32050-01-4

Basic information

• Product Name: Naphtho[2,3-c]furan-1,3-dione, 6-methyl-4-(4-methylphenyl)-
• CAS NO: 32050-01-4
• Molecular Formula: C20H14O3
• Molecular Weight: 302.329
• Mol File: 32050-01-4.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Naphtho[2,3-c]furan-1,3-dione, 6-methyl-4-(4-methylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Naphtho[2,3-c]furan-1,3-dione, 6-methyl-4-(4-methylphenyl)-(32050-01-4)
• EPA Substance Registry System: Naphtho[2,3-c]furan-1,3-dione, 6-methyl-4-(4-methylphenyl)-(32050-01-4)

Safety Data

• Hazardous Substances Data: 32050-01-4(Hazardous Substances Data)

Upstream product

• 2227-58-9 3-(4-methylphenyl)prop-2-ynoic acid 

Downstream Products

• 78298-53-0 3-benzylidene-6-methyl-4-(p-tolyl)-naphtho<2,3-c>furan-1(3H)-one 
• 116761-35-4 6-methyl-2-phenyl-4-(p-tolyl)benzindan-1,3-dione 
• 116761-43-4 7-Methyl-3-[1-phenyl-meth-(Z)-ylidene]-9-p-tolyl-3H-naphtho[2,3-c]furan-1-thione 
• 116761-39-8 3-[1-Bromo-1-phenyl-meth-(E)-ylidene]-7-methyl-9-p-tolyl-3H-naphtho[2,3-c]furan-1-one 
• 116761-47-8 7-Methyl-3-[1-phenyl-meth-(Z)-ylidene]-2-propyl-9-p-tolyl-2,3-dihydro-benzo[f]isoindol-1-one 
• 116761-51-4 7-Methyl-3-[1-(4-nitro-phenyl)-meth-(Z)-ylidene]-2-phenyl-9-p-tolyl-2,3-dihydro-benzo[f]isoindol-1-one 
• 203937-08-0 6-Methyl-4-(4-methylphenyl)-naphtho[2,3-c]furan-1(3H)-one 

Relevant articles and documents

One-pot syntheses of blue-luminescent 4-aryl-1H-benzo[f]isoindole-1, 3(2H)-diones by T3P activation of 3-arylpropiolic acids

In situ activation of 3-arylpropiolic acids with T3P (n-propylphosphonic acid anhydride) initiates a domino reaction furnishing 4-arylnaphtho[2, 3-c]furan-1, 3-diones in excellent yields. Upon employing these anhydrides as reactive intermediates blue-lumi

1-phenyl -2,3-naphthalene carboxylic acid anhydride, and its process for synthesis of derivatives of

The invention discloses a synthesis method of 1-phenyl-2,3-naphthalene dicarboxylic anhydride and derivatives thereof. The synthesis method is used for synthesizing the 1-phenyl-2,3-naphthalene dicarboxylic anhydride compounds under an alkali condition in