95192-56-6 Usage
Description
4-BROMO-2,6-DINITROBENZOIC ACID is a chemical compound with the molecular formula C7H3BrN2O6, which is a derivative of benzoic acid featuring two nitro and one bromo substituents. 4-BROMO-2,6-DINITROBENZOIC ACID is known for its potential applications in various fields due to its unique chemical structure and properties.
Uses
Used in Organic Synthesis:
4-BROMO-2,6-DINITROBENZOIC ACID is used as a building block in organic synthesis for the creation of complex organic molecules. Its presence of nitro and bromo groups allows for versatile chemical reactions, making it a valuable component in the synthesis of various compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-BROMO-2,6-DINITROBENZOIC ACID is used as a reagent in the preparation of different pharmaceutical compounds. Its unique structure contributes to the development of new drugs with potential therapeutic effects.
Used in Agrochemical Industry:
4-BROMO-2,6-DINITROBENZOIC ACID is also utilized in the agrochemical sector for the production of various agrochemical compounds. Its role in this industry is crucial for the development of effective pesticides and other agricultural chemicals.
Used in Dye and Pigment Production:
4-BROMO-2,6-DINITROBENZOIC ACID has potential applications in the dye and pigment industry, where it can be used to create a range of colors for various applications, from textiles to printing inks.
Used in Electronic Materials Manufacturing:
4-BROMO-2,6-DINITROBENZOIC ACID has been studied for its potential use in the manufacturing of electronic materials, where its chemical properties may contribute to the development of advanced electronic components.
Used in Biological Research:
4-BROMO-2,6-DINITROBENZOIC ACID has been studied for its potential biological activities, including anti-inflammatory and anti-cancer properties. This research could lead to the development of new therapeutic agents for the treatment of various diseases.
Check Digit Verification of cas no
The CAS Registry Mumber 95192-56-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,5,1,9 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 95192-56:
(7*9)+(6*5)+(5*1)+(4*9)+(3*2)+(2*5)+(1*6)=156
156 % 10 = 6
So 95192-56-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H3BrN2O6/c8-3-1-4(9(13)14)6(7(11)12)5(2-3)10(15)16/h1-2H,(H,11,12)
95192-56-6Relevant articles and documents
Substituent Effects on the Decarboxylation of Dinitrobenzoate Ions, Representative Aromatic SE1 Reactions
Segura, Pascual,Bunnett, Joseph F.,Villanova, Laura
, p. 1041 - 1045 (1985)
Kinetics of decarboxylation, in water solution, of several 4-substituted 2,6-dinitrobenzoic and 2-substituted 4,6-dinitrobenzoic acids were determined, at several temperatures.The reactions are first order at the low concentrations employed, at which the acids are fully dissociated.Decarboxylation is accelerated by electron-attracting substituents; the Hammett ρ for the effects of 4-substituents is about +2.6.All the decarboxylations involve large positive enthalpies and entropies of activation.The solvent kinetic isotope effect (D2O/H2O) is not significantly different from unity.The data support a mechanism where in the substituted benzoate ion loses CO2 in the rate-determining step, forming a substituted aryl anion, which is then rapidly hydronated by the solvent.In the case of 2-methoxy-4,6-dinitrobenzoate ion, reaction occured with strikingly different activation parameters.
