69983-36-4

Usage

Uses

Used in Silicone Polymer Production:
Bis(4-methoxyphenyl)dimethylsilane, 97% serves as a crosslinking agent, enhancing the structural integrity and performance of silicone polymers. Its reactivity and stability contribute to the formation of robust polymer networks, improving the overall quality and durability of the end products.
Used in Material Protection:
As a protective agent, Bis(4-methoxyphenyl)dimethylsilane, 97% is utilized to shield various materials from environmental factors such as moisture, UV radiation, and chemical exposure. Its ability to form stable bonds with different surfaces ensures long-lasting protection and preservation of material properties.
Used in Coatings Industry:
Bis(4-methoxyphenyl)dimethylsilane, 97% is employed as a component in the development of high-performance coatings. Its crosslinking capabilities contribute to the creation of coatings with enhanced durability, resistance to environmental factors, and improved adhesion to various substrates.
Used in Adhesives Industry:
In the adhesives industry, Bis(4-methoxyphenyl)dimethylsilane, 97% is used to improve the bonding strength and stability of adhesive formulations. Its reactivity allows for the formation of strong bonds between different materials, ensuring reliable and long-lasting adhesion.
Used in Electronic Industry:
Bis(4-methoxyphenyl)dimethylsilane, 97% is utilized in the electronic industry as a component in the manufacturing of electronic devices and components. Its protective properties help safeguard sensitive electronic components from environmental factors, thereby enhancing their performance and longevity.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, Bis(4-methoxyphenyl)dimethylsilane, 97% may be employed as a component in drug delivery systems or as a protective agent for sensitive pharmaceutical compounds. Its stability and reactivity can contribute to the development of more effective and reliable drug formulations.

InChI:InChI=1/C16H20O2Si/c1-17-13-5-9-15(10-6-13)19(3,4)16-11-7-14(18-2)8-12-16/h5-12H,1-4H3

Upstream product

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Relevant academic research and scientific papers

METHOD FOR PRODUCING ARYLSILANE COMPOUND CONTAINING HALOSILANE COMPOUND AS RAW MATERIAL

PROBLEM TO BE SOLVED: To provide a method for producing an arylsilane compound with low production cost. SOLUTION: A method for producing an arylsilane compound includes a reaction step for the cross-coupling reaction of a halosilane compound represented by general formula (A-1), (A-2), or (A-3) and an arylboronic acid pinacol ester in the presence of a nickel catalyst, a Lewis acid catalyst, and an organic base (R independently represent an aromatic hydrocarbon group, a heteroaromatic ring group, or a C1-20 hydrocarbon group; X independently represent a halogeno group or a trifluoromethanesulfonyloxy group). SELECTED DRAWING: None COPYRIGHT: (C)2020,JPOandINPIT

Modular diphosphine ligands based on bisphenol A backbones

A straightforward two-step synthesis is used to obtain new phosphorus-containing ligands based on readily available bisphenol A type backbones. Five diphosphine ligands have been prepared in good yields. An X-ray crystallographic study is presented for li

New Diphosphane Ligands Based on Bisphenol A Backbones - Synthesis and Coordination Chemistry

A series of easily accessible diphosphane compounds 1-4, based on bisphenol A derived backbones, has been prepared. A straightforward two-step synthetic route has been employed to obtain these new ligands in good yields from cheap starting materials. Mole

Synthesis of biaryls by intramolecular radical aryl migration from silicon to carbon

(equation presented) A new method for the preparation of biaryls via intramolecular 1,5 aryl migration reaction from silicon in silyl ethers to aryl radicals is presented. Various readily available diphenylsilyl ethers can be used as substrates in this reaction. Functionalized aryl groups can also be transferred. The analogous 1,4 aryl migration reaction is less efficient.

Transmission of electronic effects via a SiMe2 spacer in 4-mono- and 4,4'-disubstituted diphenyldimethylsilanes: 29Si and 13C NMR spectroscopy and PM3 semi-empirical calculations

Some 29Si and 13C NMR studies were performed of series of 4-substituted phenyltrimethylsilanes and 4-substituted and 4,4'-disubstituted diphenyldimethylsilanes.Within each series linear relationships are found between the chemical shifts and (a) the Hammett substituent constants ?p and (b) the PM3-calculated total atomic charges.It is inferred that the SiMe2 ?-type spacer weakly mediates substituent effects in the ground state via a bond polarization mechanism.A comparison with available data for 4-substituted and 4,4'-disubstituted diphenylmethanes shows that the SiMe2 group is a better transmitter of electronic effects that the CH2 group. Keywords: Silicon; 29Si NMR; 13C NMR; Substituent effects; MO calculations