7671-19-4 Usage
Uses
Used in the Manufacturing Industry:
BIS(TRIMETHYLSILOXY)METHYLMETHOXYSILANE is used as a coupling agent for improving the bonding and compatibility between inorganic fillers and organic polymers in the production of silicone rubber, sealants, and adhesives. This enhances the mechanical properties and durability of the final products.
Used in Surface Modification:
BIS(TRIMETHYLSILOXY)METHYLMETHOXYSILANE is used as a surface modification agent for glass, metal, and other inorganic materials. It provides improved adhesion, moisture resistance, and corrosion resistance, making the materials more suitable for various applications.
Used in the Automotive Industry:
In the automotive industry, BIS(TRIMETHYLSILOXY)METHYLMETHOXYSILANE is used as a component in the production of sealants and adhesives for automotive parts, ensuring strong bonding and durability under various environmental conditions.
Used in the Construction Industry:
BIS(TRIMETHYLSILOXY)METHYLMETHOXYSILANE is used in the construction industry for surface treatment of glass, metal, and other inorganic materials, improving their adhesion to organic materials and enhancing their resistance to moisture and corrosion, which is crucial for the longevity and performance of construction materials.
Used in the Electronics Industry:
In the electronics industry, BIS(TRIMETHYLSILOXY)METHOXYSILANE is used for surface modification of electronic components, improving their adhesion to other materials and enhancing their resistance to moisture and corrosion, which is essential for the reliability and performance of electronic devices.
Check Digit Verification of cas no
The CAS Registry Mumber 7671-19-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,6,7 and 1 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7671-19:
(6*7)+(5*6)+(4*7)+(3*1)+(2*1)+(1*9)=114
114 % 10 = 4
So 7671-19-4 is a valid CAS Registry Number.
InChI:InChI=1/C8H24O3Si3/c1-9-12-8(10-13(2,3)4)11-14(5,6)7/h8H,12H2,1-7H3
7671-19-4Relevant academic research and scientific papers
Selective C-O Bond Reduction and Borylation of Aryl Ethers Catalyzed by a Rhodium-Aluminum Heterobimetallic Complex
Hara, Naofumi,Nakao, Yoshiaki,Saito, Teruhiko,Seki, Rin
supporting information, p. 6388 - 6394 (2021/05/31)
We report the catalytic reduction of a C-O bond and the borylation by a rhodium complex bearing an X-Type PAlP pincer ligand. We have revealed the reaction mechanism based on the characterization of the reaction intermediate and deuterium-labeling experiments. Notably, this novel catalytic system shows steric-hindrance-dependent chemoselectivity that is distinct from conventional Ni-based catalysts and suggests a new strategy for selective C-O bond activation by heterobimetallic catalysis.
Preparation of branched siloxane
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Page/Page column 10-11, (2010/02/10)
By reacting a branched siloxane compound of formula (2) containing compounds of formula (1) as an impurity with a disiloxane compound of formula (3) in the presence of an acid compound, there is prepared a branched siloxane of formula (2) containing a reduced level of compounds of formula (1).R1?nSi(OSiR2?3)3-n(OR3)R1?nSi(OSiR2?3)4-nR2?3SiOSiR2?3 R1 is a monovalent hydrocarbon group, R2 and R3 are H or monovalent hydrocarbon groups, and n is 0 or 1.
