126362-89-8

Basic information

• Product Name: 3-Quinolinecarboxylic acid, 6-fluoro-1,4-dihydro-7-(4-methyl-1-piperazinyl)-1-(4-nitrophenyl)-4-oxo-
• CAS NO: 126362-89-8
• Molecular Formula: C21H19FN4O5
• Molecular Weight: 426.404
• Mol File: 126362-89-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 3-Quinolinecarboxylic acid, 6-fluoro-1,4-dihydro-7-(4-methyl-1-piperazinyl)-1-(4-nitrophenyl)-4-oxo-(CAS DataBase Reference)
• NIST Chemistry Reference: 3-Quinolinecarboxylic acid, 6-fluoro-1,4-dihydro-7-(4-methyl-1-piperazinyl)-1-(4-nitrophenyl)-4-oxo-(126362-89-8)
• EPA Substance Registry System: 3-Quinolinecarboxylic acid, 6-fluoro-1,4-dihydro-7-(4-methyl-1-piperazinyl)-1-(4-nitrophenyl)-4-oxo-(126362-89-8)

Safety Data

• Hazardous Substances Data: 126362-89-8(Hazardous Substances Data)

Upstream product

• 109-01-3 1-methyl-piperazine 
• 126362-87-6 7-Chloro-1-(4-nitrophenyl)-6-fluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic Acid 
• 631898-47-0 6,7-difluoro-1,4-dihydro-7-(4-methylpiperazin-1-yl)-1-(4-nitrophenyl)-4-oxoquinoline-3-carboxylic acid 
• 350-46-9 4-Fluoronitrobenzene 
• 75073-15-3 ethyl 7-chloro-6-fluoro-4-oxo-1,4-dihydroquinoline 3-carboxylate 
• 139396-15-9 (Z)-2-(2,4-Dichloro-5-fluoro-benzoyl)-3-(4-nitro-phenylamino)-acrylic acid ethyl ester 
• 126362-85-4 Ethyl 7-Chloro-6-fluoro-1,4-dihydro-1-(4-nitrophenyl)-4-oxoquinoline-3-carboxylate 
• 86483-51-4 ethyl 2,4-dichloro-5-fluoro-benzoyl-acetate 
• 100-01-6 4-nitro-aniline 

Downstream Products

• 102855-98-1 1-(4-aminophenyl)-6-fluoro-1,4-dihydro-7-(4-methylpiperazin-1-yl)-4-oxoquinoline-3-carboxylic acid 

Relevant articles and documents

Synthesis and antimycobacterial evaluation of certain fluoroquinolone derivatives

A number of fluoroquinolone derivatives were synthesized and evaluated for antimycobacterial activity. Preliminary results are (1) for 1-aryl fluoroquinolones, 1-(4-nitrophenyl) derivatives were inactive while their 1-(2-fluoro-4-nitrophenyl) counterparts

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