86053-32-9 Usage
Uses
Used in Silicone Polymer Synthesis:
2,2,4,4,8-pentamethyl-1,5,8,2,4-dioxazadisilecane is used as a precursor in the synthesis of silicone polymers for its ability to contribute to the formation of stable and versatile polymeric materials.
Used in Organosilicon Compounds Production:
In the production of other organosilicon compounds, 2,2,4,4,8-pentamethyl-1,5,8,2,4-dioxazadisilecane serves as a key building block, leveraging its structural and chemical properties to create a range of organosilicon materials with diverse applications.
Used in High-Temperature Applications:
Due to its high thermal stability, 2,2,4,4,8-pentamethyl-1,5,8,2,4-dioxazadisilecane is used in applications that require materials capable of withstanding high temperatures without degrading, such as in the aerospace and automotive industries.
Used in Oxidation-Resistant Coatings:
The resistance to oxidation of 2,2,4,4,8-pentamethyl-1,5,8,2,4-dioxazadisilecane makes it suitable for use in the development of coatings that protect materials from oxidative damage, extending their service life in various industrial settings.
Check Digit Verification of cas no
The CAS Registry Mumber 86053-32-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,0,5 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 86053-32:
(7*8)+(6*6)+(5*0)+(4*5)+(3*3)+(2*3)+(1*2)=129
129 % 10 = 9
So 86053-32-9 is a valid CAS Registry Number.
86053-32-9Relevant academic research and scientific papers
Atrane Analogous Compounds of Type (I)
Grobe, Joseph,Voulgarakis, Nikolaos
, p. 269 - 279 (2007/10/02)
Heterocyclic ring compounds of type I (compounds 9 and 10) have been prepared by condensation reactions of α,ω-difunctional derivatives XMe2SiCH2M'Me2X (X = Cl, NMe2; M' = Si, Sn) with N-methyldiethanolamine using the "Dilution Principle".The starting compounds XMe2SiCH2M'Me2X are obtained by reacting XMe2SiCH2MgCl with ClM'Me2X (Scheme, Abb. 1).The existence of transanular N->Si or N->M' interactions depends on the N-M distance and the acidity of the acceptor atoms.In order to clarify the weight of these factors acyclic analoga of compounds 9 and 10 have been prepared. - Key words: Silatrane, Stannatrane, Transanular N -> M - Interaction, NMR Data
