5290-24-4 Usage
General Description
3-Acetoxypropyl methyl dichlorosilane is a chemical compound with the molecular formula C6H13Cl2O2Si. It is used as a silane coupling agent in various industrial applications, including the production of adhesives, coatings, and sealants. 3-ACETOXYPROPYL METHYL DICHLOROSILANE is synthesized by reacting methyltrichlorosilane with acetoxypropyl chloride. It acts as a reactive adhesion promoter and surface modifier, improving the adhesion between certain substrates and organic resins or polymers. Additionally, 3-acetoxypropyl methyl dichlorosilane is also used in the manufacturing of polysilanes and as a crosslinking agent in silicone elastomers. Due to its ability to improve the mechanical and thermal properties of materials, this compound is valuable in the production of various industrial products.
Check Digit Verification of cas no
The CAS Registry Mumber 5290-24-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,9 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5290-24:
(6*5)+(5*2)+(4*9)+(3*0)+(2*2)+(1*4)=84
84 % 10 = 4
So 5290-24-4 is a valid CAS Registry Number.
InChI:InChI=1/C5H9Cl3O2Si/c1-5(9)10-3-2-4-11(6,7)8/h2-4H2,1H3
5290-24-4Relevant articles and documents
Mechanistic insights into the hydrosilylation of allyl compounds - Evidence for different coexisting reaction pathways
Gigler, Peter,Drees, Markus,Riener, Korbinian,Bechlars, Bettina,Herrmann, Wolfgang A.,Kuehn, Fritz E.
, p. 1 - 14 (2013/01/14)
The hydrosilylation of allyl compounds is often accompanied by the formation of high amounts of byproducts. The formation processes have not been fully understood so far. In this work, the allyl hydrosilylation mechanism is investigated in detail and experimental and theoretical evidence for multiple, coexisting reaction pathways is provided. Based on earlier reports and the observations during an extensive catalytic study, different pathways, leading to the observed byproducts, were identified and proven by labeling experiments and DFT calculations. Oxidative addition of the silane and the insertion of the allyl compound into the Pt-H bond turned out to be the crucial, selectivity-determining steps within the catalytic cycle. Based on these findings, it should be possible to systematically influence these steps and pave the way to a rational and straightforward design of more selective catalysts.
