17865-32-6

Basic information

• Product Name: Cyclohexyldimethoxymethylsilane
• Synonyms: CYCLOHEXYLMETHYLDIMETHOXYSILANE;CYCLOHEXYLDIMETHOXYMETHYLSILANE;DYNASYLAN 9407;METHYL CYCLOHEXYL DIMETHOXY SILANE;CYCLOHEXYLDIMETHOXYMETHYLSILANE, 99+%;Silane,CMDMS;Silane, cyclohexyldimethoxymethyl-;dow corning product z-6187
• CAS NO: 17865-32-6
• Molecular Formula: C₉H₂₀O₂Si
• Molecular Weight: 188.34
• EINECS: 402-140-1
• Product Categories: Dialkoxysilanes;Si (Classes of Silicon Compounds);Silicon Compounds (for Synthesis);Si-O Compounds;Synthetic Organic Chemistry
• Mol File: 17865-32-6.mol

Chemical Properties

• Melting Point: <-72°C
• Boiling Point: 201.2 °C(lit.)
• Flash Point: 165 °F
• Appearance: Colorless, transparent liquid
• Density: 0.94 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.648mmHg at 25°C
• Refractive Index: n20/D 1.439(lit.)
• Storage Temp.: Inert atmosphere,Room Temperature
• Water Solubility: 151-1000000mg/L at 20℃
• Sensitive: Moisture Sensitive
• BRN: 2827648
• CAS DataBase Reference: Cyclohexyldimethoxymethylsilane(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexyldimethoxymethylsilane(17865-32-6)
• EPA Substance Registry System: Cyclohexyldimethoxymethylsilane(17865-32-6)

Safety Data

• Hazard Codes: Xi,N
• Statements: 38-51/53
• Safety Statements: 24-61
• RIDADR: UN 3082 9/PG 3
• WGK Germany: 2
• F: 10-21
• TSCA: Yes
• HazardClass: 9
• PackingGroup: III
• Hazardous Substances Data: 17865-32-6(Hazardous Substances Data)

Usage

Uses

Used in Chemical Research:
Cyclohexyldimethoxymethylsilane is used as a research chemical for its distinctive chemical properties, enabling scientists to explore its potential applications and interactions with other compounds in various chemical reactions and processes.
Used in Material Science:
In the field of material science, Cyclohexyldimethoxymethylsilane is utilized as a precursor or intermediate in the synthesis of advanced materials, such as polymers, coatings, and adhesives, due to its reactive silane group and cyclohexyl moiety.
Used in Pharmaceutical Industry:
Cyclohexyldimethoxymethylsilane is employed as a building block or reagent in the development of pharmaceutical compounds, potentially contributing to the creation of novel drugs with improved therapeutic properties and efficacy.
Used in Nanotechnology:
In nanotechnology, Cyclohexyldimethoxymethylsilane is used as a component in the fabrication of nanostructures and materials, such as nanoparticles, nanowires, and thin films, owing to its ability to form stable and functional coatings on various surfaces.
Used in Surface Modification:
Cyclohexyldimethoxymethylsilane is utilized as a surface modifier to alter the properties of materials, such as improving their hydrophobicity, adhesion, or biocompatibility, which can be beneficial in various industries, including electronics, textiles, and biomedical applications.

InChI:InChI=1/C9H20O2Si/c1-10-12(3,11-2)9-7-5-4-6-8-9/h9H,4-8H2,1-3H3

Upstream product

• 1185-55-3 Methyltrimethoxysilan 
• 931-51-1 cyclohexylmagnesiumchloride 
• 108-85-0 1-bromocyclohexane 
• 1634-04-4 tert-butyl methyl ether 
• 5578-42-7 dichlorocyclohexylmethylsilane 
• 16881-77-9 (dimethoxy)methylsilane 
• 110-83-8 cyclohexene 

Downstream Products

• 18295-72-2 cyclohexyl-methyl-silanediol 
• 2096-99-3 cyclohexyl(methyl)silane 

Relevant articles and documents

METHOD FOR PRODUCING ORGANOSILICON COMPOUND HAVING CYCLIC ALKYL GROUP

PROBLEM TO BE SOLVED: To provide a method for producing an organosilicon compound that can efficiently produce an organosilicon compound, particularly an organic silicon compound having a cyclic alkyl group. SOLUTION: A method according to the present inv

METHOD OF PRODUCING A HYDROLYZABLE SILICON-CONTAINING COMPOUND

The present invention provides a safe, inexpensive, and high yield means of producing a hydrolyzable silicon-containing compound, e.g., an organooxysilane and the like. A compound (A) represented by the general formula R1-O-R2 wherein R1 represents a C4-30, substituted or unsubstituted, tertiary alkyl group or aralkyl group and R2 represents a C1-30, substituted or unsubstituted, monovalent hydrocarbyl group or acyl group, is reacted in the presence of a Lewis acid catalyst with a halosilane (B) represented by the general formula R3mSiX4-m wherein R3 represents the hydrogen atom or a C1-30 substituted or unsubstituted monovalent hydrocarbyl group, X is independently bromine or chlorine, and m represents an integer from 0 to 3.

Practical conversion of chlorosilanes into alkoxysilanes without generating HCl

Alcohol-free: A versatile, efficient, and practical synthesis of alkoxysilanes without generation of HCl involves the reaction of chlorosilanes with unsymmetrical ethers in the presence of a Lewis acid (see scheme). The reaction proceeds through selective cleavage of C-O bonds and is superior to conventional processes. Industrially feasible reagents are used and only one by-product results. Copyright