150093-92-8

Basic information

• Product Name: 2H-Imidazole-2-thione, 1,3-dihydro-4-methyl-5-phenyl-1-(phenylamino)-
• Synonyms: 2H-Imidazole-2-thione, 1,3-dihydro-4-methyl-5-phenyl-1-(phenylamino)-
• CAS NO: 150093-92-8
• Molecular Formula: C₁₆H₁₅N₃S
• Molecular Weight: 281.38
• Mol File: 150093-92-8.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2H-Imidazole-2-thione, 1,3-dihydro-4-methyl-5-phenyl-1-(phenylamino)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2H-Imidazole-2-thione, 1,3-dihydro-4-methyl-5-phenyl-1-(phenylamino)-(150093-92-8)
• EPA Substance Registry System: 2H-Imidazole-2-thione, 1,3-dihydro-4-methyl-5-phenyl-1-(phenylamino)-(150093-92-8)

Safety Data

• Hazardous Substances Data: 150093-92-8(Hazardous Substances Data)

Upstream product

• 93-55-0 1-phenyl-propan-1-one 
• 333-20-0 potassium thioacyanate 
• 2114-00-3 2-bromo-1-phenyl-1-propanone 
• 100-63-0 phenylhydrazine 
• 85217-09-0 C₂₁H₂₂N₄ 

Downstream Products

• 1435872-23-3 2-cyclohexylimino-2,3-dihydro-3,5-diphenyl-6-methyl-imidazo[2,1-b][1,3,4]thiadiazole 
• 1435872-25-5 2,3-dihydro-2-(tert-butylimino)-3,5-diphenyl-6-methyl-imidazo[2,1-b][1,3,4]thiadiazole 
• 1207379-20-1 dimethyl (2Z)-2-[(1-anilino-4-methyl-5-phenyl-1H-imidazol-2-yl)thio]but-2-enedioate 
• 1207379-11-0 (2E)-2-[anilino(methoxycarbonyl)methylene]-5-methyl-6-phenylimidazo[2,1-b][1,3]thiazol-3(2H)-one 

Relevant articles and documents

Addition Products of Hydrazine Derivatives to Azo-Alkenes, Part V: The Reaction of α-(1-Phenylhydrazino)alkanone Phenylhydrazones with Acids and Acid Derivatives

The bifunctional title compounds 2 react with acylating, carbamoylating and sulfonylating reagents mostly at the primary amino group of the hydrazine function.Both functional groups of 2 are attacked by N,N'-carbonyldiimidazole converting it into 1H-1,2,4

Direct synthetic approach to N-substituted 1-amino-2,3-dihydro-1H-imidazole-2-thiones

In an efficient one-pot procedure, the title compounds (8) were obtained by the reaction of α-halo ketones (1) with potassium thiocyanate and monosubstituted hydrazines (3). The reaction is considered to proceed via the formation of azo-alkenes (5) and th