![]() 三甲基乙氧基硅烷结构式
|
常用名 | 三甲基乙氧基硅烷 | 英文名 | Ethoxy(trimethyl)silane |
---|---|---|---|---|
CAS号 | 1825-62-3 | 分子量 | 118.250 | |
密度 | 0.8±0.1 g/cm3 | 沸点 | 75.5±0.0 °C at 760 mmHg | |
分子式 | C5H14OSi | 熔点 | -83°C | |
MSDS | 中文版 美版 | 闪点 | -18.9±0.0 °C | |
符号 |
![]() ![]() GHS02, GHS07 |
信号词 | Danger |
Silanization-Based Zeolite Crystallization: Participation Degree and Pathway.
Chemistry 21 , 12161-70, (2015) A clear and deep understanding of zeolite crystallization with the addition of organosilane is desirable for the reasonable design and preparation of hierarchical zeolites. Herein, the effects of different organosilanes on zeolite crystallization were systema... |
|
Properties of short double-stranded RNAs carrying randomized base pairs: toward better controls for RNAi experiments.
RNA 21 , 2132-42, (2015) Short interfering RNAs (siRNAs) are mediators of RNA interference (RNAi), a commonly used technique for selective down-regulation of target gene expression. Using an equimolar mixture of A, G, C, and U phosphoramidites during solid-phase synthesis, we introdu... |
|
29Si NMR of ethoxytrimethylsilane hydrolysis and sodium ion exchange. Suda S, et al.
J. Non. Cryst. Solids 176(1) , 26-32, (1994)
|
|
Structural and photophysical properties of rare-earth complexes encapsulated into surface modified mesoporous silica nanoparticles. Malba C, et al.
Dalton Trans. 43(43) , 16183-16196, (2014)
|
|
Regiospecific synthesis of α-lithiated alkoxysilanes. Bates TF, et al.
J. Organomet. Chem. 595(1) , 87-92, (2000)
|
|
Electron Moments and Structures of Organosilicon Compounds. III. The Oxygen-Silicon Bond1, 2. Freiser H, et al.
J. Am. Chem. Soc. 75(12) , 2824-2827, (1953)
|
|
Alkylation of isobutane/1-butene on methyl-modified Nafion/SBA-15 materials. Shen W, et al.
Appl. Catal. A Gen. 377(1) , 1-8, (2010)
|
|
Surface chemistry and trimethylsilyl functionalization of Stöber silica sols. Suratwala TI, et al.
J. Non. Cryst. Solids 316(2) , 349-363, (2003)
|
|
Part I. Dichloro-and dibromotrimethylsiloxyaluminium: structure, and reaction with sodium acetylacetonate. Ercolani CA, et al.
J. Chem. Soc. , 603-605, (1966)
|