86884-02-8

Basic information

• Product Name: (9R)-5-[[(9R)-8,9-Dihydro-3,4,7-trihydroxy-1,8,8,9-tetramethyl-6-oxo-6H-phenaleno[1,2-b]furan-5-yl]imino]-8,9-dihydro-3,7-dihydroxy-1,8,8,9-tetramethyl-4H-phenaleno[1,2-b]furan-4,6(5H)-dione
• Synonyms: (9R)-5-[[(9R)-8,9-Dihydro-3,4,7-trihydroxy-1,8,8,9-tetramethyl-6-oxo-6H-phenaleno[1,2-b]furan-5-yl]imino]-8,9-dihydro-3,7-dihydroxy-1,8,8,9-tetramethyl-4H-phenaleno[1,2-b]furan-4,6(5H)-dione;Scleroderris blue
• CAS NO: 86884-02-8
• Molecular Formula: C38H33NO10
• Molecular Weight: 663.66932
• Mol File: 86884-02-8.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 940.5±75.0 °C(Predicted)
• Appearance: /
• Density: 1.60±0.1 g/cm3(Predicted)
• PKA: 4.50±1.00(Predicted)
• CAS DataBase Reference: (9R)-5-[[(9R)-8,9-Dihydro-3,4,7-trihydroxy-1,8,8,9-tetramethyl-6-oxo-6H-phenaleno[1,2-b]furan-5-yl]imino]-8,9-dihydro-3,7-dihydroxy-1,8,8,9-tetramethyl-4H-phenaleno[1,2-b]furan-4,6(5H)-dione(CAS DataBase Reference)
• NIST Chemistry Reference: (9R)-5-[[(9R)-8,9-Dihydro-3,4,7-trihydroxy-1,8,8,9-tetramethyl-6-oxo-6H-phenaleno[1,2-b]furan-5-yl]imino]-8,9-dihydro-3,7-dihydroxy-1,8,8,9-tetramethyl-4H-phenaleno[1,2-b]furan-4,6(5H)-dione(86884-02-8)
• EPA Substance Registry System: (9R)-5-[[(9R)-8,9-Dihydro-3,4,7-trihydroxy-1,8,8,9-tetramethyl-6-oxo-6H-phenaleno[1,2-b]furan-5-yl]imino]-8,9-dihydro-3,7-dihydroxy-1,8,8,9-tetramethyl-4H-phenaleno[1,2-b]furan-4,6(5H)-dione(86884-02-8)

Safety Data

• Hazardous Substances Data: 86884-02-8(Hazardous Substances Data)

Upstream product

• 105481-61-6 entatrovenetinone 

Relevant articles and documents

Metabolites produced by the Scleroderris canker fungus, Gremmeniella abietina. Part 1

The metabolites produced in liquid culture by the Ascomycetous fungus Gremmeniella abietina (Lagerb.).Morelet, the causative agent of Scleroderris canker in pines, have been investigated.The major metabolite, which we have named sclerodin, is (-)-4,7-dihydroxy-2,3,3,9-tetramethyl-2,3-dihydronaphthofuran-5,6-dicarboxylic anhydride (1), the enantiomer of the so-called "naphthalic anhydride from atrovenetin".Several highly colored compounds, including the enantiomer of atrovenetinone (3), the blue compound 6, the red acenaphthenequinone derivative 8 (sclerodione), and the yellow 8-hydroxysclerodione (8) has been transformed into sclerodin (1).