106773-87-9

Basic information

• Product Name: (chloromethyl)(4-ethoxyphenyl)dimethylsilane
• CAS NO: 106773-87-9
• Molecular Formula: C₁₁H₁₇ClOSi
• Molecular Weight: 228.7906
• Mol File: 106773-87-9.mol

Chemical Properties

• Boiling Point: 284.2°C at 760 mmHg
• Flash Point: 105.1°C
• Density: 1.01g/cm³
• Vapor Pressure: 0.00519mmHg at 25°C
• Refractive Index: 1.49
• CAS DataBase Reference: (chloromethyl)(4-ethoxyphenyl)dimethylsilane(CAS DataBase Reference)
• NIST Chemistry Reference: (chloromethyl)(4-ethoxyphenyl)dimethylsilane(106773-87-9)
• EPA Substance Registry System: (chloromethyl)(4-ethoxyphenyl)dimethylsilane(106773-87-9)

Safety Data

• Hazardous Substances Data: 106773-87-9(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
(Chloromethyl)(4-ethoxyphenyl)dimethylsilane is utilized as a reagent in organic synthesis, where it contributes to the formation of various complex organic molecules. Its unique structure allows for specific reactions and functional group transformations that are beneficial in creating a diverse array of chemical products.
Used in Silane-based Material Production:
(chloromethyl)(4-ethoxyphenyl)dimethylsilane is also employed in the production of various silane-based materials. These materials have a broad spectrum of applications, including as coupling agents, adhesives, and components in the manufacturing of electronic devices.
Used in Organic Electronics:
(Chloromethyl)(4-ethoxyphenyl)dimethylsilane has been studied for its potential applications in the field of organic electronics. Its properties make it a candidate for use in the development of electronic components, such as semiconductors and insulators, that can be integrated into organic electronic devices.
Used as a Precursor for Functionalized Silsesquioxanes:
Additionally, the compound serves as a precursor for functionalized silsesquioxanes, which are important materials in the field of materials science. These silsesquioxanes have applications in areas such as coatings, adhesives, and sealants, as well as in the electronics and automotive industries due to their thermal stability and unique physical properties.

Upstream product

• 1719-57-9 Chloro(chloromethyl)dimethylsilane 
• 588-96-5 4-bromoethoxybenzene 
• 119307-44-7 chloromethyl-dimethyl-(4-fluorobenzyl)silane 

Downstream Products

• 99503-07-8 2-(4-ethoxyphenyl)-2-methyl-2-silapropanol 

Relevant articles and documents

Fungicidal (1H-1,2,4-triazolyl)disilaalkanes

This invention relates to (1H-1,2,4-triazolyl)disilaalkanes as represented by formula I, their preparation, and their use in controlling fungus diseases of living plants. STR1 wherein R1, R2, R3, R4, and R5 can be independently lower alkyl, vinyl, allyl, benzyl, or substituted phenyl such as para-fluorophenyl, para-chlorophenyl, para-enthoxyphenyl, and biphenyl.

Substituted phenyltrialkylsilane insecticides

Compounds of the formula STR1 in which Ar is substituted or unsubstituted phenyl, pyridinyl, furanyl, naphthyl, thienyl, or thiazolyl; R is a (C1-4) alkyl; W is oxygen or methylene; and Ph is substituted or unsubstituted phenoxyphenyl, benzylph

Ether compounds carrying substituted silyl group

A compound of the formula: STR1 wherein R1 and R2 are each phenyl optionally substituted by one selected from the group consisting of C1 -C5 alkyl, C1 -C5 alkoxy, C1 -C5/su

Substituted phenyltrialkylsilane insecticides

Compounds containing a dimethylsilane core and a phenoxybenzyl substituent are found to exhibit pyrethroid-like activity toward insects with low toxicity to fish.