53793-65-0

Basic information

• Product Name: (4,6-diamino-1,3-phenylene)bis(phenylmethanone)
• Synonyms: (4,6-diamino-1,3-phenylene)bis(phenylmethanone)
• CAS NO: 53793-65-0
• Molecular Weight: 316.359
• Mol File: 53793-65-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (4,6-diamino-1,3-phenylene)bis(phenylmethanone)(CAS DataBase Reference)
• NIST Chemistry Reference: (4,6-diamino-1,3-phenylene)bis(phenylmethanone)(53793-65-0)
• EPA Substance Registry System: (4,6-diamino-1,3-phenylene)bis(phenylmethanone)(53793-65-0)

Safety Data

• Hazardous Substances Data: 53793-65-0(Hazardous Substances Data)

Upstream product

• 873993-02-3 1,5-dibenzoyl-2,4-dibromo-benzene 
• 91997-32-9 4,6-dibromobenzene-1,3-dicarboxylic acid dichloride 
• 52496-56-7 pseudo-4,6-dibenzoylisophthaloyl chloride 
• 57475-53-3 4,6-dibenzoylisophthalamide 
• 89-32-7 Pyromellitic dianhydride 
• 52497-38-8 (4,6-dibenzoyl)isophthalic acid 
• 71-43-2 benzene 
• 616-72-8 4,6-dinitro-m-xylene 
• 1872-40-8 4,6-dinitrobenzene-1,3-dioic acid 
• 57475-52-2 (4,6-dinitro-1,3-phenylene)bis(phenylmethanone) 
• 89-87-2 2,4-dimethylnitrobenzene 

Downstream Products

• 1301749-63-2 2,8-bis(biphenyl)-4,6-diphenyl-1,9-anthrazoline 
• 1301749-70-1 2,8-bis(3-(N-ethyl-carbazole))-4,6-diphenyl-1,9-anthrazoline 
• 1301749-60-9 2,8-bis(4-tert-butylphenyl)-4,6-diphenyl-1,9-anthrazoline 
• 1301749-68-7 2,8-bis(2-flourenyl)-4,6-diphenyl-1,9-anthrazoline 
• 1301749-64-3 2,8-bis(4-phenoxylphenyl)-4,6-diphenyl-1,9-anthrazoline 
• 1301749-62-1 2,8-bis(4-triphenylamino)-4,6-diphenyl-1,9-anthrazoline 
• 1301749-59-6 2,4,6,8-tetraphenyl-1,9-anthrazoline 
• 1301749-61-0 2,8-bis(4-methoxyphenyl)-4,6-diphenyl-1,9-anthrazoline 
• 1301749-67-6 2,8-bis(4-(9H-carbazol-9-yl)phenyl)-4,6-diphenyl-1,9-anthrazoline 
• 525-18-8 10,12-dihydroindeno<2,1-b>fluorene 

Relevant articles and documents

Synthesis and Electronic Properties of Novel 5,7-Diazapentacene Derivatives

A route to the synthesis of novel 5,7-diazapentacenes and some preliminary studies on their properties is reported. A single crystal X-ray diffraction study of the dihexyl derivative showed it had formed a dimer during the analysis. The materials possess lower lying frontier orbitals than pentacene and may have potential applications in organic electronic devices. This synthetic method may be applicable to the synthesis of other azaacenes.