79750-76-8

Basic information

• Product Name: 1H-Imidazole, 2,5-dihydro-1-(4-methylphenyl)-2,4-diphenyl-, 3-oxide
• CAS NO: 79750-76-8
• Molecular Formula: C22H20N2O
• Molecular Weight: 328.414
• Mol File: 79750-76-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1H-Imidazole, 2,5-dihydro-1-(4-methylphenyl)-2,4-diphenyl-, 3-oxide(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Imidazole, 2,5-dihydro-1-(4-methylphenyl)-2,4-diphenyl-, 3-oxide(79750-76-8)
• EPA Substance Registry System: 1H-Imidazole, 2,5-dihydro-1-(4-methylphenyl)-2,4-diphenyl-, 3-oxide(79750-76-8)

Safety Data

• Hazardous Substances Data: 79750-76-8(Hazardous Substances Data)

Upstream product

• 14181-72-7 2-bromo-1-phenyl-ethanone oxime 
• 2272-45-9 benzal-p-toluidine 
• 100-52-7 benzaldehyde 
• 106-49-0 p-toluidine 
• 116546-08-8 N-Benzylidene-p-toluidine 
• 17082-14-3 syn-α-bromoacetophenone oxime 
• 51118-13-9 syn-(E)-α-(p-Toluidino)acetophenonoxim 
• 53181-18-3 ω-p-toluidino-acetophenone-β-oxime 

Downstream Products

• 79750-77-9 1-(4-methylphenyl)-2,4-diphenylimidazole 
• 20459-83-0 3-phenyl-4-methyl-1,2,4-oxadiazole-5(4H)-thione 
• 367262-86-0 C₃₂H₃₆N₂O 

Relevant articles and documents

A facile stereoselective synthesis of 2-perfluoroalkyl-3a,4,5,6-tetrahydroimidazo[1,5-b]isoxazoles

Methyl 2-perfluoroalkynoates 2 reacted readily with cyclic nitrones 1 via 1,3-dipolar cycloaddition at room temperature to give 2-perfluoroalkyl-3a,4,5,6-tetrahydroimidazo[1,5-b]isoxazoles 3 in good to excellent yields with high diastereoselectivity and r

Regio-and diastereoselective 1,3-dipolar cycloaddition of imidazoline 3-oxides to styrene

Δ3-lmidazoline 3-oxides (1) underwent regio- and diastereoselective cycloaddition with styrene to give perhydroimidazo[1,5-b]isoxazoles (3). Thermally induced retro cycloaddition of compounds (3) was demonstrated.

The Chemistry of Amino Oximes, XIV. Synthesis and Reaction of 2--3-imidazoline 3-Oxides

2-Benzoyl-4-phenyl-1-(p-tolyl)-3-imidazoline 3-oxide (3b) has been prepared by cyclocondensation of α-(p-toluidino)acetophenone oxime (1a) with phenylglyoxal and transferred into 2--4-phenyl-1-(p-tolyl)-3-imidazoline 3-oxide (5