1825-74-7

Usage

Uses

Used in Silicone Polymer Synthesis:
Dichloromethoxymethylsilane is used as a precursor for the synthesis of silicone polymers, contributing to the formation of polymers with unique properties such as heat resistance, flexibility, and biocompatibility.
Used in Silicone Rubber and Resin Production:
As a crosslinking agent, dichloromethoxymethylsilane is utilized in the production of silicone rubbers and resins, enhancing their mechanical strength and durability.
Used in Organic Synthesis:
Dichloromethoxymethylsilane is employed as a reagent in organic synthesis, particularly for the preparation of silyl ethers and silyl enol ethers, which are important intermediates in various chemical reactions.
Used in Surface Modification for Biotechnology and Pharmaceuticals:
dichloromethoxymethylsilane serves as a coupling agent in the modification of surfaces, which is crucial for improving the performance of materials in biotechnology and pharmaceutical applications, such as enhancing biocompatibility and stability.
Used in Manufacturing Protective Coatings, Adhesives, and Sealants:
Dichloromethoxymethylsilane is used in the production of protective coatings, adhesives, and sealants, providing properties like adhesion, flexibility, and resistance to environmental factors.
Used in Electronics Industry:
In the electronics industry, dichloromethoxymethylsilane is employed for the production of encapsulants and insulating materials, ensuring the protection and reliable operation of electronic components.

InChI:InChI=1/C2H6Cl2OSi/c1-5-6(2,3)4/h1-2H3

Upstream product

• 67-56-1 methanol 
• 75-79-6 Methyltrichlorosilane 
• 5602-96-0 methyl p-tolylcarbamate 

Downstream Products

• 64451-39-4 Methyl(methoxy)bis(phenylthio)silan 

Relevant academic research and scientific papers

Technology of synthesis of a bis(diethylamino)methoxymethylsilane

The invention relates to a technology of synthesis of a bis(diethylamino)methoxymethylsilane product and belongs to the technical field of fine chemical engineering. The technology comprises that an insufficient amount of methanol is added into a methyltr

Production processes for triorganomonoalkoxysilanes and triorganomonochlorosilanes

A silane containing a bulky hydrocarbon group or groups R therein and having the formula (III) [in-line-formulae]R3-(x+y)(R1)x(R2)ySi(OR3) [/in-line-formulae] can be produced by reacting a silane of the formula (I) [in-line-formulae](R1)x(R2) ySiCl3-(x+y)(OR3) [/in-line-formulae] with a Grignard reagent of the formula (II) [in-line-formulae]RMgX [/in-line-formulae] Further, a tri-organo-chlorosilane of the formula (XIIa) [in-line-formulae](R1)(R2)(R3)SiCl [/in-line-formulae] can be produced by reacting a tri-organo-silane of the formula (XIa) [in-line-formulae](R1)(R2)(R3)SiZ1 [/in-line-formulae] with hydrochloric acid. Furthermore, a tri-organo-monoalkoxysilane of the formula (XXIII) [in-line-formulae]R3-(x+y)(R1)x(R2)ySi(OR3) [/in-line-formulae] can be produced when a silane of the formula (XXI) [in-line-formulae](R1)x(R2)ySiCl4-(x+y) [/in-line-formulae] is reacted with a Grignard reagent of the formula (XXII) [in-line-formulae]RMgX [/in-line-formulae] with addition of and reaction with an alcohol or an epoxy compound during the reaction.

Multilevel selectivity in the mild and high-yielding chlorosilane- induced cleavage of carbamates to isocyanates

The silane-induced cleavage of a series of N-p-tolylcarbamates and N- phenethylcarbamates to isocyanates has been investigated as a function of chlorosilane, carbamate substituent, and reaction conditions. Reaction yields were determined from the isolated ureas, which were formed by trapping the corresponding isocyanates with isobutylamine. Under room-temperature conditions, multilevel selectivity in carbamate activation has been demonstrated. This selectivity together with the generality of the methodology enhances the utility of carbamates as synthetic intermediates and protecting groups. To demonstrate the effectiveness of this selectivity, a series of biscarbamates were selectively monoactivated to isocyanates in excellent yields.