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2-(3,4-EPOXYCYCLOHEXYL) ETHYLMETHYL DIMETHOXYSILANE is a colorless liquid chemical compound with a molecular formula of C10H22O4Si and a molecular weight of 242.37 g/mol. It features a cyclohexyl epoxide group and a silane group, which make it a versatile coupling and crosslinking agent in the formulation of polymers and composites. 2-(3,4-EPOXYCYCLOHEXYL) ETHYLMETHYL DIMETHOXYSILANE is also recognized for its role as a surface treatment agent, enhancing the adhesion of organic coatings on inorganic substrates. Its applications extend to various industries, including electronics, construction, and automotive, where it contributes to material strength and durability. However, due to its flammability and reactivity, careful handling and storage are essential.

97802-57-8

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97802-57-8 Usage

Uses

Used in Adhesives and Sealants Industry:
2-(3,4-EPOXYCYCLOHEXYL) ETHYLMETHYL DIMETHOXYSILANE is used as a coupling agent and crosslinking agent for improving the performance and durability of adhesives and sealants. Its ability to bond with various substrates enhances the adhesion and stability of these products.
Used in Coatings Industry:
In the coatings industry, 2-(3,4-EPOXYCYCLOHEXYL) ETHYLMETHYL DIMETHOXYSILANE is used as a surface treatment agent to improve the adhesion of organic coatings on inorganic substrates, leading to better durability and resistance to environmental factors.
Used in Electronics Industry:
2-(3,4-EPOXYCYCLOHEXYL) ETHYLMETHYL DIMETHOXYSILANE is used in the electronics industry to enhance the strength and durability of materials, contributing to the reliability and longevity of electronic components and devices.
Used in Construction Industry:
In the construction industry, 2-(3,4-EPOXYCYCLOHEXYL) ETHYLMETHYL DIMETHOXYSILANE is utilized for its ability to improve material strength and durability, making it suitable for various construction applications such as concrete additives and protective coatings.
Used in Automotive Industry:
2-(3,4-EPOXYCYCLOHEXYL) ETHYLMETHYL DIMETHOXYSILANE is used in the automotive industry to enhance the performance and durability of materials used in vehicle components, contributing to improved safety, performance, and longevity of the vehicles.

Check Digit Verification of cas no

The CAS Registry Mumber 97802-57-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,8,0 and 2 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 97802-57:
(7*9)+(6*7)+(5*8)+(4*0)+(3*2)+(2*5)+(1*7)=168
168 % 10 = 8
So 97802-57-8 is a valid CAS Registry Number.
InChI:InChI=1/C11H22O3Si/c1-12-15(3,13-2)7-6-9-4-5-10-11(8-9)14-10/h9-11H,4-8H2,1-3H3

97802-57-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name dimethoxy-methyl-[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]silane

1.2 Other means of identification

Product number -
Other names 2-(2-ISO-PROPOXY-PHENYL)-QUINOLINE-4-CARBOXYLIC

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:97802-57-8 SDS

97802-57-8Synthetic route

1,2-Epoxy-4-vinylcyclohexane
106-86-5

1,2-Epoxy-4-vinylcyclohexane

diethoxymethylane
2031-62-1

diethoxymethylane

β-(3,4-epoxycyclohexyl)ethylmethyldimethoxysilane
97802-57-8

β-(3,4-epoxycyclohexyl)ethylmethyldimethoxysilane

Conditions
ConditionsYield
With H2PtCl6; acetic acid In ethanol at 90℃; for 1h;84 %Chromat.

97802-57-8Downstream Products

97802-57-8Relevant academic research and scientific papers

Unexpected silicon group transfer in difunctional alkoxy silanes

Filipkowski, Michelle A.,Petty, Herbert E.,Westmeyer, Mark D.,Schilling Jr., Curtis L.

, p. 15 - 19 (2013/09/06)

During the hydrosilylation reaction of a difunctional silane with allyl glycidyl ether (AGE), two scrambled hydrosilylation products were produced in significant amounts. This scrambling is reaction condition dependent and has been observed in a few other examples. It appears to be the first such alkoxysilane transformation to occur under these conditions, although similar siloxane transformations have been documented. This also introduces a method of preparing certain organofunctional alkyldialkoxysilanes in high purities via hydrosilylation, where the close boiling rearrangement by-products are minimized.

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