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2-(1-naphthalenyl)-1-phenyl-benzimidazole is a complex organic compound with the molecular formula C24H17N. It is a derivative of benzimidazole, which is a heterocyclic aromatic organic compound consisting of a benzene ring fused to an imidazole ring. This particular compound features a naphthalene group (a fused pair of benzene rings) at the 2-position and a phenyl group (a single benzene ring) at the 1-position of the benzimidazole core. It is known for its potential applications in the field of materials science, particularly as a luminescent material or in the development of organic light-emitting diodes (OLEDs) due to its electronic and optical properties. The compound's structure endows it with unique photophysical characteristics, making it a subject of interest for researchers in the field of organic chemistry and materials science.

2562-84-7

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2562-84-7 Usage

Fluorescent properties

NPBI emits light upon excitation, making it useful in fluorescence spectroscopy and imaging studies.

Antimicrobial properties

Research has shown that NPBI exhibits antimicrobial properties, suggesting its potential as an antibacterial agent.

Photodynamic therapy

NPBI has been investigated for its potential use as a photosensitizer in cancer treatment.

Check Digit Verification of cas no

The CAS Registry Mumber 2562-84-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,6 and 2 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2562-84:
(6*2)+(5*5)+(4*6)+(3*2)+(2*8)+(1*4)=87
87 % 10 = 7
So 2562-84-7 is a valid CAS Registry Number.

2562-84-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-naphthalen-1-yl-1-phenylbenzimidazole

1.2 Other means of identification

Product number -
Other names 2-naphthalen-1-yl-1-phenyl-1H-benzoimidazole

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:2562-84-7 SDS

2562-84-7Downstream Products

2562-84-7Relevant academic research and scientific papers

Benzimidazoles: A new class of carbonic anhydrase inhibitors

Khan, Khalid Mohammed,Khan, Momin,Saleem, Muhammad,Taha, Muhammad,Perveen, Shahnaz,Choudhary, Mohammad Iqbal

, p. 901 - 904 (2013/07/26)

Carbonic anhydrase inhibitory activity of benzimidazole derivatives 1-24 has been evaluated. Compounds 22 (IC50 = 7.47 ± 0.39 μM), 21 (IC50 = 10.31 ± 0.11 μM), 20 (IC50 = 23.1 ± 1.78 μM), 12 (IC50 = 12.16 ± 0.10

Conventional and microwave-assisted synthesis of benzimidazole derivatives and their in vitro inhibition of human cyclooxygenase

Secci, Daniela,Bolasco, Adriana,D'Ascenzio, Melissa,Della Sala, Flavio,Yanez, Matilde,Carradori, Simone

, p. 1187 - 1195 (2013/01/15)

A large series of 1,2-diaryl-benzimidazole and 2-aryl-1H-benzimidazole derivatives were synthesized with slight differences using both microwave irradiation and conventional heating methods. Usually higher yields and time reactions reduction were obtained

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