36339-31-8

Basic information

• Product Name: 9,10-Anthracenedione, 2-(phenylamino)-
• CAS NO: 36339-31-8
• Molecular Formula: C20H13NO2
• Molecular Weight: 299.329
• Mol File: 36339-31-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 9,10-Anthracenedione, 2-(phenylamino)-(CAS DataBase Reference)
• NIST Chemistry Reference: 9,10-Anthracenedione, 2-(phenylamino)-(36339-31-8)
• EPA Substance Registry System: 9,10-Anthracenedione, 2-(phenylamino)-(36339-31-8)

Safety Data

• Hazardous Substances Data: 36339-31-8(Hazardous Substances Data)

Upstream product

• 82-27-9 2-amino-1-chloroanthraquinone 
• 108-86-1 bromobenzene 
• 84-48-0 2-sulfo-anthraquinone 
• 62-53-3 aniline 
• 591-50-4 iodobenzene 
• 117-79-3 2-aminoanthraquinone 
• 131-08-8 sodium anthraquinone-2-sulfonate 
• 131-09-9 2-chloroanthracene-9,10-dione 

Downstream Products

• 52869-16-6 2-(N-methyl-anilino)-anthraquinone 
• 321945-76-0 1,2-dianilino-anthraquinone 
• 109871-20-7 [2]anthryl-phenyl-amine 
• 72-48-0 1,2-dihydroxy-9,10-anthracenedione 
• 68637-85-4 1-Hydroxy-2-phenylaminoanthraquinone 

Relevant articles and documents

ARYLATION OF 2-AMINOANTHRAQUINONES BY HALOGENOBENZENES

2-Amino-, 1-chloro-2-amino-, and 2-amino-3-chloroanthraquinones react with halogenobenzenes in nitrobenzene in the presence of an acid-combining agent and copper catalyst to form initially 2-phenylaminoanthraquinones, which are then converted into 2-(diphenylamino)anthraquinones.In the reaction of 1-chloro-2-aminoanthraquinone with halogenobenzenes, in addition to mono- and diarylation of the amino group dehalogenation of the anthraquinone ring occurs both in the initial compound and in the arylation products, and N,N'-diphenylindanthrene is also formed.