimethyl(3-(p-tolyl)but-3-en-1-yl)silane 
• 1228173-20-3 1,4-benzenedicarbodithioic acid 2-(trimethlysilyl)ethyl ester 
• 86498-78-4 (E)-1-(2-Isopropenyl-4-methoxy-phenyl)-4-(2-trimethylsilanyl-ethyl)-hexa-3,5-dien-1-ol 

Relevant academic research and scientific papers

Thiolate chemistry: A powerful and versatile synthetic tool for immobilization/functionalization of oligothiophenes on a gold surface

The synthesis and characterization of a series of quaterthiophenes (4Ts) with thiolate groups protected with 2-cyanoethyl (CNE), 2-trimethylsilylethyl (TMSE), and acetyl (Ac) groups are described. Sequential cleavage of these different protecting groups allows for the preparation of 4Ts derivatized with ferrocene and/or alkanethiol chains. The electrochemical behavior of these compounds has been analyzed in solution by cyclic voltammetry (CV). A ferrocene-derivatized dithiol 4T 14 and a dithiol 4T 15 with two TMSE-protected thiolate groups have been immobilized on a gold surface as monolayers that have been characterized by CV, ellipsometry, contact-angle measurement, and X-ray photoelectron spectroscopy (XPS). The results show that molecules 14 and 15 are doubly grafted with a horizontal orientation of the conjugated system relative to the surface. Furthermore, application of the deprotection/alkylation sequence of the remaining protected thiolate groups on a monolayer of 15 allows for efficient post-functionalization.

The first ammonium aromatic diselenoates: Stable heavy congeners of aromatic carboxylic acid salts

Ammonium aromatic diselenoates were synthesized by reacting aromatic diselenoic acid 2-(trimethylsilyl)ethyl esters derived from aluminum 2-(trimethylsilyl)ethyl selenolate with aromatic selenoic acid O-methyl esters with ammonium fluorides. The results o