40608-86-4

Basic information

• Product Name: 2-(3-phenylpropyl)-1H-benzimidazole
• Synonyms: 2-(3-phenylpropyl)-1H-benzimidazole
• CAS NO: 40608-86-4
• Molecular Formula: C₁₆H₁₆N₂
• Molecular Weight: 236.31164
• Mol File: 40608-86-4.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(3-phenylpropyl)-1H-benzimidazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(3-phenylpropyl)-1H-benzimidazole(40608-86-4)
• EPA Substance Registry System: 2-(3-phenylpropyl)-1H-benzimidazole(40608-86-4)

Safety Data

• Hazardous Substances Data: 40608-86-4(Hazardous Substances Data)

Usage

Chemical class

Benzimidazoles

Physical form

White to off-white solid

Therapeutic use

Anti-inflammatory and analgesic agent

Mechanism of action

Inhibition of inflammatory mediator release

Potential anti-cancer properties

Yes

Application in inorganic and coordination chemistry

Yes, acts as a ligand and chelating agent with metal ions

Potential applications

Pharmaceutical, biomedical, and chemical industries

Ongoing research

Exploring various properties and potential uses.

Upstream product

• 18328-11-5 3-benzyl propionaldehyde 
• 95-54-5 1,2-diamino-benzene 
• 1821-12-1 4-Phenylbutyric acid 

Relevant articles and documents

Fe3O4@SiO2@polyionene/Br3- core-shell-shell magnetic nanoparticles: A novel catalyst for the synthesis of imidazole derivatives under solvent-free conditions

New Fe3O4@SiO2@polyionene/Br3- core-shell-shell magnetite nanoparticles were prepared using a co-precipitation method and were used in the syntheses of imidazole derivatives under solvent-free conditions. The polyionene was easily prepared by reacting DABCO and 1,4-dibromo butane in DMF/methanol. It was then added to the previously formed layers and magnetic core-shell nanoparticles (P-MNPs) were functionalized. All the resultant nanoparticles were characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), infrared spectroscopy (FTIR), X-ray diffraction (XRD), thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), and vibrating sample magnetometry (VSM). The catalyst was readily recovered by simple magnetic decantation and can be recycled several times with no significant loss of catalytic activity.

Condensation reactions of 2-ethylbenzimidazole with aromatic aldehydes

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