89002-63-1

Usage

Class

Imidazole

Substituent

4,4-dimethyl-2-phenyl

Applications

Drug development, specialty polymers, organic compound synthesis

Properties

Enhanced stability and reactivity

Upstream product

• 112100-29-5 1,5-dihydro-5-methoxy-4,4-dimethyl-2-phenyl-4H-imidazole 
• 89002-69-7 1-(2-methylprop-1-enyl)-5-phenyltetrazole 
• 112081-41-1 N-(2-Methyl-propenyl)-benzimidoyl chloride 
• 55-21-0 benzamide 
• 5202-81-3 N-(2-methyl-1-propen-1-yl)benzamide 

Downstream Products

• 112081-44-4 1,5-dihydro-4,4,5-trimethyl-2-phenyl-4H-imidazole 
• 13682-20-7 4,5-dimethyl-2-phenyl-1H-imidazole 
• 90859-31-7 1,5-dihydro-5-hydroxy-4,4-dimethyl-2-phenyl-4H-imidazole 
• 89002-68-6 4,4,5-trimethyl-2-phenyl-4H-imidazole 
• 112100-29-5 1,5-dihydro-5-methoxy-4,4-dimethyl-2-phenyl-4H-imidazole 

Relevant academic research and scientific papers

Synthesis and Properties of 4H-Imidazoles

The photolysis of 1-vinyltetrazoles to give 1H-imidazoles is extended to the synthesis of isolable nonaromatic 4H-imidazoles when the vinyl group is terminally disubstituted.Thus photolysis of the 2-phenyltetrazole (7a), prepared from isobutyraldehyde, at

Synthesis and Properties of 4H-Imidazoles

Photolysis of alkenyltetrazoles (1) provides the first rational route to simple 4H-imidazoles (2); when unsubstituted at C-5 these are highly reactive towards nucleophiles and rearrange rapidly to the aromatic 1H-imidazoles on heating.