80907-11-5 Usage
Uses
Used in Chemical Reactions:
1,1,1-triethyl-3,3-dimethyldisiloxane is used as a solvent and a reagent in various chemical reactions due to its stability and compatibility with other chemicals.
Used in Electronic Device Production:
1,1,1-triethyl-3,3-dimethyldisiloxane is used as a protective coating in the production of electronic devices, providing a protective layer that helps to prevent damage and enhance the performance of the devices.
Used in Silicone Rubber Manufacturing:
1,1,1-triethyl-3,3-dimethyldisiloxane is used as a crosslinking agent in the manufacturing of silicone rubber, improving the strength and durability of the rubber.
Used in Coatings and Paints:
1,1,1-triethyl-3,3-dimethyldisiloxane is used in coatings and paints due to its low surface tension and good spreading properties, which help to create a smooth and even finish.
Used in Industrial and Commercial Applications:
1,1,1-triethyl-3,3-dimethyldisiloxane has a wide range of industrial and commercial uses due to its stability and compatibility with other chemicals and materials, making it a versatile compound for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 80907-11-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,9,0 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 80907-11:
(7*8)+(6*0)+(5*9)+(4*0)+(3*7)+(2*1)+(1*1)=125
125 % 10 = 5
So 80907-11-5 is a valid CAS Registry Number.
80907-11-5Relevant academic research and scientific papers
On the Problem of the Intermediate Formation of Silanone R2Si=O by Reactions of Silenes with Dinitrogen Oxide
Wiberg, Nils,Preiner, Gerhard,Schurz, Klaus
, p. 1407 - 1412 (2007/10/02)
The silaethene Me2Si=C(SiMe3)2 (1a; unstable; from 1a * Ph2C=MSiMe3 = 4) forms with N2O an unstable cycloadduct, which decomposes under isomerization or cleavage.It was not possible to decide clearly, whether the last reaction, which leads to (Me3Si)2CN2 and polymers with (Me2SiO)n groups, proceeds with intermediate formation of silanone Me2Si=O or not (no trapping product with Et3SiH, but with Me3SiCl).The silanimines Me2Si=NSitBu3 (2a; unstable; from 2a * tBu3SiN3 = 7) and tBu2Si=NSitBu3 (2b; metastable) form with N2O unstable cycloadducts, which, under participation of the silanimines, react into products (10) being composed of a molecular silanone and a molecule silanimine.As has been shown by trapping experiments with Et3SiH, Me3SiCl, or Me3SiOMe, latter reaction involves unstable free silanones Me2Si=O (3a) or tBuSi=O (3b) as intermediates. 3b, generated in benzene from 2b/NO2 in the presence of equimolar amounts of tetrahydrofuran (THF), obviously forms an adduct 3b*THF, which is trapped by excess 2b.When 3b is produced in THF as solvent, the silanone starts THF polymerization, indicating a high Lewis acidity of silanones.
