33522-27-9

Upstream product

• 33522-35-9 1,8-diphenyl anthracene 
• 73274-96-1 C₂₆H₁₈O₂ 
• 30877-00-0 1,8-diiodo-anthraquinone 
• 591-51-5 phenyllithium 
• 28557-00-8 phenylzinc chloride 
• 16939-57-4 (E)-buta-1,3-dienylbenzene 
• 106-51-4 p-benzoquinone 
• 82-43-9 1,8-dichloroanthraquinone 
• 98-80-6 phenylboronic acid 
• 33522-29-1 5-phenyl-1,4-naphthoquinone 
• 14381-66-9 1,8-dichloroanthracene 
• 33522-32-6 1,8-Diphenyl-1,4-dihydro-anthraquinone 
• 33522-40-6 1,8-bis-(toluene-4-sulfonylamino)-anthraquinone 
• 129-42-0 1,8-diamino-anthraquinone 

Downstream Products

• 73275-03-3 10-Ethynyl-10-hydroxy-1,8-diphenyl-10H-anthracen-9-one 
• 38305-27-0 10-Hydroxy-1,8,10-triphenyl-10H-anthracen-9-one 
• 33522-39-3 1,8,9-Triphenylanthracen 
• 38305-28-1 1,8,10-Triphenylanthracene 
• 73275-05-5 9-Ethyl-1,8-diphenyl-anthracene 
• 73275-04-4 10-Ethyl-1,8-diphenyl-anthracene 
• 73275-06-6 1,8-Diphenyl-9-vinyl-anthracene 
• 33522-35-9 1,8-diphenyl anthracene 
• 33522-37-1 1,8-Diphenyl-<9>anthron 

Relevant academic research and scientific papers

COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME

The present invention relates to a compound represented by chemical formula 1 and to an organic light emitting device comprising the same. The compound is capable of improving efficiency, having low driving voltage, and/or improving service life properties in the organic light emitting device.

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.