73275-00-0

Upstream product

• 98-80-6 phenylboronic acid 
• 82-43-9 1,8-dichloroanthraquinone 
• 28557-00-8 phenylzinc chloride 
• 14381-66-9 1,8-dichloroanthracene 
• 33522-35-9 1,8-diphenyl anthracene 

Downstream Products

• 38305-28-1 1,8,10-Triphenylanthracene 
• 73275-02-2 10-Methyl-1,8-diphenyl-anthracene 
• 73275-15-7 1-(9-Methyl-4,5-diphenyl-anthracen-1-yl)-ethanone 
• 73275-16-8 1-(9-Methyl-4,5-diphenyl-anthracen-2-yl)-ethanone 

Relevant academic research and scientific papers

Condensed polycyclic aromatic hydrocarbon organic compound Composition, light-emitting device

The invention relates to a condensed-ring aromatic hydrocarbon organic compound, a composition and a light-emitting device. Wherein A, B, C, D, E, F and G are as defined in the claims. The condensed-ring aromatic hydrocarbon organic compound has a strong

ANTHRACENE DERIVATIVE AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME

The present invention relates to an anthracene derivative, which improves low driving voltage and/or lifetime characteristics in an organic light emitting device, and to an organic light emitting device including the same. The anthracene derivative is rep

ANTHRACENE BASED COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME

The present invention provides an anthracene-based compound and an organic light emitting device comprising same. Compounds of the present invention have a substituent group containing an aryl group at 1 and 8 positions of anthracene, and have a substituent group containing an aryl group or a heterocyclic group at 10 position, so that the luminous efficiency and lifetime of an organic light emitting device can be greatly improved when the compounds are applied to the organic light emitting device.COPYRIGHT KIPO 2018

Reactions of the 1,8-Diphenylanthracene System

An improved synthesis of 1,8-diphenylanthracene (1) is described along with various reactions of this hydrocarbon, including electrophilic substitution reactions, oxidations, and addition of n-BuLi.The molecular geometry of a derivative, 10-bromo-1,8-diphenylanthracene (20), was determined by X-ray crystallography.Of the various routes explored for forming 9-substituted 1,8-diphenylanthracenes, only the addition of certain organometallic reagents to the 9-anthrone 10 was satisfactory.