28229-56-3

Usage

Uses

Used in Materials Science:
3-Phenoxypropylmethyldichlorosilane is used as a precursor in the synthesis of various materials for applications in materials science. Its unique structure allows for the creation of new materials with tailored properties, such as improved thermal stability or enhanced chemical resistance.
Used in Organic Chemistry:
In the field of organic chemistry, 3-Phenoxypropylmethyldichlorosilane is used as a reagent or intermediate in the synthesis of complex organic molecules. Its versatility in reactions makes it a valuable tool for the development of new compounds with potential applications in pharmaceuticals, agrochemicals, or other industries.
Used in Surface Modification:
3-Phenoxypropylmethyldichlorosilane is used as a coupling agent for surface modification in various industries. Its ability to form covalent bonds with different surfaces allows for the improvement of adhesion, durability, or other properties of materials, making it suitable for applications in coatings, adhesives, or composite materials.
Used in Nanotechnology:
In nanotechnology, 3-Phenoxypropylmethyldichlorosilane is used as a functionalizing agent for the modification of nanoparticles. This enables the tuning of their surface properties, such as hydrophilicity or biocompatibility, which can be crucial for their application in drug delivery, sensing, or other nanoscale systems.

InChI:InChI=1/C10H14Cl2OSi/c1-14(11,12)9-5-8-13-10-6-3-2-4-7-10/h2-4,6-7H,5,8-9H2,1H3

Upstream product

• 75-54-7 Dichloromethylsilane 
• 1746-13-0 allyl phenyl ether 

Downstream Products

• 7787-93-1 dichloro(3-chloropropyl)methylsilane 
• 28229-63-2 Methyl(γ-chloropropyl)phenoxychlorosilan 

Relevant academic research and scientific papers

Effect of catalysts on the reaction of allyl esters with hydrosilanes

The reaction of hydrosilylation of allyl esters XOCH 2CH=CH 2 (X = MeCO, CF 3CO, C 3F 7CO) and PhOCH 2CH=CH 2 with hydrosilanes HSiY 3 (Y = Cl, OEt) in the presence of the Speier catalyst, the Speier catalyst with additives, and of various nickel complexes was studied. The catalytic hydrosilylation reaction in the presence of the Speier catalyst is accompanied by the reduction. Additives to the Speier catalyst (vinyltriethoxysilane and some ethers) allow to suppress considerably the reduction reaction. In the presence of the studied nickel complexes mainly reduction and isomerization reactions occurred. The best nickel catalysts of hydrosilylation were the mixtures of NiCl 2 or Ni(acac) 2 with phosphine oxides. In contrast to allyl esters, the hydrosilylation of simple olefins proceeds easier, the content of the product of hydrosilylation in the reaction mixture reaches 94.3%. Pleiades Publishing, Ltd., 2010.

Polysilanes Bearing a Phenoxypropyl Side Chain

A series of polysilanes bearing a 3-phenoxypropyl side chain was prepared applying the Wurtz coupling reaction of dichlorosilanes. All prepared polymers ([R-Si(CH2)3OPh]n, R = Me, Pent, Hex, Hept, (CH2)3/s

Catalytic activity of bis(dialkylamino)carbenium salts in hydrosilylation reactions

Bis(dialkylamino)carbenium salts {[(Me2N)2CCl]+}2MCl4 2- (M = Ni, Pd) and {[Me2NC(X)NR2]+}2PtCl62- (R = Me, All; X = H, Cl, Me) are efficient catalysts for hydrosilylation of allyl phenyl ether, triallylamine, allyl chloride, allylamine, and 1-octene with various hydrosilanes. The catalytic activity is dependent on the salt composition and the nature of the metal M, the saturated compound, and the hydrosilane used. The catalysts used are usually insoluble in the reaction mixture, active, and stable. In some cases, carbenium salts are more selective than Speier's catalyst. Novel catalysts, silica-immobilized dialkylaminocarbenium salts, have been prepared. The kinetics of the reaction have been considered.