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Benzenamine, 2,4-dibromo-6-(phenylazo)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

70593-69-0

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70593-69-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70593-69-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,5,9 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 70593-69:
(7*7)+(6*0)+(5*5)+(4*9)+(3*3)+(2*6)+(1*9)=140
140 % 10 = 0
So 70593-69-0 is a valid CAS Registry Number.

70593-69-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-dibromo-6-phenyldiazenylaniline

1.2 Other means of identification

Product number -
Other names Benzenamine,2,4-dibromo-6-(phenylazo)

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:70593-69-0 SDS

70593-69-0Relevant academic research and scientific papers

Bipyridyl-substituted benzo[1,2,3]triazoles as a thermally stable electron transporting material for organic light-emitting devices

Ichikawa, Musubu,Mochizuki, Shunji,Jeon, Hyeon-Gu,Hayashi, Shuichi,Yokoyama, Norimasa,Taniguchi, Yoshio

experimental part, p. 11791 - 11799 (2011/10/31)

We developed new electron-transporting materials (ETMs) for organic light-emitting devices (OLEDs) based on benzo[1,2,3]triazole and two bipyridines. Four derivatives based on the same skeleton were synthesized with four different substituents: phenyl (BpyBTAZ-Ph), biphenyl (-BP), m-terphenyl (-mTP), and o-terphenyl (-oTP). These BpyBTAZ compounds have good thermal stabilities, and their decomposition temperatures were greater than 410 °C, which is significantly higher than that of tris(8-quinolinolato)aluminium (Alq), the conventional OLED material. BpyBTAZ compounds show preferable amorphous nature, and moreover, the glass transition temperatures (Tgs) of both BpyBTAZ-TP compounds exceed 100 °C. Furthermore, BpyBTAZ-BP exhibits no melting point and is fully amorphous. The electron affinities of the materials are as large as 3.3 eV and their electron mobility is sufficiently high. These characteristics accounted for a reduction in the operational voltage of OLEDs with BpyBTAZ compounds compared with the reference device with Alq as an ETM. Specifically, the electron mobility of all the BpyBTAZ compounds exceeds 1 × 10-4 cm2 V-1 s-1 at an electric field of 1 MV cm-1. In addition, it was revealed that both BpyBTAZ-TP-based devices showed longer luminous lifetimes and smaller voltage increases during continuous operation at 50 mA cm-2, compared with the Alq reference device. The Royal Society of Chemistry 2011.

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