166593-11-9

Basic information

• Product Name: 1,3-dihydro-1,5-dimethyl-4-phenyl-2H-imidazole-2-thione
• Synonyms: 1,3-dihydro-1,5-dimethyl-4-phenyl-2H-imidazole-2-thione
• CAS NO: 166593-11-9
• Molecular Weight: 204.296
• Mol File: 166593-11-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,3-dihydro-1,5-dimethyl-4-phenyl-2H-imidazole-2-thione(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3-dihydro-1,5-dimethyl-4-phenyl-2H-imidazole-2-thione(166593-11-9)
• EPA Substance Registry System: 1,3-dihydro-1,5-dimethyl-4-phenyl-2H-imidazole-2-thione(166593-11-9)

Safety Data

• Hazardous Substances Data: 166593-11-9(Hazardous Substances Data)

Upstream product

• 25355-34-4 1-phenyl-propane-1,2-dione 1-oxime 
• 215675-50-6 1,5-dimethyl-4-phenylimidazole 3-oxide 
• 333-20-0 potassium thioacyanate 
• 49656-78-2 2-methylamino-1-phenyl-1-propanone hydrochloride 

Downstream Products

• 1138238-22-8 (Z)-2-[(1,5-dimethyl-4-phenyl-1H-imidazol-2-yl)sulfanyl]but-2-enedioic acid dimethyl ester 
• 1449684-44-9 2-{[(1,5-dimethyl-4-phenyl-1H-imidazol-2-yl)sulfanyl]acetyl}-N-(4-fluorophenyl)hydrazinecarboselenoamide 
• 1449684-43-8 2-{[ (1,5-dimethyl-4-phenyl-1H-imidazol-2-yl)sulfanyl]acetyl}-N-(4-methoxyphenyl)hydrazinecarboselenoamide 
• 1449684-49-4 2-[(1,5-dimethyl-4-phenyl-1H-imidazol-2-yl)sulfanyl]acetohydrazide 
• 62576-13-0 1,5-0dimethyl-4-phenyl-1H-imidazole 

Relevant articles and documents

Ambivalent nucleophilicity of 1,4,5-trisubstituted imidazole-2-thiones in reactions with dimethyl acetylenedicarboxylate and phenylisocyanate

The 1,4,5-trisubstitued 2,3-dihydro-1H-imidazole-2-thiones 1 react with electrophilic reagents via the S- or the N(3)-atom. The reaction with dimethyl acetylenedicarboxylate in methanol at room temperature occurs by the nucleophilic addition of the S-atom

Novel imidazoles and hydantoins moderately strained by incorporation with 2-azabicyclo[2.2.1]heptene skeleton

The reactions of 3-acyl-2-azabicyclo[2.2.1]hept-5-enes with phenyl isocyanate, phenyl isothiocyanate, and ethoxycarbonyl isothiocyanate followed by cyclization reactions under basic conditions respectively provided a hydantoin, a thiohydantoin, and a 1,3-