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1H-Benzimidazole, 2-(3,5-dibromophenyl)-1-phenylis a heterocyclic chemical compound that belongs to the benzimidazole derivatives class. It features a benzene ring fused to an imidazole ring, with two bromine atoms attached to the phenyl group. 1H-BenziMidazole, 2-(3,5-dibroMophenyl)-1-phenylhas potential pharmacological activities and is being explored for its use in various therapeutic applications. Its unique chemical structure and properties make it a promising candidate for research in medicinal chemistry, with potential applications in treating certain diseases or conditions.

953091-79-7

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953091-79-7 Usage

Uses

Used in Pharmaceutical Research:
1H-Benzimidazole, 2-(3,5-dibromophenyl)-1-phenylis used as a drug candidate for its potential therapeutic applications in treating specific diseases or conditions. Its unique chemical structure and pharmacological properties make it a subject of interest for further investigation in medicinal chemistry.
Used in Medicinal Chemistry:
1H-Benzimidazole, 2-(3,5-dibromophenyl)-1-phenylis utilized as a compound of interest in medicinal chemistry research. Its potential as a drug candidate and its unique chemical properties contribute to the development of new therapeutic agents and the advancement of pharmaceutical science.
Overall, 1H-Benzimidazole, 2-(3,5-dibromophenyl)-1-phenylis a compound with diverse potential applications in the fields of chemistry and pharmaceutical research, warranting further investigation and development.

Check Digit Verification of cas no

The CAS Registry Mumber 953091-79-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,3,0,9 and 1 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 953091-79:
(8*9)+(7*5)+(6*3)+(5*0)+(4*9)+(3*1)+(2*7)+(1*9)=187
187 % 10 = 7
So 953091-79-7 is a valid CAS Registry Number.

953091-79-7SDS

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 2-(3,5-dibromophenyl)-1-phenylbenzimidazole

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

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More Details:953091-79-7 SDS

953091-79-7Relevant academic research and scientific papers

Substituted 1,3,5-triazine compound, composition and application thereof

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Paragraph 0144-0146, (2020/10/16)

The invention discloses a substituted 1,3,5-triazine compound, a composition and application thereof. The 1,3,5-triazine compound shown as a formula I is provided by the invention, can be used as an electron transport material and, can be used as an electron acceptor material. The composition that can be used for preparing an electron transport layer or an electron donor material is used as a mainbody material of an electroluminescent device, so that the prepared electroluminescent device has the advantages of relatively high efficiency, relatively long service lifetime and the like. As the 1,3,5-triazine compound is used as an electron transport layer, the composition used as an electron acceptor material and an electron donor material is adopted to construct a light-emitting layer, andthe prepared electroluminescent device has the advantages of higher efficiency, longer service lifetime and the like.

Copolyphenylenes with pendant benzimidazolyl and diethanolaminohexyloxy groups: Synthesis and electron-transporting application in PLEDs

Tseng, Chih-Yang,Su, Wen-Fen,Chen, Yun

, p. 2494 - 2505 (2017/06/23)

Two new electron-transporting copolyphenylenes P1NH and P2NH possessing balanced charges crucial to emission efficiency of polymer light-emitting diodes (PLEDs) have been synthesized and applied as an electron-transporting layer (ETL). The main chain structure is all para-linkage for P1NH and both para- and meta-linkage for P2NH, with the same pendant electron-withdrawing benzimidazolyl and polar diethanolaminohexyloxy groups. Both copolymers possess excellent thermal stability (Td > 300 °C, Tg > 100 °C) due to their rigid backbones. In addition, the pendant groups effectively lower LUMO (~ ?2.70 eV) and HOMO (~ ?5.70 eV) levels, resulting in improved electron-transporting and hole-blocking capabilities. Multilayer yellow-emitting PLEDs with a configuration of ITO/PEDOT:PSS/SY/ETL/LiF/Al were successfully fabricated by the spin-coating process. The maximum luminance and maximum current efficiency of the P1NH-based device were 12,881 cd/m2 and 10.94 cd/A, respectively, superior to the performance of P2NH-based device (4938 cd/m2, 3.70 cd/A) and the device without ETL (8690 cd/m2, 2.78 cd/A). Current results indicate that P1NH is highly effective in enhancing electron transport and device performance.

NOVEL COMPOUNDS FOR AN ORGANIC PHOTOELECTRIC DEVICE, AND ORGANIC PHOTOELECTRIC DEVICE COMPRISING SAME

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Page/Page column, (2014/12/12)

A novel compound for an organic photoelectric device and an organic photoelectric device including the same are provided. The compound is represented by Chemical Formula 1. The compound according to one embodiment of the present invention can act as a hol

COMPOUND FOR ORGANIC PHOTOELECTRIC DEVICE, ORGANIC PHOTOELECTRIC DEVICE INCLUDING THE SAME, AND DISPLAY DEVICE INCLUDING THE SAME

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, (2011/11/06)

A compound for an organic photoelectric device, an organic photoelectric device including the same, and a display device including the same the compound being represented by the following Chemical Formula 1:

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