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1747-57-5

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1747-57-5 Usage

Class

Cyclosiloxane

Structure

A ring consisting of four silicon atoms and eight methyl groups

Common use

Precursor in the synthesis of silicon-containing materials

Applications

Building block for advanced materials, catalyst in organic synthesis, component in electronic devices and coatings

Thermal stability

High

Inertness

High

Resistance to oxidation

High

Utility

Wide-ranging in materials science, chemistry, and engineering

High-temperature environments

Suitable for use due to thermal stability

Protective coating

Valuable due to resistance to oxidation and inertness

Check Digit Verification of cas no

The CAS Registry Mumber 1747-57-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,4 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1747-57:
(6*1)+(5*7)+(4*4)+(3*7)+(2*5)+(1*7)=95
95 % 10 = 5
So 1747-57-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H32Si4/c1-13(2)9-14(3,4)11-16(7,8)12-15(5,6)10-13/h9-12H2,1-8H3

1747-57-5SDS

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 1,1,3,3,5,5,7,7-octamethyl-1,3,5,7-tetrasilocane

1.2 Other means of identification

Product number -
Other names 1,1,3,3,5,5,7,7-Oktamethyl-1,3,5,7-tetrasilacyclooctan

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:1747-57-5 SDS

1747-57-5Downstream Products

1747-57-5Relevant articles and documents

L'electrosynthese, une alternative pour la synthese de polycarbosilanes

Bordeau, M.,Biran, C.,Pons, P.,Leger, M.-P.,Dunogues, J.

, p. C21 - C24 (2007/10/02)

The electrochemical reduction of chloromethyldimethylchlorosilane affords polycarbosilanes in high yields and this route constitutes a competitive route to 1,1,3,3-tetramethyl-1,3-disilacyclobutane formed in 34percent crude yield.The solvent mixture was varied to yield its precursor, Cl(CH2SiMe2)2Cl, in 43percent yield after distillation, while electrosynthesis in the presence of dimethyldichlorosilane provided bis(dimethyl-chlorosilyl)methane, another polycarbosilane precursor, in 60percent yield after distillation.

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