4523-36-8

Usage

Uses

Used in Organic Synthesis:
N-phenyl-1-[(E)-phenyldiazenyl]naphthalen-2-amine is utilized as a key intermediate in organic synthesis for the creation of various complex organic molecules. Its unique structure allows for versatile chemical reactions, facilitating the synthesis of a range of compounds with potential applications in different fields.
Used in Materials Science:
In the field of materials science, N-phenyl-1-[(E)-phenyldiazenyl]naphthalen-2-amine is employed as a component in the development of new materials. Its specific chemical properties may contribute to the creation of materials with enhanced characteristics, such as improved stability, reactivity, or selectivity in certain applications.
Used in Pharmaceutical Research and Development:
N-phenyl-1-[(E)-phenyldiazenyl]naphthalen-2-amine holds potential in pharmaceutical research and development due to its distinctive chemical structure. It may serve as a lead compound for the design of new drugs or as a building block in the synthesis of bioactive molecules. However, further research is necessary to determine its efficacy, safety, and appropriate applications in medicine.

Upstream product

• 2684-02-8 benzenediazonium 
• 135-88-6 N-Phenyl-2-naphthylamine 
• 5488-73-3 [2]naphthyl-nitroso-phenyl-amine 
• 64-19-7 acetic acid 
• 62-53-3 aniline 
• 7732-18-5 water 
• 56862-95-4 2,3-diphenyl-naphtho[1,2-d][1,2,3]triazolium; chloride 

Downstream Products

• 38369-74-3 1-Amino-2-anilino-naphthalin 
• 56862-95-4 2,3-diphenyl-naphtho[1,2-d][1,2,3]triazolium; chloride 
• 62-53-3 aniline 

Relevant academic research and scientific papers

Stable and easily accessible functional dyes: Dihydrotetraazaanthracenes as versatile precursors for higher acenes

Abstract A series of new dihydrotetraazaanthracenes and one new dihydrotetraazatetracene as substances for applications in organoelectronic devices and as suitable building blocks for higher azaacenes was synthesised. The condensation of aromatic diamines with dichlorodicyanopyrazine led to these tricyclic/tetracyclic compounds. Syntheses of N-substituted phenylenediamines were developed to enable the introduction of multiple functional groups such as ester, amino, or nitro groups on the chromophoric system. Relationships between the structure and the spectroscopic properties could be derived from UV/Vis absorption and fluorescence spectroscopy, as well as by DFT and TD-DFT calculations of molecular and aggregate structures. The absorption spectra are dominated by π-π transitions of the single molecules, whereas aggregation needs to be taken into account to obtain reasonable agreement between theory and experiment in certain cases. Single-crystal X-ray analyses were carried out to examine the morphology and solid packing effects. Finally, a dihydrotetraazaanthracene was used as a building-block to create a mesoionic octaazapentacene. Dihydroazaacenes: A series of dihydrotetraazaanthracenes and one new dihydrotetraazatetracene as substances for applications in organoelectronic devices and as suitable building blocks for higher azaacenes was synthesised. Single-crystal X-ray analyses were carried out to examine the morphology and solid packing effects. Finally, a dihydrotetraazaanthracene was used as a building-block to create a mesoionic octaazapentacene.

TAUTOMERIC TRANSFORMATIONS AND COLOR OF MONOAZO DYES. II. DYES BASED ON PHENYL(NAPHTHYL)AMINES

In neutral solvents and glacial acetic acid monoazo dyes based on phenyl(1-naphthyl)amine are present mainly in the azo form.In aqueous acetic acid (30-90percent) they are present in the quinone-hydrazone tautomeric form.In neutral solvents and acetic aci