77889-24-8

Basic information

• Product Name: 1-benzyl-2-phenethyl-4,5-dihydro-1H-imidazole
• Synonyms: 1-benzyl-2-phenethyl-4,5-dihydro-1H-imidazole
• CAS NO: 77889-24-8
• Molecular Weight: 264.37
• Mol File: 77889-24-8.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-benzyl-2-phenethyl-4,5-dihydro-1H-imidazole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-benzyl-2-phenethyl-4,5-dihydro-1H-imidazole(77889-24-8)
• EPA Substance Registry System: 1-benzyl-2-phenethyl-4,5-dihydro-1H-imidazole(77889-24-8)

Safety Data

• Hazardous Substances Data: 77889-24-8(Hazardous Substances Data)

Upstream product

• 103-25-3 3-phenylpropanoic acid methyl ester 
• 4152-09-4 N-benzylethylenediamine 
• 104-53-0 3-phenyl-propionaldehyde 
• 100-39-0 benzyl bromide 
• 120671-12-7 1-benzyl-2-(ethoxycarbonylmethylene)-2,3,4,5-tetrahydroimidazole 
• 6096-36-2 1-benzyl-2-methyl-4,5-dihydro-1H-imidazole 

Relevant articles and documents

A Novel Class of Dopamine D4Receptor Ligands Bearing an Imidazoline Nucleus

Over the years, the 2-substituted imidazoline nucleus has been demonstrated to be a bioversatile structural motif. In this study, novel imidazoline derivatives bearing a 3- and/or 4-hydroxy- or methoxy-substituted phenyl ring, linked by an ethylene bridge

Alkylation of an imidazolidine enaminoester: A new sequence for the c(α)-alkylation of 4,5-dihydroimidazoles

1-Benzyl-2-(ethoxycarbonyllmethylene)-2,3,4,5-tetrahydroimidazole undergoes preferred C-alkylation with halogenonakanes, dihalogenoalkanes and epoxides: subsequent removal of of the ethoxycarbonyl group provides a new route to 2-alkyl-4,5-dihydroimidazoles. 1,3-Dihalogenoalkanes afford imidazo[1,2-a]pyridines via C,N-dialkylation.

Imidazolines in synthesis, I: lithio imidazolines formation and C-alkylation

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