2622-70-0

Usage

Molecular structure

Contains a benzimidazole core, a phenyl group, and a fluorophenyl group.

Classification

Benzimidazole derivative

Usage

Commonly used in organic synthesis and medicinal chemistry

Potential applications

Development of new drugs and pharmaceuticals

Industrial uses

Production of specialty chemicals and materials

Versatility

Promising potential for research and development in various fields

Upstream product

• 140-75-0 para-fluorobenzylamine 
• 534-85-0 N-phenyl-1,2-benzenediamine 
• 459-57-4 4-fluorobenzaldehyde 
• 403-43-0 4-fluorobenzoyl chloride 

Relevant academic research and scientific papers

Fluorescence quenching of organic molecule by insulator

A new kind of fluorophore 2-(4-fluorophenyl)-1-phenyl-1H-benzo[d]imidazole (FPPBI) has been synthesized and characterized by 1H NMR, 13C NMR, mass spectral studies and single crystal XRD. The energy transfer from FPPBI to Al 2O3 nanocrystals has been studied by absorption, fluorescence and lifetime spectroscopic methods. The association between nanoparticles and FPPBI is explained from both absorption and fluorescence quenching data. The distance between FPPBI and Al2O3 as well as the critical energy transfer distance has been deduced.

Novel bluish green benzimidazole-based iridium(III) complexes for highly efficient phosphorescent organic light-emitting diodes

Three multifluorinated benzimidazole-based iridium [Ir(iii)] complexes abbreviated as 1F-Ir, 2F-Ir, and 3F-Ir were designed and synthesized. Their photoluminescent, thermal, and electrochemical properties were investigated in detail. These Ir(iii) complex

A Bioinspired Catalytic Aerobic Oxidative C-H Functionalization of Primary Aliphatic Amines: Synthesis of 1,2-Disubstituted Benzimidazoles

Aerobic oxidative C-H functionalization of primary aliphatic amines has been accomplished with a biomimetic cooperative catalytic system to furnish 1,2-disubstituted benzimidazoles that play an important role as drug discovery targets. This one-pot atom-economical multistep process, which proceeds under mild conditions, with ambient air and equimolar amounts of each coupling partner, constitutes a convenient environmentally friendly strategy to functionalize non-activated aliphatic amines that remain challenging substrates for non-enzymatic catalytic aerobic systems.

Synthesis of some fluorescent benzimidazole derivatives using cobalt(ii) hydroxide as highly efficient catalyst-spectral and physico-chemical studies and ESIPT process

Some fluorescent benzimidazole derivatives have been designed and synthesized using cobalt(ii) hydroxide as highly efficient catalyst. Synthesized compounds have been characterized by 1H and 13C-NMR and mass spectral analysis. The so

Optical properties of 1,2-diaryl benzimidazole derivatives - A combined experimental and theoretical studies

Some novel 1,2-diaryl benzimidazole derivatives have been designed, synthesized and characterized by mass, 1H, 13C-NMR spectral studies and single crystal XRD. The charge distribution has been calculated from the atomic charges by no

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

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

Iridium complexes as light emitting materials and organic light emitting diode device

Phosphorescent iridium complexes having Formula I or Formula II: wherein X is chosen from a monoanionic bidentate ligand; Z is chosen from an atomic group wherein Z together with the buta-1,3-diene to which Z is attached form an aryl group or heteroaryl group; R, R1, and R2 are independently chosen from a hydrogen atom or a substituent; m is an integer from 0 to 4; and n is an integer from 0 to the maximum number of possible substituents on Z, are disclosed. Light emitting devices using the phosphorescent iridium complexes are also disclosed.

Organometallic complex for organic electroluminescent device

An organometallic complex having formula (I) wherein M is a transition metal; each A1 and A2 is independently a monodentate ligand, or A1 and A2 are covalently joined together to form a bidentate ligand; R1