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2,2'-Bithiophene, 3,3'-bis[3,5-bis(1,1-dimethylethyl)-4-methoxyphenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

928306-64-3

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928306-64-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 928306-64-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,8,3,0 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 928306-64:
(8*9)+(7*2)+(6*8)+(5*3)+(4*0)+(3*6)+(2*6)+(1*4)=183
183 % 10 = 3
So 928306-64-3 is a valid CAS Registry Number.

928306-64-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(3,5-ditert-butyl-4-methoxyphenyl)-2-[3-(3,5-ditert-butyl-4-methoxyphenyl)thiophen-2-yl]thiophene

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:928306-64-3 SDS

928306-64-3Downstream Products

928306-64-3Relevant academic research and scientific papers

Raman spectroscopic characterization of a thiophene-based active material for resistive organic nonvolatile memories

Fazzi, Daniele,Canesi, Eleonora Valeria,Bertarelli, Chiara,Castiglioni, Chiara,Negri, Fabrizia,Zerbi, Giuseppe

, p. 406 - 413 (2011/12/04)

A combined theoretical and experimental Raman study is presented on a diphenyl bithiophene molecule known as a good candidate for the development of organic nonvolatile memory devices. Spectroscopic markers suitable to distinguish the different stable conformers of the molecule have been predicted and detected. The combined analysis of theoretical and experimental Raman spectra recorded in solution indicates that at room temperature a dynamical equilibrium, characterized by interconversion between the two more stable conformers (namely trans and cis), takes place and that the more populated species is the cis form. Referring to the solid phase instead, Raman spectra of single-crystal samples show the presence of the only trans conformer, as confirmed by X-ray measurements. Finally, Raman spectra of thin films, as those used for the memory device, were collected; samples just deposited from solution and after few hours from the deposition were analyzed. Following the evolution of selective spectroscopic Raman markers, an isomerization process from the abundant cis (as-deposited) to the totally trans (after few hours) conformer in the solid phase was detected. These results open the way to the identification of the molecular isomers present in the tthin film of the memory cell and finally of the active molecular species involved in the switching mechanism of the operating device.

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