1448670-20-9

Basic information

• Product Name: 5-methyl-11-phenylisoindolo[2,1-a]quinoline-7,10-dione
• CAS NO: 1448670-20-9
• Molecular Weight: 337.378
• Mol File: 1448670-20-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 5-methyl-11-phenylisoindolo[2,1-a]quinoline-7,10-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 5-methyl-11-phenylisoindolo[2,1-a]quinoline-7,10-dione(1448670-20-9)
• EPA Substance Registry System: 5-methyl-11-phenylisoindolo[2,1-a]quinoline-7,10-dione(1448670-20-9)

Safety Data

• Hazardous Substances Data: 1448670-20-9(Hazardous Substances Data)

Upstream product

• 402822-93-9 N-allyl-N-benzyl-2-(1-methylvinyl)aniline 
• 490035-95-5 N-benzyl-2-(prop-1-en-2-yl)benzen-amine 
• 110674-68-5 1-phenyl-N-(2-(prop-1-en-2-yl)phenyl)methanimine 
• 106-51-4 p-benzoquinone 
• 402822-97-3 1-benzyl-4-methyl-1,2-dihydro-quinoline 
• 52562-19-3 2-isopropenylaniline 
• 134-20-3 2-carbomethoxyaniline 
• 15833-00-8 o-aminophenyldimethylcarbinol 

Relevant articles and documents

One-pot ring-closing metathesis/1,3-dipolar cycloaddition through assisted tandem ruthenium catalysis: Synthesis of a dye with isoindolo[2,1-a]quinoline structure

The one-pot tandem reaction of N-alkyl-N-allyl-2-vinylaniline derivatives with benzo- or naphthoquinones and a ruthenium-alkylidene catalyst leads to isoindolo[2,1-a]quinolines in a variety of colors, which can be altered by exchanging the substituent on the core heterocycle (see scheme). This reaction offers a new synthetic method for π-conjugated small molecules from simple aniline derivatives. Copyright