56929-77-2

Usage

Uses

Used in Chemical Synthesis:
2-(2,8,9-Trioxa-5-aza-1-silabicyclo[3.3.3]undec-1-yloxy)ethanol is utilized as a precursor in the synthesis of a variety of organic compounds and materials. Its unique structural features, including the silicon bridge, make it a valuable component in creating new molecules with specific properties for various applications.
Used in Materials Science:
In the field of materials science, 2-(2,8,9-Trioxa-5-aza-1-silabicyclo[3.3.3]undec-1-yloxy)ethanol is used as a building block for developing novel materials. The incorporation of silicon in its structure can enhance material properties such as stability, reactivity, or specific interactions with other elements or compounds.
Used in Pharmaceutical Research:
2-(2,8,9-Trioxa-5-aza-1-silabicyclo[3.3.3]undec-1-yloxy)ethanol is also used in pharmaceutical research as a potential candidate for drug development. Its complex structure may offer new avenues for the design of pharmaceutical agents, particularly those that require specific interactions with biological targets due to the presence of the silicon atom.
Used in Silicon-Containing Compounds Development:
2-(2,8,9-Trioxa-5-aza-1-silabicyclo[3.3.3]undec-1-yloxy)ethanol is employed in the development of silicon-containing compounds, which have a wide range of applications in various industries. The silicon atom in 2-(2,8,9-Trioxa-5-aza-1-silabicyclo[3.3.3]undec-1-yloxy)ethanol can provide unique reactivity and properties that are not found in purely organic compounds.
Used in Controlled Laboratory Settings:
Due to its complex structure and potential reactivity, 2-(2,8,9-Trioxa-5-aza-1-silabicyclo[3.3.3]undec-1-yloxy)ethanol is used with caution in controlled laboratory settings. This ensures the safety of researchers and the integrity of experiments involving 2-(2,8,9-Trioxa-5-aza-1-silabicyclo[3.3.3]undec-1-yloxy)ethanol.

InChI:InChI=1/C8H17NO5Si/c10-4-8-14-15-9(1-5-11-15,2-6-12-15)3-7-13-15/h10H,1-8H2

Upstream product

• 102-71-6 triethanolamine 
• 107-21-1 ethylene glycol 

Relevant academic research and scientific papers

Neutral alkoxysilanes from silica

Silica (SiO2) is found to react readily with ethylene glycol (EGH2) to form neutral glycoxysilanes in the presence of catalytic amounts of high-boiling organic amines, such as triethylenetetramine (TETA), trishydroxymethyleneaminomethane [H2NC(CH2OH)3, THAMH3], and triethanolamine [N(CH2CH2OH)3, TEAH3]. Kinetic studies show that these amines offer similar catalytic efficiencies although their pKb values differ by 3 orders of magnitude. In addition, silica dissolution is found to be pseudo-zero order in silica. These kinetic data can be explained by a rate-limiting step involving release of free base from an intermediate pentacoordinated silicate coincident with the formation of a tetraalkoxysilane. The products from these reactions were characterized by 1H, 13C, and 29Si solution and solid-state NMR, thermal gravimetric analysis, and mass spectroscopy. Depending on the type and amount of base used, different products form: either neutral tetraalkoxysilanes, such as Si(OCH2CH2OH)4 and its soluble oligomers, or neutral pentacoordinate silanes, such as N(CH2CH2O)3SiOCH2CH2OH and H3N+C(CH2O)3Si-(OCH 2CH2O). Comparative studies demonstrate that Group I metal hydroxides also catalyze silica dissolution in ethylene glycol with better catalytic efficiencies than the amine bases. The products of silica dissolution using Group I metal hydroxide catalysts were also identified by 29Si solution NMR and mass spectroscopy and found to consist primarily of Si(OCH2CH2OH)4 and its oligomeric derivatives.