49738-18-3

Basic information

• Product Name: imidazolidine-1,3-diylbis(phenylmethanone)
• Synonyms: methanone, 1,1'-(1,3-imidazolidinediyl)bis[1-phenyl-
• CAS NO: 49738-18-3
• Molecular Formula: C₁₇H₁₆N₂O₂
• Molecular Weight: 280.3211
• Mol File: 49738-18-3.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 484.2°C at 760 mmHg
• Flash Point: 226.2°C
• Density: 1.246g/cm³
• Vapor Pressure: 1.57E-09mmHg at 25°C
• Refractive Index: 1.632
• CAS DataBase Reference: imidazolidine-1,3-diylbis(phenylmethanone)(CAS DataBase Reference)
• NIST Chemistry Reference: imidazolidine-1,3-diylbis(phenylmethanone)(49738-18-3)
• EPA Substance Registry System: imidazolidine-1,3-diylbis(phenylmethanone)(49738-18-3)

Safety Data

• Hazardous Substances Data: 49738-18-3(Hazardous Substances Data)

Upstream product

• 50-00-0 formaldehyd 
• 644-33-7 N,N'-ethanediyl-bis-benzamide 
• 110-88-3 1,3,5-Trioxan 
• 628-51-3 diacetoxymethane 
• 107-30-2 chloromethyl methyl ether 
• 109-87-5 Dimethoxymethane 
• 504-74-5 tetrahydroimidazole 
• 98-88-4 benzoyl chloride 

Downstream Products

• 116046-94-7 1,3-dibenzoyl-2-methylimidazolidine 
• 116046-95-8 1,2,3-tribenzoylimidazolidine 

Relevant articles and documents

N,N'-bisacylimidazolidines from 1,2-diamines

A variety of novel 1,3-bisacylimidazolidines were prepared in a one-pot procedure from 1,2-diamines. Condensation of 1,2-diaminoethane or a selection of chiral 1,2-diamines with a variety of aldehydes under dehydrating conditions gives rise to 1,3-bisunsubstituted imidazolidines. These imidazolidines were not isolated, but were treated with acid chlorides or anhydrides to give the novel 1,3-bisacylimidazolidines.

Acyl Derivatives of Cyclic Secondary Amines. Part 1. Dipole Stabilization of Anions: the Cumulative effect of Two Stabilizing Groups

Lithiation studies with diacylimidazolidines, diacylhexahydropyrimidines, and triacylhexahydro-1,3,5-triazines indicate that no substantial increase in carbanion stability occurs as a result of the introduction of the second stabilizing group.Relative energies are calculated for three conformers of lithiated diformylimidazolidine, six conformers of lithiated diformylhexahydropyrimidine, and eight conformers of lithiated triformylhexahydro-sym-triazine.For the six-membered rings, conformers with equatorial lithium are always more stable those those with axial lithium.Although equatorial syn-syn conformers (with double O-Li co-ordination) are more stable than equatorial syn-anti, the difference is significantly less than that found between the corresponding syn-anti and (least stable) anti-anti conformers.