55204-24-5

Basic information

• Product Name: 2-amino-4-nitro-benzoic acid ethyl ester
• Synonyms: 2-amino-4-nitro-benzoic acid ethyl ester;Ethyl 2-amino-4-nitrobenzoate
• CAS NO: 55204-24-5
• Molecular Formula: C₉H₁₀N₂O₄
• Molecular Weight: 210.19
• Mol File: 55204-24-5.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-amino-4-nitro-benzoic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-amino-4-nitro-benzoic acid ethyl ester(55204-24-5)
• EPA Substance Registry System: 2-amino-4-nitro-benzoic acid ethyl ester(55204-24-5)

Safety Data

• Hazardous Substances Data: 55204-24-5(Hazardous Substances Data)

Usage

Chemical compound

2-amino-4-nitro-benzoic acid ethyl ester

Physical properties

yellow to orange crystalline powder

Usage

production of pharmaceuticals, dyes, and pigments

Derivative

ester derivative of 2-amino-4-nitrobenzoic acid

Applications

precursor in drug synthesis, production of dyes and pigments

Potential benefits

studied for anti-tumor properties, used in cancer research

Upstream product

• 75-03-6 ethyl iodide 
• 619-17-0 4-Nitroanthranilic acid 
• 64-17-5 ethanol 
• 67-56-1 methanol 
• 87840-67-3 ethyl 2-amino-4-nitrobenzoate 
• 131223-03-5 2-(2,4-dinitrophenyl)-1,1-dicyanoethylene 
• 2879-79-0 N-(2-methyl-5-nitrophenyl)acetamide 
• 951-97-3 2-acetamido-4-nitrobenzoic acid 

Downstream Products

• 26059-83-6 7-Nitro-2-phenyl-1,3-benzoxazin-2-one 
• 90870-56-7 Aethyl-2-methansulfonamido-4-nitrobenzoat 
• 1026488-77-6 2-[3-(2-Iodo-phenyl)-ureido]-4-nitro-benzoic acid ethyl ester 
• 211318-93-3 2-[3-(2-chloro-ethyl)-ureido]-4-nitro-benzoic acid ethyl ester 
• 55204-25-6 2-acetylamino-4-nitro-benzoic acid ethyl ester 
• 194155-27-6 2-[Bis[(1,1-dimethylethoxy)-carbonyl]amino]-4-nitro-benzoic acid ethyl ester 
• 954097-41-7 C₄₆H₅₈N₆O₁₂ 

Relevant articles and documents

Chromoionophore and method of determining potassium ions

The invention relates to methods of determining potassium ions in a sample, wherein the ions are contacted with a compound having chromophoric moiety and an ionophoric moiety, where the ionophoric moiety interacts with the potassium ions present in the sample, resulting in the chromophoric moiety changing its radiation absorption properties in the ultraviolet and visible regions of the spectrum. For example, a change in an intensity of an absorption maximum is measured and the ion concentration is determined accordingly.

A Convenient One-Step Synthesis of Ethyl 2-amino-4-nitrobenzoate and Analogues by Rearrangement of 2,4-Dinitrobenzylidenemalonates

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