85292-69-9

Basic information

• Product Name: 9-(2-nitrophenyl)anthracene
• Synonyms: 9-(2-nitrophenyl)anthracene
• CAS NO: 85292-69-9
• Molecular Weight: 299.329
• Mol File: 85292-69-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 9-(2-nitrophenyl)anthracene(CAS DataBase Reference)
• NIST Chemistry Reference: 9-(2-nitrophenyl)anthracene(85292-69-9)
• EPA Substance Registry System: 9-(2-nitrophenyl)anthracene(85292-69-9)

Safety Data

• Hazardous Substances Data: 85292-69-9(Hazardous Substances Data)

Upstream product

• 120-12-7 anthracene 
• 119-66-4 2-nitrobenzenediazonium chloride 
• 100622-34-2 anthracene-9-boronic acid 
• 88-73-3 2-Chloronitrobenzene 
• 1564-64-3 9-Bromoanthracene 
• 5570-19-4 2-nitrophenylboronic acid 
• 577-19-5 2-nitrophenyl bromide 
• 98-95-3 nitrobenzene 
• 86-74-8 9H-carbazole 

Downstream Products

• 1252763-38-4 2-(anthracen-9-yl)aniline 
• 1060-61-3 9,10-bis-(2-nitro-phenyl)-anthracene 

Relevant articles and documents

Iptycenes with an acridinone motif developed through [4+2] cycloaddition of tethered naphthalene and iminoquinone: Via a radical reaction

A new class of iptycenes was developed by combining 2-(naphthalen-1-yl)anilines and p-benzoquinones through copper(ii)-mediated radical cyclisation. This unusual cyclisation reaction resulted in the robust and efficient syntheses of iptycenes with an acridinone motif. These iptycenes can be further transformed into planar acridinone heterocyclics through the Diels-Alder reaction.

NOVEL COMPOUNDS, ORGANIC LIGHT EMITTING DEVICE DISPLAY AND ORGANIC SOLAR BATTERY USING THE SAME

The present invention refers to a fullerene derivative is denoted by chemical formula 1 a, including organic light emitting diode and same relates to organic solar cells. In said formula 1, R 1 to R 6, Ar 1, A, X and n as defined in the application equal the specification.

Reaction of Carbazolylpotassium with 9-Bromoanthracene and Nitrobenzene

The formation of 9-(9-anthryl)carbazole (5) and 9-(2-nitrophenyl)anthracene (6) from 9-bromoanthracene (4), carbazole and nitrobenzene in the presence of potassium carbonate and catalytic amounts of copper is explained with the assumption of a trans-metallation equilibrium between carbazolylpotassium and nitrobenzene.