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Trimethyl[(1-(trichloromethyl)cyclohexyl)oxy]silane is a complex organic compound with the chemical formula C10H19Cl3O2Si. It is a colorless liquid at room temperature and is soluble in organic solvents. trimethyl[(1-(trichloromethyl)cyclohexyl)oxy]silane is primarily used as a coupling agent in the field of materials science, particularly in the production of composite materials. It functions by forming a covalent bond between the inorganic material (such as glass or ceramic) and the organic polymer matrix, thereby improving the adhesion and mechanical properties of the composite. The trichloromethyl group in the molecule provides a reactive site for bonding with the inorganic material, while the silane group allows for compatibility with the organic polymer. Due to its reactivity and potential health and environmental risks, it is important to handle trimethyl[(1-(trichloromethyl)cyclohexyl)oxy]silane with care, following appropriate safety protocols.

85695-30-3

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85695-30-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85695-30-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,6,9 and 5 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 85695-30:
(7*8)+(6*5)+(5*6)+(4*9)+(3*5)+(2*3)+(1*0)=173
173 % 10 = 3
So 85695-30-3 is a valid CAS Registry Number.

85695-30-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name trimethyl[(1-(trichloromethyl)cyclohexyl)oxy]silane

1.2 Other means of identification

Product number -
Other names -

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:85695-30-3 SDS

85695-30-3Relevant academic research and scientific papers

Process for preparing (2,2,2-trihalo-1, 1-dihydrocarbyl-ethoxy) trihydrocarbylsilanes

-

, (2008/06/13)

A process for forming trihalomethylsiloxanes by contacting a trihalosilane with a carbonyl in the presence of the fluoride ion. These compounds are used to form α-substituted acid chlorides.

TRICHLOROMETHYL ANION CHEMISTRY FROM TRIMETHYLSILYL TRICHLOROACETATE

Jesus, Miguel A. de,Prieto, J. Antonio,Valle, Luis del,Larson, Gerald L.

, p. 1047 - 1052 (2007/10/02)

The reaction of trimethylsilyl trichloroacetate with aldehydes and ketones in the presence of fluoride ion gives the trichloromethyl adducts.With potassium fluoride the reaction with cyclohexenone and crotonaldehyde results in clear 1,2 addition.

TRIMETHYLSILYL TRICHLOROACETATE: A NEW REAGENT FOR SALT-FREE SILYLATIONS

Renga, James M.,Pen-Chung, Wang

, p. 1175 - 1178 (2007/10/02)

Trimethylsylil trichloroacetate (1) is a convenient reagent for the silylation of phenols, carboxylic acids, mercaptans, amides, acetylenes, and β-keto esters, while the reaction of 1 with aldehydes and ketones affords silylated trichloromethyl carbinols (5).

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