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Silane, [[3,5-bis(1,1-dimethylethyl)-1,2-phenylene]bis(oxy)]bis[trimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

35188-68-2

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35188-68-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35188-68-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,1,8 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 35188-68:
(7*3)+(6*5)+(5*1)+(4*8)+(3*8)+(2*6)+(1*8)=132
132 % 10 = 2
So 35188-68-2 is a valid CAS Registry Number.

35188-68-2SDS

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 1,2-bis(trimethylsiloxy)-3,5-di-tert-butylbenzene

1.2 Other means of identification

Product number -
Other names 1,2-Bis-(trimethylsiloxy)-3,5-di-tert-butylbenzol

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:35188-68-2 SDS

35188-68-2Downstream Products

35188-68-2Relevant academic research and scientific papers

Reductive Silylation Using a Bis-silylated Diaza-2,5-cyclohexadiene

Beagan, Daniel M.,Huerfano,Polezhaev, Alexander V.,Caulton, Kenneth G.

, p. 8105 - 8111 (2019)

1,4-Bis(trimethylsilyl)-1,4-diaza-2,5-cyclohexadiene, 1, was tested as a reagent for the reductive silylation of various unsaturated functionalities, including N-heterocycles, quinones, and other redox-active moieties in addition to deoxygenation of main group oxides. Whereas most reactions tested are thermodynamically favorable, based on DFT calculations, a few do not occur, perhaps giving limited insight on the mechanism of this very attractive reductive process. Of note, reductive silylation reactions show a strong solvent dependence where a polar solvent facilitates conversions.

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