19013-22-0

Basic information

• Product Name: ethyl 4-hydroxy-3,5-dinitrobenzoate
• CAS NO: 19013-22-0
• Molecular Formula: C₉H₈N₂O₇
• Molecular Weight: 256.169
• Mol File: 19013-22-0.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 344.6°C at 760 mmHg
• Flash Point: 162.2°C
• Density: 1.543g/cm³
• Vapor Pressure: 3.27E-05mmHg at 25°C
• Refractive Index: 1.611
• CAS DataBase Reference: ethyl 4-hydroxy-3,5-dinitrobenzoate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 4-hydroxy-3,5-dinitrobenzoate(19013-22-0)
• EPA Substance Registry System: ethyl 4-hydroxy-3,5-dinitrobenzoate(19013-22-0)

Safety Data

• Hazardous Substances Data: 19013-22-0(Hazardous Substances Data)

Upstream product

• 120-47-8 Ethyl 4-hydroxybenzoate 
• 141-97-9 ethyl acetoacetate 
• 74197-39-0 3,5-dinitro-1-(2-pyridyl)-4-pyridone 
• 7697-37-2 nitric acid 
• 4334-88-7 p-ethoxycarbonylphenylboronic acid 
• 99-96-7 4-hydroxy-benzoic acid 
• 860698-40-4 4-ethoxy-3,5-dinitro-benzoic acid ethyl ester 
• 85365-92-0 3,5-dinitro-4-methoxybenzoic acid 
• 7221-27-4 4-amino-3,5-dinitrobenzoic acid 
• 7647-01-0 hydrogenchloride 
• 64-17-5 ethanol 
• 76520-25-7 3,5-dinitro-1-(6-methyl-2-pyridyl)-4-pyridone 
• 76520-26-8 3,5-dinitro-1-(4-pyridyl)-4-pyridone 
• 19013-10-6 ethyl 4-hydroxy-3-nitrobenzoate 

Downstream Products

• 2379-09-1 4-<4-Benzoyloxy-phenoxy>-3.5-dijod-benzoesaeure-aethylester 
• 1838-55-7 4-(4-hydroxy-phenoxy)-3,5-diiodo-benzoic acid 
• 106883-46-9 4-(2-hydroxy-anilino)-3,5-dinitro-benzoic acid ethyl ester 
• 52532-53-3 4-anilino-3,5-dinitro-benzoic acid ethyl ester 
• 2621-51-4 4-<4-Benzoyloxy-phenoxy>-3.5-dinitro-benzoesaeure-aethylester 
• 19649-81-1 1-chloro-2,6-dinitro-4-carboethoxybenzene 

Relevant articles and documents

Visible-Light-Induced Radical Polynitration of Arylboronic Acids: Synthesis of Polynitrophenols

We report a visible light-assisted one-pot method for the synthesis of polynitrophenols through radical tandem hydroxylation and nitration of arylboronic acids by utilizing copper(II) nitrate tri-nitydrate as the nitro source. This method features mild conditions, a simple procedure, and good functional group tolerance. Compared to conventional methods, this work provides a straightforward approach for the polynitration of aromatic compounds.