92-65-9

Usage

Uses

Used in Pharmaceutical Industry:
2-(4-amino-N-ethylanilino)ethanol is used as an intermediate in the synthesis of pharmaceuticals for its potential applications in the production of anti-inflammatory drugs and antibiotics. Its unique structure allows for the development of new therapeutic agents that can address various health conditions.
Used in Dye Industry:
In the dye industry, 2-(4-amino-N-ethylanilino)ethanol is used as an intermediate in the synthesis of various dyes. Its chemical properties contribute to the development of dyes with specific color characteristics and improved performance.
Used in Organic Compounds Synthesis:
2-(4-amino-N-ethylanilino)ethanol is utilized as a key intermediate in the synthesis of other organic compounds. Its presence in these compounds can enhance their properties, such as solubility, stability, or reactivity, making them suitable for a wide range of applications across different industries.

InChI:InChI=1/C10H16N2O/c1-2-12(7-8-13)10-5-3-9(11)4-6-10/h3-6,13H,2,7-8,11H2,1H3

Upstream product

• 92-50-2 2-( N-ethylanilino)ethanol 

Relevant academic research and scientific papers

Hypersensitive azobenzenes: Facile synthesis of clickable and cleavable azo linkers with tunable and high reducibility

The aim of this work is to show that by increasing the number of donor substituents in a donor/acceptor system, the sensitivity of the azobenzene linkage towards a reductive cleavage reaction can be enhanced to unprecedented high levels. For instance, in a triple-donor system, less than a second constitutes the half-life of the azo (NN) bond. Synthetic access to such redox active scaffolds is highly practical and requires only 1-2 synthetic steps. The fundamental molecular design is also adaptable. This is demonstrated through scaffold functionalization by azide, tetraethylene glycol, and biotin groups. The availability of the azide group is shown in a copper-free 'click' reaction suitable in context with protein conjugation and proteomics application. Finally, the clean nature of the scission process is demonstrated with the help of liquid chromatography coupled with mass analysis. This work, therefore, describes development of cleavable azobenzene linkers that can be accessed with synthetic ease, can be multiply functionalized, and show a clean and rapid response to mild reducing conditions.

1,3-Dihydroxybenzene derivatives and colorants containing said compounds

1,3-Dihydroxybenzene derivatives of general formula (I) or (Ia) or physiologically tolerated, water-soluble thereof wherein R′1 denotes substituted pyridyl group, a pyrimidyl group, a group of formula (IIa) or (IIIa) and the dyeing agents for keratin fibers containing these compounds.

Methine compounds

Methine compounds are described, which can be represented by general formula [Ic]: STR1

Oxidative hair dye compositions

Oxidative hair dye composition containing as "para component" compounds of the formula: SPC1 Or their acid addition salts, in which: R1 is alkyl or hydroxyalkyl; R2 is hydrogen or hydroxyalkyl; R3 is hydrogen, alkyl, alkoxy or halogen; and R4 occupies any one of the remaining positions on the benzene radical and is hydrogen, alkyl, alkoxy or halogen; providing that R2 is hydrogen when R3 is alkyl, alkoxy or halogen and providing that at least two of R1, R2, R3 or R4 are other than hydrogen.