62024-69-5

Usage

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, 1,2-Ethanediamine, N-(2,4-dinitrophenyl)-, monohydrochloride 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.

Upstream product

• 99-65-0 meta-dinitrobenzene 
• 107-15-3 ethylenediamine 
• 333-18-6 1,2-diaminoethane dihydrochloride 
• 97-00-7 1-chloro-2,4-dinitro-benzene 

Downstream Products

• 923001-75-6 C₁₉H₂₇N₇O₉ 
• 873223-13-3 C₁₇H₂₄N₆O₈ 
• 154036-02-9 C₃₄H₄₀N₆O₉ 
• 28767-75-1 N¹-(2,4-dinitrophenyl)ethane-1,2-diamine 
• 154036-08-5 tert-butyl (S)-4-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-5-((2-((2,4-dinitrophenyl)amino)ethyl)amino)-5-oxopentanoate 

Relevant academic research and scientific papers

In silico design, synthesis, and assays of specific substrates for proteinase 3: Influence of fluorogenic and charged groups

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.

Nucleotides. Part LXXVIII: Double labeling of nucleosides and nucleotides

Several N(-hydroxyalkyl)-2,4-dinitroanilines were transformed into their phosphoramidites (see 5 and 6 in Scheme 1) in view of their use as fluorescence quenchers, and modified 2-aminobenzamides (see 9, 10, 18, and 19 in Scheme 1) were applied in model re

Synthesis of (alkylamino)nitroarenes by oxidative alkylamination of nitroarenes

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.