54175-55-2

Usage

Uses

Used in Silicone Rubber and Resin Production:
3-(Trimethylsiloxypropyl)dimethylchlorosilane is used as a crosslinking agent for enhancing the strength and durability of silicone rubbers and resins. Its ability to form stable crosslinks improves the overall performance of these materials.
Used in Surface Modification:
3-(Trimethylsiloxypropyl)dimethylchlorosilane is used as a surface modifier to improve the properties of various materials, including glass, metals, and plastics. It can enhance adhesion, wettability, and other surface characteristics, making it suitable for a wide range of applications.
Used in Organosilicon Compound Synthesis:
3-(Trimethylsiloxypropyl)dimethylchlorosilane is utilized in the synthesis of other organosilicon compounds, which have diverse applications in various industries, such as electronics, automotive, and construction.
Used in Adhesive and Sealant Manufacturing:
3-(Trimethylsiloxypropyl)dimethylchlorosilane is used in the production of adhesives and sealants, where its crosslinking properties contribute to the formation of strong bonds and durable seals.

InChI:InChI=1/C8H21ClOSi2/c1-11(2,3)10-7-6-8-12(4,5)9/h6-8H2,1-5H3

Upstream product

• 1066-35-9 dimethylmonochlorosilane 
• 18146-00-4 allyloxytrimethylsilane 

Downstream Products

• 57292-94-1 3-[dimethyl(p-methylphenyl)silyl]-1-propanol 

Relevant academic research and scientific papers

Poly(ferrocenylsilane-block-methacrylates) via Sequential Anionic and Atom Transfer Radical Polymerization

A route to 2-bromoisobutyryl end-functionalized poly(ferrocenyldimethylsilane), allowing essentially quantitative end-capping was discussed. Following the formation of the organometallic block by anionic polymerization, a ruthenium-mediated controlled radical polymerization of methyl methacrylate was employed to grow the second block. Well-defined PFS-b-PMMA block copolymers with low polydispersities and controlled compositions were obtained. The use of atom transfer radical polymerization (ATRP) to form the second block implies that a wide variety of (meth)acrylic and other vinyl monomers can be used, which opens the way to novel hybrid organic-organometallic block copolymers and amphiphilic organometallic block copolymers.

Room-Temperature Gold-Catalysed Arylation of Heteroarenes: Complementarity to Palladium Catalysis

Tailoring of the pre-catalyst, the oxidant and the arylsilane enables the first room-temperature, gold-catalysed, innate C?H arylation of heteroarenes. Regioselectivity is consistently high and, in some cases, distinct from that reported with palladium ca

FUNCTIONALIZED SILANES AND ELECTROLYTE COMPOSITIONS AND ELECTROCHEMICAL DEVICES CONTAINING THEM

Described are compounds of the structure R4-a-Si-(Sp-Y)a-Zb, wherein "a" is integer from 1 to 4; "b" is an integer from 0 to (3 x a); "Z," which is absent when "b "R" or formula (II), wherein each "R" is halogen, C1-6 linear or branched alkyl, alkenyl, or alkynyl or C1-6 linear or branched halo-alkyl, halo-alkenyl, or halo-alkynyl; each "Sp" C1-15 linear or branched alkylenyl or CMS linear or branched halo-alkylenyl; and each "Y" an organic polar group. Also described are electrolyte compositions containing one or more of these compounds.

Immobilization of biomolecules via ruthenium-catalyzed functionalization of the surface of silica with a vinylsilane

A new ruthenium complex catalyzed procedure for the efficient O-silylation of an SiO-H group on the silica surface of glass beads with controlled pores (CPG) using 1-trimethylsiloxy-3-dimethylvinylsilylpropane leading to Si-O-Si bond formation with the evolution of ethylene is described. The formed linker contains alkyl hydroxyl groups which can be reacted with a nucleoside phosphoramidite unit. The CPG support containing alkyl hydroxyl groups is successfully applied in automatic chemical synthesis of DNA fragments.