15248-70-1

Basic information

• Product Name: 2-(naphthalen-2-yl)anthracene
• Synonyms: 2-(naphthalen-2-yl)anthracene;2-(2-naphthalenyl)Anthracene
• CAS NO: 15248-70-1
• Molecular Formula: C24H16
• Molecular Weight: 304.38384
• EINECS: -0
• Mol File: 15248-70-1.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(naphthalen-2-yl)anthracene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(naphthalen-2-yl)anthracene(15248-70-1)
• EPA Substance Registry System: 2-(naphthalen-2-yl)anthracene(15248-70-1)

Safety Data

• Hazardous Substances Data: 15248-70-1(Hazardous Substances Data)

Usage

General Description

2-(naphthalen-2-yl)anthracene, also known as 2-(naphthalen-2-yl)anthracene, is a polycyclic aromatic hydrocarbon (PAH) compound with a molecular formula of C24H16. It is composed of two fused aromatic rings, a naphthalene and an anthracene, which are connected by a single bond. This chemical is commonly used in the manufacturing of dyes, pigments, and fluorescent materials. It is also a potential environmental pollutant due to its persistence in the environment and its toxic effects on living organisms. Studies have shown that 2-(naphthalen-2-yl)anthracene can cause DNA damage and is carcinogenic in nature. Therefore, it is important to handle and dispose of this chemical with caution to minimize its harmful impact on human health and the environment.

Upstream product

• 66-99-9 β-naphthaldehyde 
• 86457-71-8 2-(naphthalen-2-yl)oxirane 
• 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 
• 2949-26-0 2-ethynylnaphthalene 

Downstream Products

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

Relevant articles and documents

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.

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

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