• 1. Evolution of cellulose into flexible conductive green electronics: a smart strategy to fabricate sustainable electrodes for supercapacitors
  Tengfei Yu,Yuehan Wu,Wei Li,Bin Li RSC Adv., 2014,4, 34134-34143
• 2. Fatty acid positional distribution in colostrum and mature milk of women living in Inner Mongolia, North Jiangsu and Guangxi of China?
  Long Deng,Qian Zou,Biao Liu,Wenhui Ye,Chengfei Zhuo,Li Chen,Ze-Yuan Deng,Ya-Wei Fan,Jing Li Food Funct., 2018,9, 4234-4245
• 3. Fe/Fe3C@C nanoparticles encapsulated in N-doped graphene–CNTs framework as an efficient bifunctional oxygen electrocatalyst for robust rechargeable Zn–air batteries?
  Zhiyan Chen,Nan Wu,Yaobing Wang,Bing Wang,Yingde Wang J. Mater. Chem. A, 2018,6, 516-526
• 4. Fast-Track to Research Data Management in Experimental Material Science-Setting the Ground for Research Group Level Materials Digitalization.
  LarsBanko,AlfredLudwig
• 5. Evolution of shape, size, and areal density of a single plane of Si nanocrystals embedded in SiO2 matrix studied by atom probe tomography
  Bin Han,Yasuo Shimizu,Gabriele Seguini,Celia Castro,Gérard Ben Assayag,Koji Inoue,Yasuyoshi Nagai,Sylvie Schamm-Chardon,Michele Perego RSC Adv., 2016,6, 3617-3622

2-[3-[Methyl-bis(trimethylsilyloxy)silyl]propoxy]ethyl acetate: A Comprehensive Overview

2-[3-[Methyl-bis(trimethylsilyloxy)silyl]propoxy]ethyl acetate, identified by the CAS number 125997-17-3, is a highly specialized organic compound with significant applications in various fields. This compound belongs to the class of silyl ethers, which are widely recognized for their unique chemical properties and versatility. The structure of this compound incorporates a methyl group, trimethylsilyloxy groups, and an ethyl acetate moiety, making it a valuable component in modern chemical synthesis and material science.

The synthesis of 2-[3-[Methyl-bis(trimethylsilyloxy)silyl]propoxy]ethyl acetate involves advanced methodologies that ensure high purity and stability. Recent studies have highlighted its role in the development of novel materials, particularly in the realm of organosilicon chemistry. Its ability to form stable silyl ether linkages has made it a preferred choice in the synthesis of bioactive molecules and advanced polymers.

One of the most notable applications of this compound is in the field of organosilicon-based materials. Researchers have demonstrated its potential in creating high-performance coatings and adhesives due to its excellent thermal stability and chemical resistance. Additionally, its use in pharmaceutical intermediates has been explored, where it serves as a protective group for sensitive functional groups during complex syntheses.

The structural integrity of 2-[3-[Methyl-bis(trimethylsilyloxy)silyl]propoxy]ethyl acetate is further enhanced by the presence of trimethylsilyloxy groups, which provide additional stability against hydrolysis. This feature makes it particularly useful in aqueous environments, where maintaining chemical integrity is crucial. Recent advancements in green chemistry have also led to the exploration of this compound as a sustainable alternative in various industrial processes.

In terms of physical properties, this compound exhibits a low melting point and moderate solubility in common organic solvents. Its boiling point is significantly influenced by the silyl ether groups, which contribute to its volatility under certain conditions. These properties make it suitable for applications requiring precise control over reaction conditions, such as in microelectronics and optoelectronics.

The growing demand for high-performance materials has driven extensive research into the optimization of synthesis routes for 2-[3-[Methyl-bis(trimethylsilyloxy)silyl]propoxy]ethyl acetate. Innovations in catalytic systems and reaction engineering have enabled more efficient production methods, reducing costs and improving yield rates. These developments underscore its importance as a key intermediate in contemporary chemical manufacturing.

In conclusion, 2-[3-[Methyl-bis(trimethylsilyloxy)silyl]propoxy]ethyl acetate stands as a testament to the ingenuity of modern chemistry. Its unique combination of structural features and functional properties positions it as an essential component in diverse industries. As research continues to uncover new applications and improvements, this compound will undoubtedly play an even more pivotal role in shaping the future of materials science and chemical engineering.

• 332062-08-5(Fmoc-S-3-amino-4,4-diphenyl-butyric acid)
• 1270529-38-8(1,2,3,4,5,6-Hexahydro-[2,3]bipyridinyl-6-ol)
• 2680771-01-9(4-cyclopentyl-3-{(prop-2-en-1-yloxy)carbonylamino}butanoic acid)
• 2098070-20-1(2-(3-(Pyridin-3-yl)-1H-pyrazol-1-yl)acetimidamide)
• 1444113-98-7(N-(3-cyanothiolan-3-yl)-2-[(2,2,2-trifluoroethyl)sulfanyl]pyridine-4-carboxamide)
• 941977-17-9(N'-(3-chloro-2-methylphenyl)-N-2-(dimethylamino)-2-(naphthalen-1-yl)ethylethanediamide)
• 2138166-62-6(2,2-Difluoro-3-[methyl(2-methylbutyl)amino]propanoic acid)
• 89640-58-4(2-Iodo-4-nitrophenylhydrazine)
• 1449132-38-0(3-Fluoro-5-(2-fluoro-5-methylbenzylcarbamoyl)benzeneboronic acid)
• 2034271-14-0(2-(1H-indol-3-yl)-N-{[6-(thiophen-2-yl)-[1,2,4]triazolo[4,3-b]pyridazin-3-yl]methyl}acetamide)