139396-15-9

Basic information

• Product Name: (Z)-2-(2,4-Dichloro-5-fluoro-benzoyl)-3-(4-nitro-phenylamino)-acrylic acid ethyl ester
• Synonyms: (Z)-2-(2,4-Dichloro-5-fluoro-benzoyl)-3-(4-nitro-phenylamino)-acrylic acid ethyl ester
• CAS NO: 139396-15-9
• Molecular Weight: 427.216
• Mol File: 139396-15-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (Z)-2-(2,4-Dichloro-5-fluoro-benzoyl)-3-(4-nitro-phenylamino)-acrylic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (Z)-2-(2,4-Dichloro-5-fluoro-benzoyl)-3-(4-nitro-phenylamino)-acrylic acid ethyl ester(139396-15-9)
• EPA Substance Registry System: (Z)-2-(2,4-Dichloro-5-fluoro-benzoyl)-3-(4-nitro-phenylamino)-acrylic acid ethyl ester(139396-15-9)

Safety Data

• Hazardous Substances Data: 139396-15-9(Hazardous Substances Data)

Upstream product

• 86483-51-4 ethyl 2,4-dichloro-5-fluoro-benzoyl-acetate 
• 100-01-6 4-nitro-aniline 
• 104600-41-1 3-(2,4-dichloro-5-fluorophenyl)-3-oxo-2-ethoxymethylenepropanoic acid ethyl ester 
• 86483-52-5 2,4-dichloro-alpha(elhoxymethlene)-5-fluoro-beta-oxo-benzene propanoic acid ethyl ester 

Downstream Products

• 126362-85-4 Ethyl 7-Chloro-6-fluoro-1,4-dihydro-1-(4-nitrophenyl)-4-oxoquinoline-3-carboxylate 
• 139396-27-3 6-Fluoro-7-(3-methyl-piperidin-1-yl)-1-(4-nitro-phenyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid 
• 139396-25-1 6-Fluoro-1-(4-nitro-phenyl)-4-oxo-7-pyrrolidin-1-yl-1,4-dihydro-quinoline-3-carboxylic acid 
• 126362-89-8 6-fluoro-1,4-dihydro-7-(4-methylpiperazin-1-yl)-1-(4-nitrophenyl)-4-oxoquinoline-3-carboxylic acid 
• 126362-88-7 1-(4-nitrophenyl)-6-fluoro-7-(1-piperazinyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid 
• 126362-87-6 7-Chloro-1-(4-nitrophenyl)-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic Acid 

Relevant articles and documents

Synthesis and antibacterial activity of 1-(substituted pyrrolyl)-7- (substituted amino)-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acids

Seventeen quinolone compounds characterized by having a fluorine atom at the 6-position, a substituted amino at the 7-position, and a substituted pyrrolyl at the 1-position were synthesized for the first time. The in vitro antibacterial activities of thes