95192-57-7 Usage
Uses
Used in Pharmaceutical Industry:
4-CHLORO-2,6-DINITROBENZOIC ACID is used as a reagent for the synthesis of pharmaceuticals. Its unique structure allows it to be a key component in the creation of new and effective medications, contributing to advancements in healthcare.
Used in Agrochemical Industry:
4-CHLORO-2,6-DINITROBENZOIC ACID also serves as a reagent in the synthesis of agrochemicals. Its application in this field helps in the development of products that protect crops and enhance agricultural productivity.
Used in Dye and Pigment Production:
4-CHLORO-2,6-DINITROBENZOIC ACID is utilized as an intermediate in the production of dyes and pigments. Its presence in these compounds contributes to the colorfastness and stability of the final products, which are used in various industries such as textiles, plastics, and printing.
Safety Note:
Due to its toxic nature, 4-CHLORO-2,6-DINITROBENZOIC ACID should be handled with care to minimize potential health hazards. Proper safety measures and precautions are essential when working with this chemical compound.
Check Digit Verification of cas no
The CAS Registry Mumber 95192-57-7 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 95192-57:
(7*9)+(6*5)+(5*1)+(4*9)+(3*2)+(2*5)+(1*7)=157
157 % 10 = 7
So 95192-57-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H3ClN2O6/c8-3-1-4(9(13)14)6(7(11)12)5(2-3)10(15)16/h1-2H,(H,11,12)
95192-57-7Relevant 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.
