1201-15-6

Basic information

• Product Name: 2H-Imidazol-2-one, 1,3-dihydro-1-methyl-3-phenyl-
• CAS NO: 1201-15-6
• Molecular Formula: C10H10N2O
• Molecular Weight: 174.202
• Mol File: 1201-15-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2H-Imidazol-2-one, 1,3-dihydro-1-methyl-3-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-Imidazol-2-one, 1,3-dihydro-1-methyl-3-phenyl-(1201-15-6)
• EPA Substance Registry System: 2H-Imidazol-2-one, 1,3-dihydro-1-methyl-3-phenyl-(1201-15-6)

Safety Data

• Hazardous Substances Data: 1201-15-6(Hazardous Substances Data)

Upstream product

• 928729-62-8 1-methyl-1-(2,2-dimethoxyethyl)-3-phenylurea 
• 103-71-9 phenyl isocyanate 
• 74-89-5 methylamine 
• 33876-94-7 N-phenyl-1H-imidazole-1-carboxamide 
• 74-88-4 methyl iodide 
• 62-53-3 aniline 
• 53995-05-4 N-Phenylcarbamoylaminoacetaldehyde dimethyl acetal 
• 53995-06-5 1-phenyl-1,3-dihydro-2H-imidazol-2-one 

Downstream Products

• 1095319-49-5 5-(2,4-dihydroxy-3-methylphenyl)-1-methyl-3-phenylimidazolidin-2-one 
• 1095319-50-8 4-(2,3,4-trihydroxy-phenyl)-3-methyl-1-phenylimidazolidin-2-one 
• 16939-00-7 1-phenyl-3,4-dimethylimidazol-2(1H)-one 
• 392691-83-7 4-(3-methyl-2-oxoimidazolidin-1-yl)benzene-1-sulfonyl chloride 

Relevant articles and documents

Nucleophilic Cyclization/Electrophilic Substitution of (2,2-Dialkoxyethyl)ureas: Highly Regioselective Access to Novel 4-(Het)arylimidazolidinones and Benzo[ d[[1,3]diazepinones

Imidazolidin-2-one and 1,3-benzodiazepin-2-one scaffolds are structural motifs of many biologically active compounds. Herein, we report a highly regioselective acid-catalyzed intramolecular nucleophilic cyclization/intermolecular electrophilic substitutio

Reactions of resorcinol derivatives with 1-methyl-3-phenylimidazol-2-one as a new method for the synthesis of 5-arylimidazolidin-2-ones

Substituted imidazolidin-2-ones have been synthesised by the interaction of imidazol-2-one with 2-methylresorcinol and pyrogallol in a chloroform solution in the presence of trifluoroacetic acid.

Efficient solid-phase synthesis of disubstituted 1,3-dihydro-imidazol-2- ones

A bromoacetal linker was used to achieve the synthesis of ureas on a solid support. The resulting ureido acetals were treated with TFA and were converted in an intramolecular cyclization via N-acyliminium ion to disubstituted 1,3-dihydro-imidazol-2-ones.