10124-62-6 Usage
Description
1,2-DIMETHOXY-1,1,2,2-TETRAMETHYLDISILANE is an organosilane compound characterized by its symmetrical structure and two methoxy groups attached to the silicon atom. It is known for its stability and reactivity in various chemical reactions, making it a versatile compound in the field of organic chemistry and materials science.
Uses
Used in Sol-Gel Chemistry:
1,2-DIMETHOXY-1,1,2,2-TETRAMETHYLDISILANE is used as a precursor in the palladium-catalyzed bis(silylation) of 1,4-diethynylbenzene. This application is significant because it allows for the creation of a crack-free sol-gel, which is crucial for the development of high-quality materials with specific properties and applications.
Used in Chemical Synthesis:
1,2-DIMETHOXY-1,1,2,2-TETRAMETHYLDISILANE is used as a starting material to prepare dimethylsilylene via gas-phase flow-pyrolysis at 600°C. This process is essential in the synthesis of various organosilane compounds and materials with unique properties, such as improved thermal stability, chemical resistance, and mechanical strength.
Used in Coatings and Adhesives Industry:
1,2-DIMETHOXY-1,1,2,2-TETRAMETHYLDISILANE can be used as a component in the formulation of coatings and adhesives, where its organosilane nature contributes to enhanced adhesion, durability, and resistance to environmental factors.
Used in Electronic Materials:
In the electronics industry, 1,2-DIMETHOXY-1,1,2,2-TETRAMETHYLDISILANE can be employed in the development of materials with specific electrical and thermal properties, such as insulators, semiconductors, or components in microelectronic devices.
Used in Pharmaceutical and Biomedical Applications:
Due to its unique chemical structure, 1,2-DIMETHOXY-1,1,2,2-TETRAMETHYLDISILANE may also find applications in the pharmaceutical and biomedical fields, potentially serving as a building block for the development of new drugs or materials with specific biological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 10124-62-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,1,2 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10124-62:
(7*1)+(6*0)+(5*1)+(4*2)+(3*4)+(2*6)+(1*2)=46
46 % 10 = 6
So 10124-62-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H18O2Si2/c1-7-9(3,4)10(5,6)8-2/h1-6H3
10124-62-6Relevant articles and documents
Photoinduced electron-transfer reaction of 7,8- disilabicyclo[2.2.2]octa-2,5-dienes
Kako,Hatakenaka,Kakuma,Ninomiya,Nakadaira,Yasui,Iwasaki,Wakasa,Hayashi
, p. 1133 - 1136 (2007/10/03)
9,10-Dicyanoanthracene-sensitized irradiation of 7,8- disilabicyclo[2.2.2]octa-2-5-dienes1-3 in the presence of MeOH resulted in the formation of dimethoxydisilanes and the corresponding aromatic compounds. A stepwise mechanism involving C-Si bond cleavage by MeOH is proposed.
Synthesis and reactions of silanes containing two triflate groups
Matyjaszewski, K.,Chen, Y. L.
, p. 7 - 12 (2007/10/02)
1,2-Bis(trifluoromethanesulfonyloxy)tetramethyldisilane (1) and dimethylsilylbis(trifluoromethanesulfonate) (2) have been prepared via displacement of phenyl, chloro, and methyl groups in the corresponding mono- and di-silanes.Phenyl groups are displaced more rapidly than chloro and methyl groups.The unreacted groups are strongly deactivated by the presence of a triflate group at the same silicon atom.The deactivation is much weaker when a triflate group is present at the adjacent silicon atom.Alcohols and amines react more rapidly with ditriflates than with monotriflates.
