93804-29-6

Usage

Uses

Used in Surface Modification Industry:
DIMETHYLMETHOXY-N-OCTYLSILANE is used as a functionalizing agent for partially oxidized porous silicon. It serves to enhance the surface properties of porous silicon by introducing silane groups, which can improve the material's stability, biocompatibility, and other functional characteristics. This application is particularly relevant in the development of advanced materials for various industries, such as electronics, pharmaceuticals, and biomedical engineering, where the modification of surfaces can lead to improved performance and novel functionalities.

InChI:InChI=1/C11H26OSi/c1-5-6-7-8-9-10-11-13(3,4)12-2/h5-11H2,1-4H3

Upstream product

• 67-56-1 methanol 
• 226225-89-4 dimethyl(1-octyl)(2-pyridyl)silane 
• 111-83-1 1-bromo-octane 
• 3429-76-3 trimethyl-octyl-silane 
• 81272-80-2 allyldimethyloctylsilane 

Downstream Products

• 40934-68-7 octyldimethylhydrosilane 
• 111-87-5 octanol 

Relevant academic research and scientific papers

Utilization of a Trimethylsilyl Group as a Synthetic Equivalent of a Hydroxyl Group via Chemoselective C(sp3)-H Borylation at the Methyl Group on Silicon

A conversion of trimethylsilylalkanes into the corresponding alcohols is established based on an iridium-catalyzed, chemoselective C(sp3)-H borylation of the methyl group on silicon. The (borylmethyl)silyl group formed by C(sp3)-H borylation is treated with H2O2/NaOH, and the resulting (hydroxymethyl)silyl group is converted into a hydroxyl group by Brook rearrangement, followed by oxidation of the resulting methoxysilyl group under Tamao conditions. An alternative route proceeding through the formylsilyl group formed from a (hydroxymethyl)silyl group by Swern oxidation is also established. The method is applicable to substituted trimethylsilylcycloalkanes and 1,1-dimethyl-1-silacyclopentane for conversion into the corresponding stereodefined cycloalkyl alcohols and 1,4-butanediol.

Method for Attachment of Silicon-Containing Compounds to a Surface and for Synthesis of Hypervalent Silicon-Compounds

A method for inducing a hypervalent state within silicon-containing compounds by which they can be chemically attached to a surface or substrate and/or organized onto a surface of a substrate. The compounds when attached to or organized on the surface may have different physical and/or chemical properties compared to the starting materials.

ELECTROCHEMICAL OXIDATION OF ORGANOSILICON COMPOUNDS I. OXIDATIVE CLEAVAGE OF CARBON-SILICON BOND IN ALLYLSILANES AND BENZYLSILANES

Electrochemical oxidation of allylsilanes and benzylsilanes in the presence of alcohol, carboxylic acid, or water resulted in cleavage of the carbon-silicon bond and formation of the corresponding ether, ester, or alcohol, respectively.