22751-16-2

Basic information

• Product Name: Benzenepropanoic acid, 2-nitro-b-oxo-
• CAS NO: 22751-16-2
• Molecular Formula: C9H7NO5
• Molecular Weight: 209.158
• Mol File: 22751-16-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzenepropanoic acid, 2-nitro-b-oxo-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenepropanoic acid, 2-nitro-b-oxo-(22751-16-2)
• EPA Substance Registry System: Benzenepropanoic acid, 2-nitro-b-oxo-(22751-16-2)

Safety Data

• Hazardous Substances Data: 22751-16-2(Hazardous Substances Data)

Upstream product

• 52119-39-8 ethyl (2-nitrobenzoyl)acetate 
• 610-14-0 2-nitrobenzyl chloride 
• 57206-51-6 2-(2-Nitrobenzoyl)acetessigsaeureethylester 

Downstream Products

• 2503-80-2 4-hydroxy-2-heptylquinoline 
• 482-89-3 1H,1H'-2,2'-Biindolylidene-3,3'-dione 
• 16662-90-1 3-(2-aminophenyl)-3-oxopropanoic acid 
• 52119-39-8 ethyl (2-nitrobenzoyl)acetate 
• 70254-43-2 4-Hydroxy-2-quinolone 
• 577-59-3 2-acetylnitrobenzene 
• 15719-64-9 methylammonium carbonate 
• 551-93-9 2-aminoacetophenone 
• 156489-07-5 Acetic acid 2-[2,7-dichloro-5,8-dihydroxy-4-(2-nitro-phenyl)-quinolin-6-yl]-ethyl ester 
• 156489-06-4 Acetic acid 2-[2,7-dichloro-4-(2-nitro-phenyl)-5,8-dioxo-5,8-dihydro-quinolin-6-yl]-ethyl ester 
• 156488-99-2 N-(5-Methoxy-2,3-dihydro-benzofuran-6-yl)-3-(2-nitro-phenyl)-3-oxo-propionamide 
• 156489-00-8 5-Methoxy-9-(2-nitro-phenyl)-3,6-dihydro-2H-furo[2,3-f]quinolin-7-one 
• 156489-03-1 4,7-Dichloro-9-(2-nitro-phenyl)-2,3-dihydro-furo[2,3-f]quinolin-5-ol 
• 156489-04-2 2,7-Dichloro-6-(2-hydroxy-ethyl)-4-(2-nitro-phenyl)-quinoline-5,8-dione 

Relevant articles and documents

Engineered Biosynthesis of Fungal 4-Quinolone Natural Products

Quinolone-containing natural products are widely found in bacteria, fungi, and plants. The fungal quinolactacins, which are N-methyl-4-quinolones, display a wide spectrum of biological activities. Here we uncovered a concise nonribosomal peptide synthetase pathway involved in quinolactacin A biosynthesis from Penicillium by using heterologous reconstitution and in vitro enzymatic synthesis. The N-desmethyl analog of quinolactacin A was accessed through the construction of a hybrid bacterial and fungi pathway in the heterologous host.

NOVEL ARYL HYDROCARBON RECEPTOR LIGANDS DERIVED FROM KYNURENINE

The present invention relates to novel compounds which are aryl hydrocarbon receptor (AHR) ligands and uses thereof.

The end of an old hypothesis: The pseudomonas signaling molecules 4-hydroxy-2-alkylquinolines derive from fatty acids, not 3-ketofatty acids

Summary Groups of pathogenic bacteria use diffusible signals to regulate their virulence in a concerted manner. Pseudomonas aeruginosa uses 4-hydroxy-2-alkylquinolines (HAQs), including 4-hydroxy-2-heptylquinoline (HHQ) and 3,4-dihydroxy-2-heptylquinoline