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18171-15-8

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18171-15-8 Usage

General Description

(3-Chloropropoxy)trimethylsilane is a chemical compound commonly used as a coupling agent and surface modifier in the production of various materials and products. It is a colorless liquid that is highly flammable and reactive with water, producing flammable hydrogen gas. (3-Chloropropoxy)trimethylsilane is primarily used in the synthesis of organic and inorganic materials, as well as in the modification of surfaces to improve adhesion and compatibility with other materials. Its unique chemical structure allows it to bond with both organic and inorganic surfaces, making it a versatile and valuable chemical in various industrial applications. However, due to its flammability and reactivity, proper precautions must be taken when handling and using (3-Chloropropoxy)trimethylsilane to ensure safety and prevent accidents.

Check Digit Verification of cas no

The CAS Registry Mumber 18171-15-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,1,7 and 1 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 18171-15:
(7*1)+(6*8)+(5*1)+(4*7)+(3*1)+(2*1)+(1*5)=98
98 % 10 = 8
So 18171-15-8 is a valid CAS Registry Number.
InChI:InChI=1/C6H15ClOSi/c1-9(2,3)8-6-4-5-7/h4-6H2,1-3H3

18171-15-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (3-chloropropoxy)trimethylsilane

1.2 Other means of identification

Product number -
Other names me3Si(On-pr-3-Cl)

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:18171-15-8 SDS

18171-15-8Relevant articles and documents

Salt-free preparation of trimethylsilyl ethers by B(C6F 5)3-catalyzed transfer silylation by using a Me 3SiH surrogate

Simonneau, Antoine,Friebel, Jonas,Oestreich, Martin

supporting information, p. 2077 - 2083 (2014/04/17)

An unprecedented transfer silylation of alcohols catalyzed by the strong Lewis acid B(C6F5)3 is described. Gaseous Me3SiH is released in situ by B(C6F5) 3-catalyzed decomposition of 3-trimethylsilylcyclohexa-1,4-diene and subsequently reacts with an alcohol in a dehydrogenative Si-O coupling promoted by the same boron catalyst. Benzene and dihydrogen are formed during the reaction, but no salt waste is. This expedient protocol is applicable to several silicon groups, and the preparation of trimethylsilyl ethers presented here is potentially useful for alcohol derivatization prior to GLC analysis. Copyright

Facile method for trimethylsilylation of alcohols using hexamethyldisilazane and ammonium thiocyanate under neutral conditions

Jadhav, Vrushali H.,Kumar, K. S. Ajish,Chaudhari, Vinod D.,Dhavale, Dilip D.

, p. 1363 - 1370 (2008/02/01)

A highly efficient method for trimethylsilylation of primary, secondary, tertiary, allylic, and a variety of sugar-derived alcohols using hexamethyldisilazane in the presence of a catalytic amount of ammonium thiocyanate under neutral conditions is reported. Copyright Taylor & Francis Group, LLC.

Process of preparing trimethylsilyloxy functionalized alkyllithium compounds

-

, (2008/06/13)

A process for producing compounds of the formula (CH3)3 SiORLi where in R is selected from alkyl groups containing 2 to 10 carbon atoms and aryl groups containing 6 to 10 carbon atoms by reacting, in an inert atmosphere, in a hydrocarbon solvent, a haloalcohol of the formula HORX wherein R is selected from alkyl groups containing 2 to 10 carbon atoms and aryl groups containing 6 to 10 carbon atoms and X is selected from chlorine or bromine, is reacted with hexamethyldisilazane at a temperature between 20° C. and the reflux temmperature of the solvent after which the resulting product, a trimethylsilyloxyalkylhalide compound, is reacted at a temperature between 50° and 160° C., with powdered lithium metal to produce the (CH3)3 SiORLi compound.

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