95192-58-8 Usage
Uses
Used in Pharmaceutical Industry:
2,6-DINITRO-4-IODOBENZOIC ACID is used as a chemical intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs and medicinal compounds. Its unique chemical properties make it a valuable component in the creation of therapeutic agents.
Used in Dye and Pigment Industry:
In the dye and pigment industry, 2,6-DINITRO-4-IODOBENZOIC ACID is utilized in the production of dyes and pigments, providing colorants for a wide range of applications, including textiles, plastics, and printing inks.
Used in Agrochemical Industry:
2,6-DINITRO-4-IODOBENZOIC ACID is employed in the agrochemical sector for the development of various products, such as herbicides, pesticides, and other agricultural chemicals, which are essential for crop protection and enhancement of agricultural yields.
Check Digit Verification of cas no
The CAS Registry Mumber 95192-58-8 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 8 respectively.
Calculate Digit Verification of CAS Registry Number 95192-58:
(7*9)+(6*5)+(5*1)+(4*9)+(3*2)+(2*5)+(1*8)=158
158 % 10 = 8
So 95192-58-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H3IN2O6/c8-3-1-4(9(13)14)6(7(11)12)5(2-3)10(15)16/h1-2H,(H,11,12)
95192-58-8Relevant 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.
