17865-54-2

Basic information

• Product Name: CYCLOHEXYLTRIMETHOXYSILANE
• Synonyms: CYCLOHEXYLTRIMETHOXYSILANE;Cyclohexane,(trimethoxysilyl)-
• CAS NO: 17865-54-2
• Molecular Formula: C₉H₂₀O₃Si
• Molecular Weight: 204.34
• Product Categories: Si (Classes of Silicon Compounds);Si-O Compounds;Trialkoxysilanes
• Mol File: 17865-54-2.mol
• Article Data: 5

Chemical Properties

• Melting Point: <0°C
• Boiling Point: 207 °C
• Flash Point: >60°C
• Appearance: /
• Density: 1.00
• Vapor Pressure: 0.199mmHg at 25°C
• Refractive Index: 1.4310-1.4350
• Storage Temp.: Inert atmosphere,Room Temperature
• CAS DataBase Reference: CYCLOHEXYLTRIMETHOXYSILANE(CAS DataBase Reference)
• NIST Chemistry Reference: CYCLOHEXYLTRIMETHOXYSILANE(17865-54-2)
• EPA Substance Registry System: CYCLOHEXYLTRIMETHOXYSILANE(17865-54-2)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• TSCA: No
• Hazardous Substances Data: 17865-54-2(Hazardous Substances Data)

Usage

General Description

CYCLOHEXYLTRIMETHOXYSILANE is a chemical compound with the formula C9H22O3Si. It is a clear, colorless liquid that is commonly used as a crosslinking agent in the production of silicone polymers and resins. It is also utilized as a surface modifier to improve adhesion and durability of coatings, adhesives, and sealants. CYCLOHEXYLTRIMETHOXYSILANE is known for its ability to enhance weatherability and moisture resistance of materials, making it a valuable component in various industrial and commercial applications. Additionally, it is also used in the synthesis of organic compounds and as a coupling agent in the formulation of composite materials. Overall, CYCLOHEXYLTRIMETHOXYSILANE plays a crucial role in the development of advanced materials with improved performance and durability.

InChI:InChI=1/C9H20O3Si/c1-10-13(11-2,12-3)9-7-5-4-6-8-9/h9H,4-8H2,1-3H3

Upstream product

• 2487-90-3 trimethoxysilane 
• 110-83-8 cyclohexene 
• 108-85-0 1-bromocyclohexane 
• 681-84-5 tetramethylorthosilicate 
• 67-56-1 methanol 
• 98-12-4 cyclohexyltrichlorosilane 

Downstream Products

• 18162-96-4 cyclohexylsilane 
• 15493-30-8 dicyclohexylsilane 
• 1629-47-6 tricyclohexylsilane 

Relevant articles and documents

Stereocontrol in Nucleophilic Substitution Reactions at Silicon: The Role of Permutation in Generating Silicon-Centered Chirality

Intramolecular isomerization in pentacoordinate compounds can play an essential role for the adjustment of defined stereochemical information. Here, we present a conclusive mechanism of a stereocontrolled reaction on chiral dimethoxysilanes that opens new aspects in understanding the origin of creating silicon-centered chirality during a nucleophilic substitution process. By combining experimental, structural, and quantum chemical methods, we were able to disclose an interconversion process, based on consecutive Berry-type motions, as the most plausible mechanism for describing the stereochemical outcome in suchlike substitution reactions.

Preparation of diisopropylammonium bis(catecholato)cyclohexylsilicate

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A method for the preparation of a cycloalkyl silane compound

Cycloalkyl silane compound such as cyclohexyl methyl di-chlorosilane can be efficiently prepared by the photochemically induced hydrosilylation reaction. For example, an equimolar mix-ture of cyclohexene and methyl dichlorosilane and admixture of a catalytic amount of a platinum compound, e.g., chloroplatinic acid, is irradiated at a temperature up to 70 °C with ultraviolet light so that the hydrosilylation reaction takes place and proceeds almost to completeness without deactivation of the platinum catalyst to give the desired product in a yield of 90% or even higher.