1040373-81-6

Basic information

• Product Name: 2-hydroxy-1-methyl-2-(3-nitrophenyl)-2,3-dihydro-1H-imidazo[1,2-a]pyrimidin-4-ium bromide
• Synonyms: 2-hydroxy-1-methyl-2-(3-nitrophenyl)-2,3-dihydro-1H-imidazo[1,2-a]pyrimidin-4-ium bromide
• CAS NO: 1040373-81-6
• Molecular Weight: 353.175
• Mol File: 1040373-81-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-hydroxy-1-methyl-2-(3-nitrophenyl)-2,3-dihydro-1H-imidazo[1,2-a]pyrimidin-4-ium bromide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-hydroxy-1-methyl-2-(3-nitrophenyl)-2,3-dihydro-1H-imidazo[1,2-a]pyrimidin-4-ium bromide(1040373-81-6)
• EPA Substance Registry System: 2-hydroxy-1-methyl-2-(3-nitrophenyl)-2,3-dihydro-1H-imidazo[1,2-a]pyrimidin-4-ium bromide(1040373-81-6)

Safety Data

• Hazardous Substances Data: 1040373-81-6(Hazardous Substances Data)

Upstream product

• 931-61-3 N-methylpyrimidin-2-amine 
• 2227-64-7 3'-nitro-2-bromoacetophenone 

Downstream Products

• 1574306-34-5 tert-butyl 4-(3-(furan-2-carboxamido)phenyl)-2-(methylamino)-4,5-dihydro-1H-imidazole-1-carboxylate 
• 1574306-33-4 tert-butyl 4-(3-(1H-indole-2-carboxamido)phenyl)-2-(methylamino)-4,5-dihydro-1H-imidazole-1-carboxylate 
• 1574306-32-3 tert-butyl 4-(3-(1H-pyrrole-2-carboxamido)phenyl)-2-(methylamino)-4,5-dihydro-1H-imidazole-1-carboxylate 
• 1574306-31-2 tert-butyl 4-(3-(1H-indole-2-carboxamido)phenyl)-2-(methylamino)-1H-imidazole-1-carboxylate 
• 1574306-30-1 tert-butyl 4-(3-(furan-2-carboxamido)phenyl)-2-(methylamino)-1H-imidazole-1-carboxylate 
• 1574306-51-6 tert-butyl 4-(3-aminophenyl)-2-(methylamino)-4,5-dihydro-1H-imidazole-1-carboxylate 
• 1574306-50-5 tert-butyl 4-(3-aminophenyl)-2-(methylamino)-1H-imidazole-1-carboxylate 
• 1574306-49-2 tert-butyl 2-(methylamino)-4-(3-nitrophenyl)-1H-imidazole-1-carboxylate 
• 1574306-48-1 2-(methylamino)-4-(3-nitrophenyl)-1H-imidazolium bromide 

Relevant articles and documents

COMPOSITIONS PROVIDING ENHANCED ANTIBACTERIAL ACTIVITY AGAINST GRAM-POSITIVE BACTERIA AND USE THEREOF

A method of inhibiting, reducing growth of or destroying gram positive bacteria comprising contacting the gram positive bacteria with an effective amount of a 2-(substituted-amino)-imidazole compound and with an additional antibacterial compound separatel

Structure-activity relationship of 2-hydroxy-2-aryl-2,3-dihydro-imidazo[1, 2-a]pyrimidinium salts and 2N-substituted 4(5)-aryl-2-amino-1H-imidazoles as inhibitors of biofilm formation by Salmonella Typhimurium and Pseudomonas aeruginosa

A library of 80 1-substituted 2-hydroxy-2-aryl-2,3-dihydro-imidazo[1,2-a] pyrimidinium salts and 54 2N-substituted 4(5)-aryl-2-amino-1H-imidazoles was synthesized and tested for the antagonistic effect against biofilm formation by Salmonella Typhimurium a