33522-37-1

Upstream product

• 33522-27-9 1,8-Diphenyl-9,10-anthraquinon 
• 106-51-4 p-benzoquinone 
• 591-51-5 phenyllithium 
• 33522-40-6 1,8-bis-(toluene-4-sulfonylamino)-anthraquinone 
• 129-42-0 1,8-diamino-anthraquinone 
• 33522-32-6 1,8-Diphenyl-1,4-dihydro-anthraquinone 
• 33522-30-4 5-Phenyl-naphthalene-1,4-diol 
• 82-43-9 1,8-dichloroanthraquinone 
• 33522-29-1 5-phenyl-1,4-naphthoquinone 
• 16939-57-4 (E)-buta-1,3-dienylbenzene 
• 28557-00-8 phenylzinc chloride 
• 33522-35-9 1,8-diphenyl anthracene 
• 30877-00-0 1,8-diiodo-anthraquinone 
• 14381-66-9 1,8-dichloroanthracene 

Downstream Products

• 73275-05-5 9-Ethyl-1,8-diphenyl-anthracene 
• 73275-06-6 1,8-Diphenyl-9-vinyl-anthracene 
• 33522-39-3 1,8,9-Triphenylanthracen 
• 38305-37-2 9-Methoxy-1,8-diphenyl-anthracene 

Relevant academic research and scientific papers

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.