15248-70-1

Usage

Uses

Used in Chemical Industry:
2-(naphthalen-2-yl)anthracene is used as a precursor in the synthesis of dyes and pigments for various applications, such as coloring textiles, plastics, and paints. Its unique structure and properties contribute to the color intensity and stability of these products.
Used in Pharmaceutical Industry:
Although 2-(naphthalen-2-yl)anthracene is known for its toxic effects, it has potential applications in the development of fluorescent markers for biological imaging and diagnostics. Its fluorescence properties can be utilized to track and visualize cellular processes or to detect specific biomolecules.
Used in Environmental Monitoring:
Due to its persistence and potential toxic effects, 2-(naphthalen-2-yl)anthracene can be used as an indicator of environmental pollution. Monitoring its presence in soil, water, and air samples can help assess the level of contamination and inform remediation efforts.
However, it is crucial to handle and dispose of 2-(naphthalen-2-yl)anthracene with caution to minimize its harmful impact on human health and the environment. Further research is needed to explore its potential applications while addressing the associated risks.

Upstream product

• 2949-26-0 2-ethynylnaphthalene 
• 86457-71-8 2-(naphthalen-2-yl)oxirane 
• 66-99-9 β-naphthaldehyde 
• 7321-27-9 2-bromoanthracene 
• 32316-92-0 naphthalene-2-boronic acid 
• 602297-32-5 2-hydroxyanthracene trifluoromethanesulfonate 
• 605-32-3 2-hydroxy-9,10-anthraquinone 

Downstream Products

• 1206628-35-4 9,10-dibromo-2-(naphthalen-2-yl)anthracene 

Relevant academic research and scientific papers

MeOTf/KI-catalyzed efficient synthesis of 2-arylnaphthalenesviacyclodimerization of styrene oxides

The MeOTf/KI-catalyzed synthesis of 2-arylnaphthalene derivatives from aryl ethylene oxides in alcohol under ambient conditions is described. The present protocol has a higher atom efficiency and wider substrate applicability with excellent yields. The reaction proceeded using the aryl ethylene oxides to give 2-arylnaphthalenes either in homo-coupling or in cross-coupling. The reaction could also be carried out at the gram scale in minutes.

Anthracene organic luminescence compound, method for preparing same and organic electroluminescence device

The invention provides an anthracene organic luminescence compound. The anthracene organic luminescence compound is provided with structures shown as a formula I. Compared with other electron transport layer materials, the anthracene organic luminescence

NOVEL ANTHRACENE DERIVATIVE, MATERIAL FOR ORGANIC ELECTROLUMINESCENT ELEMENT, MATERIAL SOLUTION FOR ORGANIC ELECTROLUMINESCENT ELEMENT, ORGANIC ELECTROLUMINESCENT ELEMENT AND ELECTRONIC APPARATUS

PROBLEM TO BE SOLVED: To provide a novel anthracene derivative, and a material for an organic electroluminescent element that uses the same and can form an organic thin film by an application method. SOLUTION: The present invention provides an anthracene derivative represented by the formula (1). SELECTED DRAWING: Figure 1 COPYRIGHT: (C)2018,JPOandINPIT

Naphthyl substituted anthracene combining charge transport with light emission

By simply introducing the naphthyl group into the 2-position of anthracene, we synthesized a new anthracene derivative, NaAnt, which showed good charge transporting properties up to 1.10 cm2 V-1 s-1 and a photoluminescence quantum yield (PLQY) of 40.30%. The results indicate its potential applications in multifunctional optoelectronics.

Highly selective biaryl formation by the cyclooligomerization of arylethynes catalyzed by rhodium and ruthenium porphyrins

Rhodium and ruthenium porphyrins catalyze the one-pot formation of biaryl derivatives from arylethynes with high selectivity, giving interesting derivatives not easy to obtain using other different methods; the porphyrin catalysts can be recovered and reu