610-28-6 Usage
Uses
Used in Chemical Synthesis:
2,5-Dinitrobenzoic acid is used as a key intermediate in the synthesis of various organic compounds and pharmaceuticals. Its reactivity and functional groups make it a versatile building block for creating a wide range of molecules with diverse applications.
Used in Analytical Chemistry:
In analytical chemistry, 2,5-dinitrobenzoic acid is employed as a derivatizing agent for the detection and quantification of certain organic compounds. Its ability to form stable derivatives with specific functional groups allows for improved detection and analysis of target molecules.
Used in Material Science:
2,5-Dinitrobenzoic acid can be utilized in the development of new materials with unique properties. Its incorporation into polymers or other materials can lead to enhanced thermal stability, mechanical strength, or other desirable characteristics.
Used in Research and Development:
The study of 2,5-dinitrobenzoic acid's proton, deuteron, and proton spin-lattice relaxation times using Schr?dinger wave equation contributes to the understanding of its molecular structure and behavior. This knowledge can be applied to further research and development in various scientific fields, including chemistry, physics, and materials science.
Purification Methods
Crystallise the acid from distilled H2O. Dry it in a vacuum desiccator. [Beilstein 9 II 279, 9 III 1778, 9 IV 1241.]
Check Digit Verification of cas no
The CAS Registry Mumber 610-28-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,1 and 0 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 610-28:
(5*6)+(4*1)+(3*0)+(2*2)+(1*8)=46
46 % 10 = 6
So 610-28-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H4N2O6/c10-7(11)5-3-4(8(12)13)1-2-6(5)9(14)15/h1-3H,(H,10,11)/p-1
610-28-6Relevant academic research and scientific papers
PROCESS FOR PREPARING SUBSTITUTED AROMATIC CARBOXYLIC ACIDS
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Page/Page column 3, (2010/09/17)
A process for preparing an aromatic carboxylic acid having a heteroatom containing substituent is provided that includes reaction in a vessel of an aromatic precursor having an aromatic core with at least one heteroatom containing substituent and at least one hydrogen extending from the core, with a haloacetonitrile under reaction conditions to form an aromatic acetonitrile with an acetonitrile moiety. The aromatic acetonitrile is exposed to an oxidizing agent under conditions to convert the acetonitrile moiety to a carboxylic acid group to prepare the aromatic carboxylic acid having the heteroatom containing substituent.
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
Moodie, Roy B.,Sanderson, Andrew J.,Willmer, Richard
, p. 645 - 650 (2007/10/02)
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.
Xi:Irritant;
