95192-60-2 Usage
Uses
Used in Pharmaceutical Industry:
2-BROMO-4,6-DINITROBENZOIC ACID is used as an intermediate in the synthesis of various pharmaceuticals for its ability to contribute to the development of new medications and organic compounds.
Used in Dye and Pigment Industry:
2-BROMO-4,6-DINITROBENZOIC ACID is used as a building block in the creation of dyes and pigments, providing a foundation for the production of various organic substances.
Used in Agrochemical and Pesticide Industry:
2-BROMO-4,6-DINITROBENZOIC ACID is used in the field of agrochemicals and pesticides, indicating its potential applications in these sectors.
Used in Research and Development:
2-BROMO-4,6-DINITROBENZOIC ACID is used in research and development for its contribution to the discovery and formulation of new drugs and medications.
It is crucial to handle 2-BROMO-4,6-DINITROBENZOIC ACID with care due to its toxic nature and potential to cause skin and eye irritation.
Check Digit Verification of cas no
The CAS Registry Mumber 95192-60-2 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, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 95192-60:
(7*9)+(6*5)+(5*1)+(4*9)+(3*2)+(2*6)+(1*0)=152
152 % 10 = 2
So 95192-60-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H3BrN2O6/c8-4-1-3(9(13)14)2-5(10(15)16)6(4)7(11)12/h1-2H,(H,11,12)
95192-60-2Relevant academic research and scientific papers
Substituent Effects on the Decarboxylation of Dinitrobenzoate Ions, Representative Aromatic SE1 Reactions
Segura, Pascual,Bunnett, Joseph F.,Villanova, Laura
, p. 1041 - 1045 (2007/10/02)
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.
