2620-84-0

Basic information

• Product Name: 1H-Benzimidazole, 2-(4-methoxyphenyl)-1-phenyl-
• CAS NO: 2620-84-0
• Molecular Formula: C20H16N2O
• Molecular Weight: 300.36
• Mol File: 2620-84-0.mol
• Article Data: 17

Chemical Properties

• CAS DataBase Reference: 1H-Benzimidazole, 2-(4-methoxyphenyl)-1-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Benzimidazole, 2-(4-methoxyphenyl)-1-phenyl-(2620-84-0)
• EPA Substance Registry System: 1H-Benzimidazole, 2-(4-methoxyphenyl)-1-phenyl-(2620-84-0)

Safety Data

• Hazardous Substances Data: 2620-84-0(Hazardous Substances Data)

Usage

Chemical structure

A benzimidazole derivative with a phenyl and a 4-methoxyphenyl group

Application

Pharmaceutical research

Use

Building block for the synthesis of potential drug candidates

Pharmacological properties

Antifungal, antitumor, and anti-inflammatory activities

Biological activities

Under investigation

Therapeutic uses

Potential applications in drug discovery and development

Structural characteristics

Valuable target for medicinal chemistry and drug design studies

Upstream product

• 2393-23-9 4-methoxy-benzylamine 
• 534-85-0 N-phenyl-1,2-benzenediamine 
• 874-90-8 4-methoxybenzonitrile 
• 62-53-3 aniline 
• 4450-64-0 N₁-phenyl-4-methoxy-1-benzenecarboximidamide 
• 108-94-1 cyclohexanone 
• 17004-42-1 1,2-bis(4-methoxybenzyl)disulfide 
• 794-94-5 p-Methoxybenzoic anhydride 
• 161455-84-1 4-methoxy-N-(2-(phenylamino)phenyl)benzamide 
• 100-07-2 4-methoxy-benzoyl chloride 
• 100-09-4 4-methoxybenzoic acid 
• 123-11-5 4-methoxy-benzaldehyde 
• 105-64-6 diisopropyl peroxydicarbonate 

Downstream Products

• 175713-98-1 1-phenyl-2-[4-[3-(piperidin-1-yl)propoxy]phenyl]-benzimidazole 
• 175713-97-0 1-phenyl-2-(4-(2-(piperidin-1-yl)ethoxy)phenyl)-1H-benzo[d]imidazole 
• 94212-06-3 4-(1-phenyl-1H-benzo[d]imidazol-2-yl)phenol 

Relevant articles and documents

Molecular Engineering of Phenylbenzimidazole-Based Orange Ir(III) Phosphors toward High-Performance White OLEDs

To develop B-O complementary-color white organic light-emitting diodes (WOLEDs) exhibiting high efficiency and low roll-off as well as color stability simultaneously, we have designed two orange iridium(III) complexes by simply controlling the position of

Sulfur-Catalyzed Oxidative Coupling of Dibenzyl Disulfides with Amines: Access to Thioamides and Aza Heterocycles

In the presence of catalytic amounts of elemental sulfur, dibenzyl disulfide/DMSO was found to be an excellent thiobenzoylating agent of amines to provide a wide range of thioamides. The reaction becomes autocatalytic when anilines substituted by an o-cyclizable group were used as nucleophile, leading to the corresponding 2-aryl aza heterocycles. (Figure presented.).

METHOD FOR THE SYNTHESIS OF BENZAZOLE

PROBLEM TO BE SOLVED: To obtain a benzazole in a short reaction time with high yields. SOLUTION: A method for the synthesis of a benzazole includes a chemical reaction represented by the chemical reaction formula (1) to occur in subcritical water or supercritical water (X is NR6, O, or S. Y is H, OR7, halogen, or NR8R9. R1 to R9 are a C1-C20 aliphatic or aromatic substituent which may have O, N, S, B, Si, halogen, or P (two or more substituents of R1 to R6 may be coupled together, R8 and R9 may be coupled together, and two or more substituents of R1 to R9 may be the same) or H). SELECTED DRAWING: None COPYRIGHT: (C)2017,JPOandINPIT