95192-60-2 Usage
General Description
2-Bromo-4,6-dinitrobenzoic acid is a chemical compound with the molecular formula C7H3BrN2O6. It is a yellow crystalline solid that is used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. 2-BROMO-4,6-DINITROBENZOIC ACID is often employed as a building block in the creation of dyes, pigments, and other organic substances. It is also used in the research and development of new drugs and medications. Additionally, it has potential applications in the field of agrochemicals and pesticides. However, it is important to handle this compound with caution, as it is known to be toxic and may 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 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 (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.
