55153-99-6

Basic information

• Product Name: 4-METHOXYPHENYL DIMETHYLVINYL SILANE
• Synonyms: VINYL(P-METHOXYPHENYL)DIMETHYLSILANE;4-METHOXYPHENYL DIMETHYLVINYL SILANE;Dimethyl(4-methoxyphenyl)(vinyl)silane;4-Methoxyphenyl Vinyl Dimethylsilane
• CAS NO: 55153-99-6
• Molecular Formula: C11H16OSi
• Molecular Weight: 192.33
• Mol File: 55153-99-6.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 4-METHOXYPHENYL DIMETHYLVINYL SILANE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-METHOXYPHENYL DIMETHYLVINYL SILANE(55153-99-6)
• EPA Substance Registry System: 4-METHOXYPHENYL DIMETHYLVINYL SILANE(55153-99-6)

Safety Data

• TSCA: No
• Hazardous Substances Data: 55153-99-6(Hazardous Substances Data)

Usage

General Description

4-Methoxyphenyl dimethylvinyl silane is a chemical compound with the molecular formula C11H16O2Si. It is a silane coupling agent, commonly used as a surface modifier in polymers and composites to enhance adhesion and improve overall performance. This chemical is also utilized in the formulation of adhesives, sealants, and coatings due to its ability to effectively bond organic materials to inorganic surfaces. Additionally, it has potential applications in the electronics industry as a component in electronic packaging materials and as a precursor for the synthesis of novel organic-inorganic hybrid materials. 4-Methoxyphenyl dimethylvinyl silane is a colorless liquid with a faint odor, and it should be handled and stored with appropriate care due to its flammability and potential hazards.

InChI:InChI=1/C11H16OSi/c1-5-13(3,4)11-8-6-10(12-2)7-9-11/h5-9H,1H2,2-4H3

Upstream product

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Relevant articles and documents

Cross-Electrophile C(sp2)?Si Coupling of Vinyl Chlorosilanes

The cross-electrophile coupling has become a powerful tool for C?C bond formation, but its potential for forging the C?Si bond remains unexplored. Here we report a cross-electrophile Csp2-Si coupling reaction of vinyl/aryl electrophiles with vinyl chlorosilanes. This new protocol offers an approach for facile and precise synthesis of organosilanes with high molecular diversity and complexity from readily available materials. The reaction proceeds under mild and non-basic conditions, demonstrating a high step economy, broad substrate scope, wide functionality tolerance, and easy scalability. The synthetic utility of the method is shown by its efficient accessing of silicon bioisosteres, the design of new BCB-monomers, and studies on the Hiyama cross-coupling of vinylsilane products.

Sequential Synthesis of Organosilicon-Linked 2-Methoxypyridines by Non-Cryogenic ortho-Metallation Using the nBu2TMPMg·Li Reagent and Hydrosilylation

The non-cryogenic synthesis of 5/6- and/or 3-silyl-functionalised 2-methoxypyridines by a 5-Br/Mg exchange process using nBu2iPrMg Li and LiCl and involving C-3 metallation using a novel nBu2TMPMg Li reagent is described. Furthermore, the usefulness of nBu2TMPMg Li in the functionalisation of 2-methoxypyridine at the 3-position with a wide range of electrophiles was successfully tested. The above achievements have allowed the construction of organosilicon-linked 2-methoxypyridines composed of two, three and four rings by the hydrosilylation of 5- and/or 3-SiH(or alkenyl) derivatives using the hitherto rarely applied [Pt(cod)Me2] catalyst. Additionally, the synthesis of a one-chain oligomer consisting of eight 2-methoxypyridines obtained by the hydrosilylation/polymerisation approach, followed by protodesilylation of the SiHMe2 group was also achieved by manipulating the amount of catalyst in the reactions.