15147-64-5

Basic information

• Product Name: 2,3-DINITROBENZOIC ACID
• Synonyms: 2,3-DINITROBENZOIC ACID;NSC 137840
• CAS NO: 15147-64-5
• Molecular Formula: C₇H₄N₂O₆
• Molecular Weight: 212.12
• Product Categories: Aromatic Carboxylic Acids, Amides, Anilides, Anhydrides & Salts;pharmacetical
• Mol File: 15147-64-5.mol

Chemical Properties

• Boiling Point: 440.2 °C at 760 mmHg
• Flash Point: 199.9 °C
• Appearance: /
• Density: 1.688
• Vapor Pressure: 1.58E-08mmHg at 25°C
• Refractive Index: 1.658
• PKA: pK1:1.85 (25°C)
• CAS DataBase Reference: 2,3-DINITROBENZOIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3-DINITROBENZOIC ACID(15147-64-5)
• EPA Substance Registry System: 2,3-DINITROBENZOIC ACID(15147-64-5)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 15147-64-5(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
2,3-Dinitrobenzoic acid is utilized as a reagent in organic synthesis for its ability to facilitate the formation of desired organic compounds through chemical reactions.
Used as a Precursor in Dye and Pharmaceutical Production:
In the dye and pharmaceutical industries, 2,3-Dinitrobenzoic acid serves as a precursor, meaning it is a starting material that is chemically transformed into the final product.
Used in Corrosion Inhibition:
2,3-Dinitrobenzoic acid has been studied for its potential as a corrosion inhibitor, indicating its use in protecting materials from the damaging effects of corrosion.
Used as an Anti-Microbial Agent:
2,3-Dinitrobenzoic acid has also been investigated for its anti-microbial properties, suggesting its application in controlling or preventing microbial growth in various settings.
It is crucial to handle 2,3-Dinitrobenzoic acid with caution due to its toxic and potentially hazardous nature, ensuring safety in its application across different industries.

InChI:InChI=1/C7H4N2O6/c10-7(11)4-2-1-3-5(8(12)13)6(4)9(14)15/h1-3H,(H,10,11)

Upstream product

• 607-35-2 8-nitroquinoline 
• 602-01-7 1-methyl-2,3-dinitrobenzene 
• 13985-57-4 1-ethyl-2,3-dinitrobenzene 
• 552-16-9 ortho-nitrobenzoic acid 
• 7697-37-2 nitric acid 
• 7664-93-9 sulfuric acid 
• 859943-94-5 1,2-dinitro-3-propyl-benzene 
• 570-24-1 2-Methyl-6-nitroaniline 
• 99-08-1 1-methyl-3-nitrobenzene 
• 392303-95-6 acetic acid-(4-ethyl-2,3-dinitro-anilide) 
• 335201-54-2 4-ethyl-2,3-dinitrobenzeneamine 
• 5805-89-0 N-(4-ethyl-3-nitrophenyl)acetamide 

Downstream Products

• 19613-80-0 di-nitrophenylcarboxamide 
• 711007-44-2 2,3-diaminobenzamide 
• 858136-29-5 2,3-dinitrobenzylalcohol 
• 603-81-6 2,3-diaminobenzoic acid 
• 73406-19-6 2-Benzylthio-3-nitrobenzoesaeure 

Relevant articles and documents

A green, reusable and highly efficient solid acid catalyst for the oxidation of aldehydes to the corresponding carboxylic acids using H 2O2 and KMnO4:H5PV 2Mo10O40 (10-molybdo-2-vanadophosphoric heteropolyacid)

H5PV2Mo10O40-catalyzed oxidation of aromatic aldehydes to the corresponding carboxylic acids using hydrogen peroxide and KMnO4 as oxidants under mild conditions is reported. This system provides an efficient, convenient and practical method for the oxidation of aromatic aldehydes. In this work, differences between Keggin and Well-Dawson type polyoxometalates are addressed in term of relative stability, hardness and acidity.

Electrophilic Aromatic Substitution. Part 37. Products of Aromatic Nitrations of some Chloronitrobenzenes and Substituted Benzoic Acids in Solutions of Dinitrogen Pentaoxide and of Nitronium Salts in Nitric Acid

Yields of aromatic products of nitration in nitric acid solutions containing dinitrogen pentaoxide or nitronium salt have been determined.Evidence for the intrusion of a mechanism other than the normal nitronium ion one comes from comparison of products in the two media and from the observation of 15N NMR CIDPN effects.The additional mechanism operative with some substrates in concentrated solutions of dinitrogen pentaoxide is postulated to be one in which reversible addition of the NO3 radical is followed by combination with NO2.Dienes produced in this way can give aromatic nitroproducts by elimination of nitric acid.Nitrodecarboxylation of substituted benzoic acids occurs by a radical process.