1740-26-7

Basic information

• Product Name: 2-(2-fluorophenyl)-4,5-diphenyl-1H-imidazole
• Synonyms: 2-(2-fluorophenyl)-4,5-diphenyl-1H-imidazole
• CAS NO: 1740-26-7
• Molecular Weight: 314.362
• Mol File: 1740-26-7.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: 2-(2-fluorophenyl)-4,5-diphenyl-1H-imidazole(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-fluorophenyl)-4,5-diphenyl-1H-imidazole(1740-26-7)
• EPA Substance Registry System: 2-(2-fluorophenyl)-4,5-diphenyl-1H-imidazole(1740-26-7)

Safety Data

• Hazardous Substances Data: 1740-26-7(Hazardous Substances Data)

Upstream product

• 119-53-9 2-hydroxy-2-phenylacetophenone 
• 446-52-6 2-Fluorobenzaldehyde 
• 501-65-5 diphenyl acetylene 
• 24242-77-1 α-iodo-α-phenylacetophenone 
• 134-81-6 benzil 
• 446-51-5 2-fluorobenzyl alcohol 
• 451-40-1 phenyl benzyl ketone 

Relevant articles and documents

One-Pot, Two-Step Metal and Acid-Free Synthesis of Trisubstituted Imidazole Derivatives via Oxidation of Internal Alkynes Using an Iodine/DMSO System

A one-pot, two-step, simple, efficient and eco-friendly oxidation of internal alkynes as a key step towards the synthesis of 2,4,5-trisubstituted imidazoles, using an inexpensive I2/DMSO system, has been reported. This metal and acid-free synthesis proceeded smoothly to furnish a variety of synthetically useful trisubstituted imidazoles in moderate to excellent yields. In an effort to demonstrate the potential future applications of this system, a double oxidation study was undertaken and the desired trisubstituted imidazoles obtained in good to moderate yields.

An eco-friendly, one pot synthesis of tri-substituted imidazoles in aqueous medium catalyzed by RGO supported Au nano-catalyst and computational studies

An eco-compatible, mild and operationally simple aqueous phase protocol for the synthesis of 2,4,5-trisubstituted imidazoles has been achieved with high substrate scope using supported Au nanoparticles. The catalyst can be recovered for the subsequent rea

An efficient multicomponent synthesis of 2,4,5-trisubstituted and 1,2,4,5-tetrasubstituted imidazoles catalyzed by a magnetic nanoparticle supported Lewis acidic deep eutectic solvent

A mild and highly efficient reaction for the synthesis of 2,4,5-trisubstituted and 1,2,4,5-tetrasubstituted imidazoles catalyzed by a magnetically supported Lewis acidic deep eutectic solvent on magnetic nanoparticles (LADES?MNP) has been developed via one-pot multicomponent processes under solvent-free sonication. These reactions have good to excellent yields, mild conditions, and work-up simplicity. This method represents a new method for the preparation of 2,4,5-trisubstituted and 1,2,4,5-tetrasubstituted imidazoles. More importantly, LADES?MNP can be easily recovered by magnetic separation and reused five times without significant loss of catalytic activity.