18173-74-5 Usage
Description
(2-methoxyethoxy)trimethylsilane is a clear, colorless liquid that belongs to the organosilicon compound family. It is commonly used as a coupling agent and adhesion promoter in various industrial applications, such as in the production of coatings, adhesives, and sealants. This chemical compound is known for its ability to improve the bonding between organic and inorganic materials, making it a valuable component in the formulation of polymers and composite materials. Additionally, (2-methoxyethoxy)trimethylsilane is also used as a surface modifier to enhance the hydrophobicity and oleophobicity of surfaces, making it a versatile and important chemical in the manufacturing and construction industries.
Uses
Used in Coatings Industry:
(2-methoxyethoxy)trimethylsilane is used as a coupling agent and adhesion promoter for improving the bonding between organic and inorganic materials in the formulation of coatings.
Used in Adhesives Industry:
(2-methoxyethoxy)trimethylsilane is used as a coupling agent and adhesion promoter for enhancing the bonding between organic and inorganic materials in the production of adhesives.
Used in Sealants Industry:
(2-methoxyethoxy)trimethylsilane is used as a coupling agent and adhesion promoter for improving the bonding between organic and inorganic materials in the formulation of sealants.
Used in Polymer and Composite Materials Industry:
(2-methoxyethoxy)trimethylsilane is used as a component in the formulation of polymers and composite materials to improve the bonding between organic and inorganic materials.
Used in Surface Modification:
(2-methoxyethoxy)trimethylsilane is used as a surface modifier to enhance the hydrophobicity and oleophobicity of surfaces in the manufacturing and construction industries.
Check Digit Verification of cas no
The CAS Registry Mumber 18173-74-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,7 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 18173-74:
(7*1)+(6*8)+(5*1)+(4*7)+(3*3)+(2*7)+(1*4)=115
115 % 10 = 5
So 18173-74-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H16O2Si/c1-7-5-6-8-9(2,3)4/h5-6H2,1-4H3
18173-74-5Relevant articles and documents
Highly conductive trimethylsilyl oligo(ethylene oxide) electrolytes for energy storage applications
Zhang, Lingzhi,Zhang, Zhengcheng,Harring, Scott,Straughan, Megan,Butorac, Rachel,Chen, Zonghai,Lyons, Leslie,Amine, Khalil,West, Robert
, p. 3713 - 3717 (2008)
Monomethyl ethers of oligoethylene glycols with different chain lengths were converted to trimethylsilyl derivatives by reacting with trimethylchlorosilane in the presence of triethylamine, or by directly refluxing with excess trimethylchlorosilane or hex
Glycosyl Fluorides as Intermediates in BF3·OEt2-Promoted Glycosylation with Trichloroacetimidates
Nielsen, Michael M.,Stougaard, Bolette A.,Bols, Mikael,Glibstrup, Emil,Pedersen, Christian M.
supporting information, p. 1281 - 1284 (2017/03/17)
Glycosyl fluorides have been found to be important intermediates in glycosylations with trichloroacetimidate donors and BF3·OEt2 activation (0.2–1 equiv.). Low-temperature NMR spectroscopy experiments revealed that the α-trichloroacetimidate was transformed into the glycosyl fluoride with inversion of stereochemistry, whereas the β anomer was not. A concerted mechanism was suggested for the stereospecific formation of glycosyl fluorides, which is not accounted for in the classic mechanism.
Silicon-29 NMR spectra of trimethylsilylated alcohols
Kvicalova, Magdalena,Cermak, Jan,Blechta, Vratislav,Schraml, Jan
, p. 816 - 820 (2007/10/03)
29Si NMR spectra of trimethylsilyl (TMS) derivatives of 26 simple alcohols were measured under standardized conditions (i.e., in sufficiently diluted deuteriochloroform solutions). Due to association with the solvent the chemical shifts are in almost all cases larger than those reported earlier for different solutions. This observation is in agreement with the proposed mechanism of steric effects as being due to sterically controlled association with the solvent. The use of chloroform as a solvent enhances steric effects hut at the same time it can reduce small differences due to polar effects in closely related compounds. In the studied class of compounds the gross dependence of the chemical shift on polar effects is not substantially affected by the change of the solvent.