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1,2,4,5-Tetramethyl-3,6-bis-trimethylsilanyloxy-benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82363-84-6

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82363-84-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82363-84-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,3,6 and 3 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 82363-84:
(7*8)+(6*2)+(5*3)+(4*6)+(3*3)+(2*8)+(1*4)=136
136 % 10 = 6
So 82363-84-6 is a valid CAS Registry Number.

82363-84-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name ((2,3,5,6-tetramethyl-1,4-phenylene)bis(oxy))bis(trimethylsilane)

1.2 Other means of identification

Product number -
Other names -

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:82363-84-6 SDS

82363-84-6Downstream Products

82363-84-6Relevant academic research and scientific papers

Highly efficient and chemoselective reductive bis-silylation of quinones by silyltellurides

Yamago, Shigeru,Miyazoe, Hiroshi,Iida, Kazunori,Yoshida, Jun-Ichi

, p. 3671 - 3673 (2007/10/03)

(matrix presented) Silyltellurides serve as new silicon-based chemoselective reducing agents and reduce quinones to the corresponding bis-silylated hydroquinones. The reaction proceeds under ambient thermal conditions without the need of any additional promoters or catalysts and gives the products in excellent yields. Several control experiments suggest that the reaction is initiated by a single electron transfer from silyltellurides to quinones.

Novel Catalysis of Hydroquinone Autoxidation with Nitrogen Oxides

Bosch, E.,Rathore, R.,Kochi, J. K.

, p. 2529 - 2536 (2007/10/02)

An efficient catalytic method is described for the preparative conversion of hydroquinones to quinones with dioxygen under mild conditions.The use of the gaseous nitrogen oxide (NOx) catalyst allows a simple workup procedure for the isolation of quinones in essentially quantitative yields by merely removing the low-boiling solvent dichloromethane in vacuo.The mechanism of the catalytic autoxidation of hydroquinones is ascribed to the critical role of nitrosonium (NO(+)) in the one-electron oxidation of hydroquinone, followed by the reoxidation of the reduced nitric oxide (NO) with dioxygen.An extensive series of complex interchanges among various NOx species in nitrogen-(V), -(IV), -(III), and -(II) oxidation states, coupled with stepwise oxidation of hydroquinone via a successive series of one-electron/proton transfer, from the critical components of the catalytic cycle.

A NEW REDUCTIVE SILYLATION OF p-QUINONES WITH HEXAMETHYLDISILANE CATALYZED BY IODINE

Matsumoto, Hideyuki,Koike, Shunji,Matsubara, Ikuya,Nakano, Taichi,Nagai, Yoichiro

, p. 533 - 534 (2007/10/02)

In the presence of a catalytic amount of iodine, hexamethyldisilane can reductively silylate p-quinones under mild conditions to afford 1,4-bis(trimethylsiloxy)arenes in high yields.

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