154371-62-7

Basic information

• Product Name: 1-(benzyloxymethyl)-2-butyl-4,5-diiodoimidazole
• Synonyms: 1-(benzyloxymethyl)-2-butyl-4,5-diiodoimidazole
• CAS NO: 154371-62-7
• Molecular Weight: 496.13
• Mol File: 154371-62-7.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-(benzyloxymethyl)-2-butyl-4,5-diiodoimidazole(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(benzyloxymethyl)-2-butyl-4,5-diiodoimidazole(154371-62-7)
• EPA Substance Registry System: 1-(benzyloxymethyl)-2-butyl-4,5-diiodoimidazole(154371-62-7)

Safety Data

• Hazardous Substances Data: 154371-62-7(Hazardous Substances Data)

Upstream product

• 50790-93-7 2-butyl-1H-imidazole 
• 3587-60-8 Benzyloxymethyl chloride 
• 154371-61-6 2-butyl-4,5-diiodoimidazole 

Downstream Products

• 154371-51-4 1-(benzyloxymethyl)-2-butyl-4-iodoimidazole-5-carboxaldehyde 
• 154371-56-9 2-butyl-5-(t-butyldimethylsilyloxy)methyl-4-iodo-1-<4-(2-cyanophenyl)phenyl>methylimidazole 
• 124750-35-2 2-butyl-5-hydroxymethyl-4-iodo-1-<4-(2-cyanophenyl)phenyl>methyl-imidazole 
• 154371-55-8 2-butyl-4-iodo-1-<4-(2-cyanophenyl)phenyl>methyl-imidazole-5-carbox-aldehyde 
• 154371-54-7 2-butyl-1-(4-carbomethoxybenzyl)-4-iodoimidazole-5-carboxaldehyde 
• 133040-05-8 4-[5-(1-Acetoxy-2-methoxycarbonyl-3-thiophen-2-yl-propyl)-2-butyl-imidazol-1-ylmethyl]-benzoic acid methyl ester 
• 133040-04-7 2-butyl-1-(4-carbomethoxybenzyl)-5-<2-carbomethoxy-1-hydroxy-3-(2-thienyl)propyl>imidazole 
• 133040-06-9 methyl (E)-3-<2-butyl-1-<(4-carbomethoxyphenyl)methyl>imidazol-5-yl>-2-(2-thienylmethyl)-2-propenoate 
• 133040-01-4 eprosartan 
• 133040-03-6 2-n-butyl-1-[(4-carbomethoxyphenyl)methyl]-1H-imidazol-5-carboxaldehyde 

Relevant articles and documents

2-butyl-4-iodoimidazole-5-carboxaldehyde: A versatile intermediate for the synthesis of highly functionalized imidazoles

The facile preparation of 2-butyl-4-iodoimidazole-5-carboxaldehyde 1 is described. The versatility of this intermediate in the synthesis of highly functionalized imidazoles is demonstrated with the synthesis of two potent and selective angiotensin II rece