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17903-53-6

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17903-53-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17903-53-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,0 and 3 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 17903-53:
(7*1)+(6*7)+(5*9)+(4*0)+(3*3)+(2*5)+(1*3)=116
116 % 10 = 6
So 17903-53-6 is a valid CAS Registry Number.

17903-53-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name chloro-diethoxy-phenylsilane

1.2 Other means of identification

Product number -
Other names Phenyldiethoxychlorosilane

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:17903-53-6 SDS

17903-53-6Relevant articles and documents

Some regularities of chlorosilanes etherification

Belyakova,Komarov,Bykovchenko,Ershov,Chernyshev,Storozhenko

experimental part, p. 1650 - 1655 (2011/05/13)

The influence of reagents, solvent polarity, and temperature on the etherification of chlorosilanes ClCH2SiCl3, VinSiCl 3, PrSiCl3, and Ph3SiCl with ethanol was studied. Influence of reaction temperature on the ratio of the synthesized alkoxysilane and related side-product siloxane is revealed. Use of excess alcohol is shown to increase the content of siloxane. Introduction of FeCl 3 does not affect the synthesis. Solvents are shown to influence the reaction rate: the rate constant increases with increasing ε parameter of the solvent. The rate constant of etherification of chlorosilanes with ethanol falls in the series: ClCH2SiCl3 > VinSiCl3 > PrSiCl3. An explanation of the regularities is suggested.

Reaction of Tetraalkoxysilanes with Alkyl(aryl)chlorosilanes

Chernyshev, E. A.,Komalenkova, N. G.,Tagachenkov, A. A.,Bykovchenko, V. G.

, p. 241 - 243 (2007/10/03)

Alkyl(aryl)trichloro- or dialkyl(diaryl)dichlorosilanes react with tetraalkoxysilanes Si(OMe)4, Si(OEt)4, and Si(OBu)4 to give partially etherfied alkyl(aryl)chlorosilanes RSiCl2(OAlk), RSiCl(OAlk)2, and R2SiCl(OAlk).

QUANTITATIVE CHARACTERISTICS OF STEPWISE ETHERIFICATION OF ORGANOCHLOROSILANES

Molchanov, B. V.,Ryzhova, O. G.,Chernyshev, E. A.,Ivanov, V. I.,Kovalenko, V. I.

, p. 1850 - 1852 (2007/10/02)

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