1100817-23-9

Basic information

• Product Name: ethyl 1,5-dimethyl-3-oxido-1H-imidazole-4-carboxylate
• Synonyms: ethyl 1,5-dimethyl-3-oxido-1H-imidazole-4-carboxylate
• CAS NO: 1100817-23-9
• Molecular Weight: 184.195
• Mol File: 1100817-23-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: ethyl 1,5-dimethyl-3-oxido-1H-imidazole-4-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 1,5-dimethyl-3-oxido-1H-imidazole-4-carboxylate(1100817-23-9)
• EPA Substance Registry System: ethyl 1,5-dimethyl-3-oxido-1H-imidazole-4-carboxylate(1100817-23-9)

Safety Data

• Hazardous Substances Data: 1100817-23-9(Hazardous Substances Data)

Upstream product

• 1761-67-7 N-methylmethanimine 
• 5408-04-8 ethyl 2-hydroxyimino-3-oxobutanoate 

Downstream Products

• 74531-82-1 ethyl 1,5-dimethyl-1H-imidazole-4-carboxylate 
• 1370588-29-6 4-butyl-5-(1,5-dimethyl-3-oxido-1H-imidazol-4-yl)-2,4-dihydro-3H-1,2,4-triazole-3-thione 
• 1370588-28-5 5-(1,5-dimethyl-3-oxido-1H-imidazol-4-yl)-2,4-dihydro-4-phenyl-3H-1,2,4-triazole-3-thione 
• 1370588-21-8 N-butyl-2-[(1,5-dimethyl-3-oxido-1H-imidazol-4-yl)carbonyl]hydrazinecarbothioamide 
• 1370588-20-7 2-[(1,5-dimethyl-3-oxido-1H-imidazol-4-yl)carbonyl]-N-phenylhydrazinecarbothioamide 
• 1370588-19-4 2-[(1,5-dimethyl-3-oxido-1H-imidazol-4-yl)carbonyl]-N-methylhydrazinecarbothioamide 
• 1256814-09-1 N-cyclohexyl-1,5-dimethyl-3-oxido-1H-imidazole-4-carboxamide 
• 1256814-21-7 N-[(1-(4-methoxyphenyl)-1H-1,2,3-triazol-4-yl)methyl]-1,5-dimethyl-3-oxido-1H-imidazole-4-carboxamide 
• 1256814-20-6 N-methyl-2-(4-fluorophenyl)-1,5-dimethyl-3-oxido-1H-imidazole-4-carboxamide 
• 1307308-66-2 ethyl 2-methoxycarbonylmethyl-1,5-dimethyl-1H-imidazole-4-carboxylate 

Relevant articles and documents

Synthesis and evaluation of antimicrobial activity of hydrazones derived from 3-oxido-1H-imidazole-4-carbohydrazides

In this work we reported the synthesis and evaluation of in vitro antimicrobial activities of hydrazones 6 obtained from 3-oxido-1H-imidazole-4- carbohydrazides 4. All new compounds were characterized by spectroscopic methods. Hydrazones 6 were tested for their in vitro antimicrobial activity against four Gram-positive and four Gram-negative strains of bacteria as well as one fungal species. Three of the tested compounds appeared to be promising agents against reference strains of Escherichia coli, Staphylococcus aureus and Staphylococcus epidermidis. They were also tested against twelve clinical isolates of S. aureus and their cytotoxic effect on murine fibroblasts and HeLa human tumor cell line was determined.