61566-58-3 Usage
Uses
Used in Pharmaceutical Industry:
2,4-Diaminobenzoic acid dihydrochloride is used as a key intermediate in the synthesis of various pharmaceutical drugs. Its chemical structure allows for the development of new drug candidates with potential therapeutic applications.
Used in Dye Synthesis:
2,4-Diaminobenzoic acid dihydrochloride is used as a starting material in the production of dyes. Its chemical properties enable the creation of a wide range of dyes with different colors and properties.
Used in Analytical Chemistry:
2,4-Diaminobenzoic acid dihydrochloride is used as a component in the development of detecting and quantifying methods for pharmaceutical drugs. Its ability to react with specific compounds allows for accurate measurement and analysis of drug concentrations in various samples.
Used in Cancer Research:
2,4-Diaminobenzoic acid dihydrochloride is studied for its potential use in the treatment of certain medical conditions, such as cancer, due to its potential anticancer properties. Its chemical structure may contribute to the development of new cancer therapies and treatment options.
Check Digit Verification of cas no
The CAS Registry Mumber 61566-58-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,5,6 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 61566-58:
(7*6)+(6*1)+(5*5)+(4*6)+(3*6)+(2*5)+(1*8)=133
133 % 10 = 3
So 61566-58-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N2O2.2ClH/c8-4-1-2-5(7(10)11)6(9)3-4;;/h1-3H,8-9H2,(H,10,11);2*1H
61566-58-3Relevant academic research and scientific papers
Reduction of dinitrobenzenes by electron-carrying catalysts in the electrosynthesis of diaminobenzenes
Abakumov, M. V.,Leonova, M. Yu.,Mikhalchenko, L. V.,Novikov, V. T.,Zaplavin, A. P.
, p. 1927 - 1933 (2021/11/05)
The interaction of isomeric dinitrobenzenes (DNBs) with titanium(III), tin(II), and vanadium(II) chlorides, which are reducing agents used as electron carriers in the electrosynthesis of diaminobenzenes, has been studied. Rate constants of the reduction of isomeric DNBs and nitrophenylhydroxylamines by SnCl2 and TiCl3 in a 2 M water-alcohol solution (10 vol.% C2H5OH) of HCl were measured, and activation energies of the reduction of isomeric DNBs were determined. The rates of interaction of DNBs with the listed mediators increase in the series SnCl2 3 2. It is shown that the electrolysis of DNBs in the presence of an excess of these mediators makes it possible to obtain the corresponding diaminobenzenes with a yield of 60–90%.
