90633-16-2 Usage
Uses
Used in Adhesives and Sealants Industry:
DIISOPROPYLETHOXYSILANE is used as an adhesion promoter for enhancing the bonding strength between organic and inorganic materials in adhesives and sealants. It improves the durability and performance of the final product by forming a strong bond between different materials.
Used in Coatings Industry:
In the coatings industry, DIISOPROPYLETHOXYSILANE is used as a coupling agent to improve the adhesion of coatings to various substrates, including plastics, rubber, and glass. This results in coatings with better durability and resistance to environmental factors.
Used in Surface Modification:
DIISOPROPYLETHOXYSILANE is used as a surface modifier to enhance the water and oil resistance of materials. By altering the surface properties, it provides improved resistance to water and oil, making the materials more suitable for specific applications.
Overall, DIISOPROPYLETHOXYSILANE plays a crucial role in various industries by improving the adhesion, bonding, and surface properties of materials, leading to enhanced performance and durability of the final products.
Check Digit Verification of cas no
The CAS Registry Mumber 90633-16-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,6,3 and 3 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 90633-16:
(7*9)+(6*0)+(5*6)+(4*3)+(3*3)+(2*1)+(1*6)=122
122 % 10 = 2
So 90633-16-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H20OSi/c1-6-9-10(7(2)3)8(4)5/h7-8,10H,6H2,1-5H3
90633-16-2Relevant articles and documents
Synthesis, characterization, and photoreactions of 1,2-disiladigermacyclobutane
Hashimoto, Hisako,Yagihashi, Yusuke,Ignatovich, Lubov,Kira, Mitsuo
, p. 398 - 405 (2001)
A new four-membered ring compound having a Si2Ge2 skeleton, octaisopropyl-1,2-disiladigermacyclobutane (1), was synthesized by the reductive coupling of tetraisopropyl-1,2-dichlorosilagermane with sodium in toluene. The structure of 1, which has one Ge-Ge bond, one Si-Si bond, and two Ge-Si bonds in a ring; was confirmed by chemical derivatization; the reactions of 1 with m-chloroperoxy-benzoic acid and PCl5 led to the selective cleavage of the Ge-Ge bond in 1. The selective extrusion of a germylene from 1 was observed at the initial stage of the photolysis using 254 nm light.
The Photolysis of Octaisopropylcyclotetrasilane; Evidence for the Formation of Hexaisopropylcyclotrisilane and Tetraisopropyldisilene
Watanabe, Hamao,Kougo, Yuichi,Nagai, Yoichiro
, p. 66 - 67 (2007/10/02)
Irradiation of octaisopropylcyclotetrasilane (1) in a hydrocarbon solvent successively afforded hexaisopropylcyclotrisilane i2Si>3 (2) (λmax 320 nm) and tetraisopropyldisilene i2Si=SiPri2> (3) (λmax 400 nm) with extrusion of di-isopropylsilanediyl (4).
