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760212-40-6

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760212-40-6 Usage

Description

2-(3-bromophenyl)-1-phenyl-1H-benzimidazole is a chemical compound belonging to the benzimidazole family of organic compounds. It is characterized by the presence of a bromine atom attached to the third carbon of the phenyl group, making it a brominated derivative. The benzimidazole structure of the compound provides high thermal stability and resistance to oxidation.

Uses

Used in Pharmaceutical Industry:
2-(3-bromophenyl)-1-phenyl-1H-benzimidazole is used as a pharmaceutical compound for its potential biological activities. The specific structure of the compound allows for modification to enhance its therapeutic properties and target various biological pathways.
2-(3-bromophenyl)-1-phenyl-1H-benzimidazole's high thermal stability and resistance to oxidation make it suitable for use in pharmaceutical formulations, ensuring its stability and efficacy during manufacturing and storage processes.
Furthermore, the brominated derivative nature of 2-(3-bromophenyl)-1-phenyl-1H-benzimidazole may contribute to its unique biological activities, such as modulating specific signaling pathways or interacting with certain receptors, making it a promising candidate for the development of new drugs and therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 760212-40-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,0,2,1 and 2 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 760212-40:
(8*7)+(7*6)+(6*0)+(5*2)+(4*1)+(3*2)+(2*4)+(1*0)=126
126 % 10 = 6
So 760212-40-6 is a valid CAS Registry Number.
InChI:InChI=1/C19H13BrN2/c20-15-8-6-7-14(13-15)19-21-17-11-4-5-12-18(17)22(19)16-9-2-1-3-10-16/h1-13H

760212-40-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-Bromophenyl)-1-phenyl-1H-benzoimidazole

1.2 Other means of identification

Product number -
Other names 2-(3-bromophenyl)-1-phenylbenzimidazole

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:760212-40-6 SDS

760212-40-6Relevant articles and documents

Electron transporting and hole blocking organic material and application thereof in thin-film light-emitting diode

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Paragraph 0005, (2020/11/02)

The invention provides an electron transporting and hole blocking material with an A-D-A link structure as a core. The material is applied to a thin-film semiconductor light-emitting diode, for example, an organic light-emitting diode and a quantum dot thin-film light-emitting diode; and the molecule of the material takes bipolar carbazole and a derivative group thereof as electron donating centers, so a relatively high triplet state energy level can be maintained to ensure exciton blocking capability.

Achieving High Performances of Nondoped OLEDs Using Carbazole and Diphenylphosphoryl-Functionalized Ir(III) Complexes as Active Components

Mao, Hui-Ting,Zang, Chun-Xiu,Shan, Guo-Gang,Sun, Hai-Zhu,Xie, Wen-Fa,Su, Zhong-Min

supporting information, p. 9979 - 9987 (2017/08/26)

Nondoped electroluminescent devices offer advantages over their doped counterparts such as good reproducibility, reduced phase separation between host and guest materials, and potential of lower-cost devices. However, low luminance efficiencies and signif

An organic electron transport compound

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, (2016/10/07)

The invention provides an organic electronic transmission compound having a following structural formula (I) as shown in the specification. The organic electronic transmission compound is better in thermal stability, is high in luminous efficiency and purity, can be used for manufacturing an organic electroluminescence device and is applied to the field of organic solar batteries, organic thin film transistors or organic photoreceptors..

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