95192-58-8 Usage
General Description
2,6-DINITRO-4-IODOBENZOIC ACID is a chemical compound with the molecular formula C7H4N2O6Cl and a molar mass of 296.47 g/mol. It is a yellow crystalline solid that is commonly used as an intermediate in the synthesis of various pharmaceuticals and organic compounds. 2,6-DINITRO-4-IODOBENZOIC ACID is also utilized in the production of dyes, pigments, and agrochemicals. It is important to handle 2,6-DINITRO-4-IODOBENZOIC ACID with care, as it is toxic if ingested or inhaled and can cause irritation to the skin and eyes upon contact. It is also harmful to aquatic organisms and should be disposed of properly to prevent environmental damage.
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 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.
