31029-96-6

Basic information

• Product Name: 1-(4-AMINOPHENYL)-2-PHENYL-1,2-ETHANEDIONE
• Synonyms: 1-(4-AMINOPHENYL)-2-PHENYL-1,2-ETHANEDIONE
• CAS NO: 31029-96-6
• Molecular Formula: C₁₄H₁₁NO₂
• Molecular Weight: 225.24
• Mol File: 31029-96-6.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1-(4-AMINOPHENYL)-2-PHENYL-1,2-ETHANEDIONE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-AMINOPHENYL)-2-PHENYL-1,2-ETHANEDIONE(31029-96-6)
• EPA Substance Registry System: 1-(4-AMINOPHENYL)-2-PHENYL-1,2-ETHANEDIONE(31029-96-6)

Safety Data

• Hazardous Substances Data: 31029-96-6(Hazardous Substances Data)

Upstream product

• 1849-25-8 4-phenylethynylphenylamine 
• 66749-85-7 1-phenyl-2-(phenylimino)ethanone 
• 62-53-3 aniline 
• 98-86-2 acetophenone 
• 100-52-7 benzaldehyde 
• 122-85-0 para-acetamidobenzaldehyde 
• 101283-78-7 N-(α'-hydroxy-α-oxo-bibenzyl-4-yl)-acetamide 
• 31841-17-5 N-(4-(2-oxo-2-phenylacetyl)phenyl)acetamide 

Downstream Products

• 189680-69-1 6-(N,N-Dimethylamino)-4-[4-(1-phenyl-1,2-dioxoethyl-2-yl)anilino]-pyrido[3,4-d]pyrimidine hydrochloride 
• 81381-92-2 (R)-(-)-azabicyclo<2.2.2>oct-3-yl (RS)-α-hydroxy-α-<4-<2-(3-methylpiperidin-1-yl)-1,2-diazaethylen-1-yl>pheny>-α-phenylacetate 
• 81381-92-2 (S)-(+)-1-azabicyclo<2.2.2>oct-3-yl (RS)-α-hydroxy-α-<4-<2-(3-methylpiperidin-1-yl)-1,2-diazaethylen-1-yl>pheny>-α-phenylacetate 
• 81039-90-9 (R)-(-)-1-azabicyclo<2.2.2>oct-3-yl (RS)-α-hydroxy-α-(4-aminophenyl)-α-phenylacetate 
• 81039-90-9 (S)-(+)-azabicyclo<2.2.2>oct-3-yl (RS)-α-hydroxy-α-(4-aminophenyl)-α-phenylacetate 
• 81039-90-9 (RS)-1-azabicyclo<2.2.2>oct-3-yl (RS)-α-hydroxy-α-(4-aminophenyl)-α-phenylacetate 
• 88000-52-6 4-[(1-Aza-bicyclo[2.2.2]oct-3-yloxycarbonyl)-hydroxy-phenyl-methyl]-benzenediazonium; chloride 
• 81039-78-3 ethyl α-hydroxy-α-(4-aminophenyl)-α-phenylacetate 
• 81381-93-3 IQNB 
• 64946-35-6 4,4'-(3,3'-diphenyl-7,7'-oxy-di-quinoxalin-2-yl)-bis-aniline 
• 81381-90-0 α-hydroxy-α-(4-aminophenyl)-α-phenylacetic acid 

Relevant articles and documents

Metal-Free Iodine-Catalyzed Oxidation of Ynamides and Diaryl Acetylenes into 1,2-Diketo Compounds

Metal-free oxidation of ynamides is described, employing pyridine-N-oxides as oxidants under molecular iodine catalysis. In stark contrast to Br?nsted acid catalysis, iodophilic activation of ynamides diverts the reaction manifold into a dioxygenation pathway. This oxidation is very rapid at room temperature with only 2.5 mol % I2. Furthermore, this protocol could be extended to nonactivated alkynes, such as diarylacetylenes, to deliver various benzil derivatives.

Copper-catalyzed aerobic oxygenative cross dehydrogenative coupling of methyl ketones with: Para -C-H of primary anilines

A novel oxygenative cross dehydrogenative coupling of methyl ketones with para-C-H of primary anilines under a copper/oxygen catalytic system is described. This methodology features advantages including readily available starting materials, green oxidant, and broad functional group tolerance.