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5,5,10,10-tetramethyl-5,10-dihydrosilanthrene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

33022-24-1

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33022-24-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33022-24-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,0,2 and 2 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 33022-24:
(7*3)+(6*3)+(5*0)+(4*2)+(3*2)+(2*2)+(1*4)=61
61 % 10 = 1
So 33022-24-1 is a valid CAS Registry Number.

33022-24-1SDS

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 5,5,10,10-tetramethylsilanthrene

1.2 Other means of identification

Product number -
Other names 9,9,10,10-tetramethyl-9,10-disilaanthracene

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:33022-24-1 SDS

33022-24-1Downstream Products

33022-24-1Relevant academic research and scientific papers

Fluorescence and phosphorescence of a series of silicon-containing six-membered-ring molecules

Nakashima, Takayuki,Shimada, Masaki,Kurihara, Yu,Tsuchiya, Mizuho,Yamanoi, Yoshinori,Nishibori, Eiji,Sugimoto, Kunihisa,Nishihara, Hiroshi

, p. 27 - 33 (2016)

Various silicon-containing six-membered-ring molecules were synthesized by Pd-catalyzed coupling reaction of 1,2-bis(dimethylsilyl)arenes with 1,2-diiodoarenes in moderate yields. Their optical properties were investigated via UV-vis absorption, fluorescence and phosphorescence spectroscopies, which indicated that the σ?-π?conjugated system expanded owing to the silicon atoms. Some of the compounds exhibited enhanced luminescence, larger Stokes shift, and phosphorescence in comparison with 9,9,10,10-tetramethyl-9,10-dihydroanthracene. Density functional theory (DFT) studies were also performed to investigate the photophysical properties of the compounds.

Countercation effect on reactivity of o-(fluorodimethylsilyl)phenyl anion

Kawachi, Atsushi,Teranishi, Takuya,Deguchi, Takuma,Yamamoto, Yohsuke

, p. 53 - 57 (2013/03/13)

The countercation effect on the reactivity of ambiphilic o-(fluorodimethylsilyl)phenyl anion was investigated by replacing Li in 1 with Cu (4 and 5), Mg (6), and Zn (7). The reactivity of the aryl metal species was estimated by the yields of dimerized pro

Preparation and oxidative coupling of bis[o-(hydrosilyl)phenyl]cuprates and bis[o-(fluorosilyl)phenyl]cuprates

Kawachi, Atsushi,Teranishi, Takuya,Yamamoto, Yohsuke

experimental part, p. 1226 - 1228 (2009/09/28)

Bis[o-(hydrosilyl)phenyl]cuprates and bis[o-(fluorosilyl)phenyl]cuprates were prepared by reacting [o-(hydrosilyl)phenyl]lithiums and [o-(fluorosilyl)phenyl]lithiums, respectively, with copper salts, such as CuCN and Cu(OPiv)2. The phenylcuprat

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