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1065-95-8

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1065-95-8 Usage

General Description

OCTAPHENYLCYCLOTETRASILANE is a chemical compound with the molecular formula C40H32Si4. It is a type of organosilicon compound that consists of a silicon atom bound to four phenyl groups, arranged in a cyclic tetramer structure. OCTAPHENYLCYCLOTETRASILANE has various industrial applications, particularly in the electronics industry, where it is used as a precursor in the production of silicon-based materials such as silicones and silicon carbide. OCTAPHENYLCYCLOTETRASILANE is also used in material science research and as a building block in the synthesis of other organosilicon compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 1065-95-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,6 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1065-95:
(6*1)+(5*0)+(4*6)+(3*5)+(2*9)+(1*5)=68
68 % 10 = 8
So 1065-95-8 is a valid CAS Registry Number.
InChI:InChI=1/C48H40Si4/c1-9-25-41(26-10-1)49(42-27-11-2-12-28-42)50(43-29-13-3-14-30-43,44-31-15-4-16-32-44)52(47-37-21-7-22-38-47,48-39-23-8-24-40-48)51(49,45-33-17-5-18-34-45)46-35-19-6-20-36-46/h1-40H

1065-95-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,1,2,2,3,3,4,4-octakis-phenyltetrasiletane

1.2 Other means of identification

Product number -
Other names Oktaphenyl-cyclotetrasilan

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:1065-95-8 SDS

1065-95-8Related news

Some dichloro compounds derived from OCTAPHENYLCYCLOTETRASILANE (cas 1065-95-8) and decaphenylcyclopentasilane07/24/2019

A study of the preparation of α,ω-dichloropolydiphenylsilanes from octaphenylcyclotetrasilane (I) and decaphenylcyclopentasilane (II) with chlorinating reagents such as 1,1,2,2-tetrachloroethane, phosphorus pentachloride and chlorine is discussed. The study has led to the preparation of compou...detailed

1065-95-8Relevant articles and documents

Gilman et al.

, p. 167,169 (1965)

-

Smith,C.L.,Gooden,R.

, p. 33 - 40 (1974)

-

Thermal Synthesis of Perchlorinated Oligosilanes: A Fresh Look at an Old Reaction

Neumeyer, Felix,Schweizer, Julia I.,Meyer, Lioba,Sturm, Alexander G.,Nadj, Andor,Holthausen, Max C.,Auner, Norbert

, p. 12399 - 12405 (2017)

A combined experimental and theoretical study of the high-temperature reaction of SiCl4 and elemental silicon is presented. The nature and reactivity of the product formed upon rapid cooling of the gaseous reaction mixture is investigated by comparison with the defined model compounds cyclo-Si5Cl10, n-Si5Cl12 and n-Si4Cl10. A DFT assessment provides mechanistic insight into the oligosilane formation. Experimental 29Si NMR investigations, supported by quantum-chemical 29Si NMR calculations, consistently show that the reaction product is composed of discrete molecular perchlorinated oligosilanes. Low-temperature chlorination is an unexpectedly selective means for the transformation of cyclosilanes to acyclic species by endocyclic Si?Si bond cleavage, and we provide a mechanistic rationalization for this observation. In contrast to the raw material, the product obtained after low-temperature chlorination represents an efficient source of neo-Si5Cl12 or the amine-stabilized disilene EtMe2N?SiCl2Si(SiCl3)2 through reaction with aliphatic amines.

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