10390-08-6

Basic information

• Product Name: Propanoic acid, 3-[(4-nitrophenyl)amino]-3-oxo-, ethyl ester
• CAS NO: 10390-08-6
• Molecular Formula: C11H12N2O5
• Molecular Weight: 252.227
• Mol File: 10390-08-6.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Propanoic acid, 3-[(4-nitrophenyl)amino]-3-oxo-, ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Propanoic acid, 3-[(4-nitrophenyl)amino]-3-oxo-, ethyl ester(10390-08-6)
• EPA Substance Registry System: Propanoic acid, 3-[(4-nitrophenyl)amino]-3-oxo-, ethyl ester(10390-08-6)

Safety Data

• Hazardous Substances Data: 10390-08-6(Hazardous Substances Data)

Upstream product

• 100-01-6 4-nitro-aniline 
• 105-53-3 diethyl malonate 
• 14212-59-0 3,3-Diethoxy-acrylsaeure-(4-nitro-anilid) 
• 100-28-7 4-Nitrophenyl isocyanate 
• 623-73-4 diazoacetic acid ethyl ester 
• 201230-82-2 carbon monoxide 
• 1010117-23-3 diethyl 2-nitro-3-oxopentanedioate 

Downstream Products

• 142917-13-3 N-(4-nitro-phenyl)-malonamide 
• 79612-83-2 3,3-Bis-methylsulfanyl-2-(4-nitro-phenylcarbamoyl)-acrylic acid ethyl ester 
• 861357-07-5 N-(4-amino-phenyl)-malonamide 
• 437708-76-4 4-chloro-6-nitro-2-piperazin-1-yl-quinoline 
• 437708-86-6 2,4-dibromo-6-nitroquinoline 
• 143954-73-8 4-Bromo-6-nitro-2-piperazin-1-yl-quinoline 
• 408523-59-1 2,4-dichloro-6-nitroquinoline 
• 264260-06-2 4-hydroxy-6-nitroquinolin-2(1H)-one 
• 121222-79-5 3-hydrazinyl-N-(4-nitrophenyl)-3-oxo-propanamide 
• 65051-10-7 4-Aminophenylcarbamoylessigsaeureethylester 

Relevant articles and documents

Syntheses and binding affinities of 6-nitroquipazine analogues for serotonin transporter. Part 2: 4-Substituted 6-nitroquipazines

Eleven 4-substituted derivatives of 6-nitroquipazine were synthesized and evaluated for their abilities to displace [3H]citalopram binding to the rat cortical synaptic membranes. Among them, 4-chloro-6-nitroquipazine was shown to possess the hi

Design, synthesis and molecular docking of substituted 3-hydrazinyl-3-oxo-propanamides as anti-tubercular agents

Based on the anti-mycobacterial activity of various acid hydrazides, a series of substituted 3-hydrazinyl-3-oxo-propanamides has been designed. The target compounds have been synthesized from diethylmalonate using substituted amines and hydrazine hydrate

Carbene radicals in cobalt(II)-porphyrin-catalysed carbene carbonylation reactions; A catalytic approach to ketenes

One-pot radicals: Cobalt(III)-carbene radicals, generated by metallo-radical activation of diazo compounds and N-tosylhydrazone sodium salts with cobalt(II) complexes of porphyrins, readily undergo radical addition to carbon monoxide, allowing the catalytic production of ketenes. These ketenes subsequently react with various amines, alcohols and imines in one-pot tandem transformations to produce differently substituted amides, esters and β-lactams in good isolated yields. Copyright