117215-39-1

Basic information

• Product Name: (4,5-bis(4-methoxyphenyl)-1H-imidazol-2-yl)(phenyl)methanone
• Synonyms: (4,5-bis(4-methoxyphenyl)-1H-imidazol-2-yl)(phenyl)methanone
• CAS NO: 117215-39-1
• Molecular Weight: 384.434
• Mol File: 117215-39-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (4,5-bis(4-methoxyphenyl)-1H-imidazol-2-yl)(phenyl)methanone(CAS DataBase Reference)
• NIST Chemistry Reference: (4,5-bis(4-methoxyphenyl)-1H-imidazol-2-yl)(phenyl)methanone(117215-39-1)
• EPA Substance Registry System: (4,5-bis(4-methoxyphenyl)-1H-imidazol-2-yl)(phenyl)methanone(117215-39-1)

Safety Data

• Hazardous Substances Data: 117215-39-1(Hazardous Substances Data)

Upstream product

• 1226-42-2 1,2-bis(4-methoxyphenyl)-1,2-ethanedione 
• 22397-48-4 4,5-bis(4-methoxyphenyl)-1H-imidazole 
• 98-88-4 benzoyl chloride 
• 119-52-8 4,4'-dimethoxybenzoin 
• 98-86-2 acetophenone 

Downstream Products

• 1309776-36-0 2,3,6-tri(4-methoxyphenyl)-8-phenylimidazo[1,2-a]pyrazine 
• 1309775-99-2 1-(2-phenyl-2-oxoethyl)-2-benzoyl-4,5-di(4-methoxyphenyl)imidazole 
• 1309776-35-9 2,3-di(4-methoxyphenyl)-6,8-diphenylimidazo[1,2-a]pyrazine 
• 1309776-00-8 1-(2-(4-methoxyphenyl)-2-oxoethyl)-2-benzoyl-4,5-di(4-methoxyphenyl)imidazole 
• 1309776-01-9 1-(2-(4-chlorophenyl)-2-oxoethyl)-2-benzoyl-4,5-di(4-methoxyphenyl)imidazole 

Relevant articles and documents

Investigation of synthesis and some properties of the copper complexes containing imidazole ligand

The copper(II) complexes bearing tetrasubstituted imidazole derivatives containing oxygen donor as ligands (L1-6) were synthesized and characterized by spectroscopic methods, magnetic measurements, elemental and thermogravimetric analyses. The

Synthesis of some 2,3,6,8-tetraarylimidazo[1,2-a]pyrazine derivatives by using either reflux or microwave irradiation method, and investigation their anticancer activities

In this study, some 2,3,6,8-tetraarylimidazo[1,2-a]pyrazine derivatives were synthesized by reacting 1-(2-aryl-2-oxoethyl)-2-aryloyl-4,5- diarylimidazoles from 2-aryloyl-4,5-diarylimidazole and 2-bromoacetophenone derivatives with ammonium acetate in acetic acid by using the method that was previously developed and repeatedly tested in our studies. Structural elucidation of the compounds was performed by IR, 1H-NMR, and MASS spectroscopic data and elemental analysis results. Anticancer activities of selected compounds were evaluated and the noticeable activity values were reported.