18157-17-0 Usage
Description
2-Chloroethoxytrimethylsilane is a colorless liquid chemical compound with the molecular formula C5H12ClOSi, characterized by a strong odor and high flammability. It is a versatile silane coupling agent and intermediate, playing a crucial role in various industrial applications.
Uses
Used in Chemical Industry:
2-Chloroethoxytrimethylsilane is used as a coupling agent for enhancing the bonding between glass fibers and siliceous materials, which significantly improves the strength and durability of composite materials.
Used in Silicone Production:
It serves as an intermediate in the production of silicone resins, which are essential components in the manufacturing of coatings and adhesives.
Used in Manufacturing Industry:
2-Chloroethoxytrimethylsilane is utilized as a processing aid in the manufacturing of various industrial products, contributing to the improvement of their overall quality and performance.
However, due to its corrosive nature and potential to cause severe eye irritation, it is imperative to handle 2-Chloroethoxytrimethylsilane with care and store it in a cool, well-ventilated area away from heat and incompatible materials.
Check Digit Verification of cas no
The CAS Registry Mumber 18157-17-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,5 and 7 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 18157-17:
(7*1)+(6*8)+(5*1)+(4*5)+(3*7)+(2*1)+(1*7)=110
110 % 10 = 0
So 18157-17-0 is a valid CAS Registry Number.
InChI:InChI=1/C5H13ClOSi/c1-8(2,3)7-5-4-6/h4-5H2,1-3H3
18157-17-0Relevant articles and documents
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.
REACTION OF 2-METHYL-2-PHENYL-1,3-DIOXOLANE WITH TRIMETHYLCHLOROSILANE
Musavirov, R. S.,Mullakhmetova, Z. F.,Nedogrei, E. P.,Kantor, E. A.,Rakmankulov, D. L.
, p. 1297 - 1298 (2007/10/02)
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PROTECTION OF ALCOHOLS AND ACIDS WITH ALLYLSILANES CATALYZED BY IODINE OR IODOTRIMETHYLSILANE IN CHLORINATED HYDROCARBON
Hosomi, Akira,Sakurai, Hideki
, p. 85 - 88 (2007/10/02)
Many triorganosilyl ethers and esters were prepared by the reaction of allylsilanes with alcohols catalyzed by iodine or iodotrimethylsilane in excellent yields.Bromine and bromotrimethylsilane were also effective catalysts.
