62024-69-5 Usage
Description
1,2-Ethanediamine, N-(2,4-dinitrophenyl)-, monohydrochloride is a chemical compound derived from ethylenediamine, featuring a 2,4-dinitrophenyl group and a monohydrochloride moiety. 1,2-Ethanediamine, N-(2,4-dinitrophenyl)-, monohydrochloride is known for its increased water solubility due to the presence of the monohydrochloride group, which makes it suitable for use in aqueous solutions. It is also recognized for its chelating properties and its ability to form complexes with metal ions, which is beneficial in various industrial applications and analytical chemistry.
Uses
Used in Pharmaceutical Synthesis:
1,2-Ethanediamine, N-(2,4-dinitrophenyl)-, monohydrochloride is used as an intermediate in the synthesis of pharmaceuticals for its ability to form complexes with metal ions, which can enhance the efficacy and stability of certain drugs.
Used in Dye Production:
In the dye industry, this compound is used as a precursor in the production of various dyes, where its complex-forming ability contributes to the development of dyes with specific properties.
Used in Pesticide Formulation:
1,2-Ethanediamine, N-(2,4-dinitrophenyl)-, monohydrochloride is utilized in the formulation of pesticides, where its chelating properties can improve the performance and stability of the active ingredients.
Used in Analytical Chemistry:
1,2-Ethanediamine, N-(2,4-dinitrophenyl)-, monohydrochloride is used as a reagent in analytical chemistry for metal ion detection and separation, taking advantage of its complex-forming capabilities with metal ions.
Used in Medical Research:
1,2-Ethanediamine, N-(2,4-dinitrophenyl)-, monohydrochloride has been investigated for its potential use in the treatment of various medical conditions, including cancer, due to its chemical properties and interactions with biological systems.
It is important to handle 1,2-Ethanediamine, N-(2,4-dinitrophenyl)-, monohydrochloride with care, as it is toxic and can cause irritation to the skin, eyes, and respiratory system. Proper safety measures should be taken during its use in any application.
Check Digit Verification of cas no
The CAS Registry Mumber 62024-69-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,0,2 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 62024-69:
(7*6)+(6*2)+(5*0)+(4*2)+(3*4)+(2*6)+(1*9)=95
95 % 10 = 5
So 62024-69-5 is a valid CAS Registry Number.
62024-69-5Relevant articles and documents
In silico design, synthesis, and assays of specific substrates for proteinase 3: Influence of fluorogenic and charged groups
Narawane, Shailesh,Budnjo, Adnan,Grauffel, Cédric,Haug, Bengt Erik,Reuter, Nathalie
supporting information, p. 1111 - 1115 (2014/03/21)
Neutrophil serine proteases are specific regulators of the immune response, and proteinase 3 is a major target antigen in antineutrophil cytoplasmic antibody-associated vasculitis. FRET peptides containing 2-aminobenzoic acid (Abz) and N-(2,4-dinitrophenyl)ethylenediamine (EDDnp) as fluorophore and quencher groups, respectively, have been widely used to probe proteases specificity. Using in silico design followed by enzymatic assays, we show that Abz and EDDnp significantly contribute to substrate hydrolysis by PR3. We also propose a new substrate specific for PR3.
Synthesis of (alkylamino)nitroarenes by oxidative alkylamination of nitroarenes
Gulevskaya, Anna V.,Verbeeck, Stefan,Burov, Oleg N.,Meyers, Caroline,Korbukova, Inna N.,Herrebout, Wouter,Maes, Bert U. W.
experimental part, p. 564 - 574 (2009/09/06)
The viability of the oxidative alkylamination process for the derivatization of electron-deficient carboaromatics has been investigated. 1,3-Dinitrobenzene, 1-nitronaphthalene, and 1,5- and 1,8-dinitronaphthalenes have shown to react with a wide range of alkylamines in the presence of an oxidant (KMnO4, AgMnO4, AgPy2MnO4) to give access to the corre sponding N-alkyl-nitroarenamines in moderate to good yields. Nitroarenes are more reactive than azines towards alkylamines.
