23674-16-0

Basic information

• Product Name: 9-(4-chlorophenyl)anthracene
• CAS NO: 23674-16-0
• Molecular Formula: C₂₀H₁₃Cl
• Molecular Weight: 288.7702
• Mol File: 23674-16-0.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 429°C at 760 mmHg
• Flash Point: 198.3°C
• Density: 1.229g/cm³
• Vapor Pressure: 3.63E-07mmHg at 25°C
• Refractive Index: 1.706
• CAS DataBase Reference: 9-(4-chlorophenyl)anthracene(CAS DataBase Reference)
• NIST Chemistry Reference: 9-(4-chlorophenyl)anthracene(23674-16-0)
• EPA Substance Registry System: 9-(4-chlorophenyl)anthracene(23674-16-0)

Safety Data

• Hazardous Substances Data: 23674-16-0(Hazardous Substances Data)

Upstream product

• 18793-94-7 2-benzyl-4'-chloro-benzophenone 
• 10035-10-6 hydrogen bromide 
• 64-19-7 acetic acid 
• 106-39-8 bromochlorobenzene 
• 100622-34-2 anthracene-9-boronic acid 
• 120-12-7 anthracene 
• 2028-74-2 p-chlorobenzenediazonium chloride 
• 1564-64-3 9-Bromoanthracene 
• 1679-18-1 4-Chlorophenylboronic acid 
• 90-44-8 anthracen-9(10H)-one 
• 873-77-8 (4-chlorphenyl)magnesium bromide 

Downstream Products

• 158902-12-6 9-Bromo-10-(4-chlorophenyl)anthracene 
• 124562-63-6 C₃₆H₂₃ClO₂ 

Relevant articles and documents

When Anthracene and Quinone Avoid Cycloaddition: Acid-Catalyzed Redox Neutral Functionalization of Anthracene to Aryl Ethers

Benzoquinone and 9-phenylanthracene barely undergo anticipated cycloaddition under acid catalysis. Instead, 9-anthracenyl aryl ethers are obtained as unexpected products. Mechanistic studies indicate that the reaction likely undergoes an ionic mechanism between protonated anthracene species and nucleophilic oxygen of 1,4-benzoquinone or 1,4-hydroquinone. A variety of 9-anthracenyl aryl ethers are constructed with this method. Produced anthracenyl aryl ethers are potential scaffolds for new fluorescent molecules.

NOVEL AROMATIC COMPOUND AND ORGANIC ELECTROLUMINESCNET ELEMENT CONTAINING THE SAME

A novel aromatic compound having an anthracene skeleton structure and an asymmetric molecular structure; and an organic electroluminescence device which comprises a cathode, an anode and an organic thin film layer comprising at least one layer containing