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Disilane, 1,1,2,2-tetramethyl-1,2-bis(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20156-42-7

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20156-42-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20156-42-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,1,5 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 20156-42:
(7*2)+(6*0)+(5*1)+(4*5)+(3*6)+(2*4)+(1*2)=67
67 % 10 = 7
So 20156-42-7 is a valid CAS Registry Number.

20156-42-7SDS

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 BnMe2Si-SiMe2Bn

1.2 Other means of identification

Product number -
Other names 1,1,2,2-tetramethyl-1,2-dibenzyldisilane

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:20156-42-7 SDS

20156-42-7Relevant academic research and scientific papers

Disilane and preparation method thereof

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Paragraph 0046-0049, (2020/01/25)

The invention discloses disilane and a preparation method thereof. The preparation method of disilane includes: subjecting a uniformly mixed reaction system containing tertiary hydrosilane and a catalyst to dehydrogenation reaction at a temperature ranging from -10DEG C to 120DEG C to obtain disilane, wherein the catalyst comprises a silver salt. The invention also discloses the disilane preparedby the method. The method for preparation of the disilane by catalyzing tertiary silane dehydrogenation with the silver salt adopts the silver salt to activate the Si-H bond in the silane so as to realize construction of disilane. Therefore, the invention provides an efficient and simple method for preparation of the compound, and the application prospect is wide.

Method for continuously preparing disilane compounds by micro-reaction device

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Paragraph 0025; 0026; 0039; 0040, (2018/05/16)

The invention discloses a method for continuously preparing disilane compounds by a micro-reaction device. The method comprises the following steps: (1) a solution A is prepared from organosilane by dissolving in a first organic solvent, or is organosilane; (2) a solution B is prepared from an oxidant by dissolving in a second organic solvent, or is an oxidant; (3) the solution A and the solutionB are pumped into a micro-mixer of the micro-reaction device simultaneously for mixing, a product then flows into a microreactor of the micro-reaction device for reaction, and the disilane compounds are prepared, wherein the microreactor is filled with a catalyst. Raw materials required in the method are easily available and have better stability, metal copper compounds are used as a catalyst forcoupling reaction on trisubstituted silanes, and the coupling effect on trisubstituted silanes is better than that of alkali metal catalysts and transition metal catalysts; a micro-channel reactor issuitable for an exothermic coupling reaction due to good mixing and heat transfer performance.

PREPARATION OF SI-SI BOND-BEARING COMPOUNDS

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Page/Page column 3, (2009/05/28)

Si—Si bond-bearing compounds are effectively prepared by irradiating with radiation or heating Si—H group-bearing silicon compounds in organic solvents in the presence of iron complex catalysts. The Si—Si bond-bearing compounds are useful as a base material in photoresist compositions, ceramic precursor compositions, and conductive compositions.

Electroreductive Formation of Polysilanes

Shono, Tatsuya,Kashimura, Shigenori,Ishifune, Manabu,Nishida, Ryoichi

, p. 1160 - 1161 (2007/10/02)

Electroreduction of dichlorosilanes, such as 1,1-dichlorodialkylsilanes, 1,2-dichlorotetra-alkyldisilanes, and 1,4-bis(chlorodialkylsilyl)benzenes, with Mg electrodes in a single-compartment cell was found to yield the corresponding polysilanes.

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