56018-53-2

Basic information

• Product Name: 2-(4-methoxyphenyl)-1,3-diphenylimidazolidine
• Synonyms: 2-(4-Methoxyphenyl)-1,3-diphenylimidazolidine; 2-(4-Methoxy-phenyl)-1,3-diphenyl-imidazolidine; Imidazolidine, 2-(4-methoxyphenyl)-1,3-diphenyl-
• CAS NO: 56018-53-2
• Molecular Formula: C₂₂H₂₂N₂O
• Molecular Weight: 330.4229
• Mol File: 56018-53-2.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 505.7°C at 760 mmHg
• Flash Point: 148.1°C
• Density: 1.149g/cm³
• Vapor Pressure: 2.37E-10mmHg at 25°C
• Refractive Index: 1.62
• CAS DataBase Reference: 2-(4-methoxyphenyl)-1,3-diphenylimidazolidine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-methoxyphenyl)-1,3-diphenylimidazolidine(56018-53-2)
• EPA Substance Registry System: 2-(4-methoxyphenyl)-1,3-diphenylimidazolidine(56018-53-2)

Safety Data

• Hazardous Substances Data: 56018-53-2(Hazardous Substances Data)

Usage

General Description

2-(4-methoxyphenyl)-1,3-diphenylimidazolidine is a chemical compound that belongs to the imidazolidine family. It has a molecular formula of C21H20N2O and a molar mass of 312.399 g/mol. 2-(4-methoxyphenyl)-1,3-diphenylimidazolidine is a white solid at room temperature and is insoluble in water. It is commonly used in the field of organic synthesis and pharmaceutical research. Its structure consists of a 1,3-diphenylimidazolidine ring with a 4-methoxyphenyl group attached to one of the phenyl rings. The compound has potential applications as a chiral ligand in catalysis and as a building block for the synthesis of biologically active compounds.

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Relevant articles and documents

Synthesis and evaluation of antiinflammatory and analgesic activity of some new 1,3-diphenyl-2-aryltetrahydroimidazoles

In an effort to search for new antiinflammatory and analgesic agents, some new tetrahydroimidazole derivatives 2a-2g have been synthesized via condensation of 1,2-dianilinoethane with various aldehydes. Characterization of the newly synthesized compounds has been done on the basis of 1H NMR and mass spectral data. The resulting compounds have been evaluated for their antiinflammatory activity. The activity of compounds 2b and 2c is excellent and comparable to indomethacin. All these compounds have been tested for their analgesic activity also and their LD50 determined. Compounds 2b and 2c show a comparable activity with aspirin. The MTD for all the compounds is found to be >1800 mg/kg.

BENTONITE K10 CLAY, AN EFFICIENT CATALYST FOR THE FORMATION OF NITROGEN DERIVATIVES

Bentonite K10 clay has been used to catalyze the formation of enamino carbonyl derivatives, 2-methyl-1H-benzimidazoles, Hantzsch 1,4-dihydropyridines, Hantzsch pyridines, 2-substituted 1,3-diphenylimidazolidines, and tetrahydropyranylbenzazoles.