18230-61-0 Usage
Uses
Used in Adhesives, Sealants, and Coatings Industry:
Diisopropyldimethoxysilane is used as a coupling agent to enhance the bonding between organic and inorganic materials, thereby improving the moisture resistance and increasing the durability and strength of adhesives, sealants, and coatings.
Used in Silicone Rubber and Silicone-based Products Manufacturing:
In the production of silicone rubber and other silicone-based products, Diisopropyldimethoxysilane serves as a key component that contributes to the improvement of the final product's properties, including its flexibility, thermal stability, and resistance to environmental factors.
Used in Surface Treatment Formulation for Glass, Metal, and Plastic Industries:
Diisopropyldimethoxysilane is used as a surface modifier in the formulation of treatments for glass, metal, and plastic surfaces. It improves the adhesion and compatibility of these surfaces with other materials, ensuring a stronger bond and better integration in various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 18230-61-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,2,3 and 0 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 18230-61:
(7*1)+(6*8)+(5*2)+(4*3)+(3*0)+(2*6)+(1*1)=90
90 % 10 = 0
So 18230-61-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H20O2Si/c1-7(2)11(9-5,10-6)8(3)4/h7-8H,1-6H3
18230-61-0Relevant academic research and scientific papers
Versatile method for introduction of bulky substituents to alkoxychlorosilanes
Masaoka, Shin,Banno, Tadashi,Ishikawa, Mitsuo
, p. 182 - 192 (2007/10/03)
The reactions of various alkoxytrichlorosilanes prepared in situ from tetrachlorosilane and alcohols, with Grignard reagents bearing a bulky substituent such as the isopropyl, sec-butyl, and cyclohexyl group afforded triisopropyl-, tri(sec-butyl)-, and tricyclohexylalkoxysilane in high yields. The reactions of n-butoxytrichlorosilane with these Grignard reagents produced triisopropyl-, tri(sec-butyl)-, and tricyclohexyl(n-butoxy)silane in 94%, 96%, and 92% yields, respectively. Methoxymethyldichlorosilane reacted with the same Grignard reagents to give diisopropyl-, di(sec-butyl)-, and dicyclohexylmethoxymethylsilane in 84%, 83%, and 83% yields. Treatment of methoxydimethylchlorosilane with the Grignard reagents readily afforded isopropyl-, sec-butyl-, and cyclohexylmethoxydimethylsilane in excellent yields. Similar treatment of methoxydimethylchlorosilane with tert-butylmagnesium chloride gave tert-butylmethoxydimethylsilane in 62% yield.
Methods for producing diorganodialkoxysilanes
-
, (2008/06/13)
In a method for the selective production of diorganodialkoxysilanes of the general formula STR1 by reaction of tetraalkoxysilanes of the formula Si(OR3)4 and monoorganotrialkoxysilanes of the formula R1 Si(OR3)
