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

31709-10-1

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31709-10-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31709-10-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,7,0 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 31709-10:
(7*3)+(6*1)+(5*7)+(4*0)+(3*9)+(2*1)+(1*0)=91
91 % 10 = 1
So 31709-10-1 is a valid CAS Registry Number.

31709-10-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-bromophenyl)-5-[4-[5-(4-bromophenyl)-1,3,4-oxadiazol-2-yl]phenyl]-1,3,4-oxadiazole

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:31709-10-1 SDS

31709-10-1Downstream Products

31709-10-1Relevant academic research and scientific papers

New series of blue-emitting and electron-transporting copolymers based on fluorene

Zhan, Xiaowei,Liu, Yunqi,Wu, Xia,Wang, Shuai,Zhu, Daoben

, p. 2529 - 2537 (2007/10/03)

A novel series of conjugated copolymers having oxadiazole, quinoline, quinoxaline, and phenylenecyanovinylene moieties in the main chain based on fluorene were synthesized in good yields by palladium-catalyzed Suzuki coupling reaction, a new approach different from the traditional polyhydrazide precursor route (oxadiazole-containing polymers), acid-catalyzed Friedlaender condensation reaction (polyquinolines), and Knoevenagel condensation polymerization (poly(phenylenecyanovinylene)). The thermal, electrochemical, and optical properties of these copolymers were examined. All these polymers possess excellent thermal stability with glass transition temperatures of 114-208 °C and onset decomposition temperatures of 387-415 °C. Cyclic voltammetry studies reveal that these copolymers possess low-lying LUMO energy levels ranging from -3.01 to -3.37 eV and low-lying HOMO energy levels ranging from -6.13 to -6.38 eV and may be promising candidates for electron-transporting or hole-blocking materials in light-emitting diodes. The polymers in thin films emit strong blue luminance around 414-476 nm with narrow bandwidth upon photoexcitation. Photoluminescence spectra of the polymers in the films are only red-shifted by 7-11 nm compared to those in the solution, indicating that the aggregation and the excimer fluorescence are suppressed.

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