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1785-52-0

1785-52-0 Structure

1785-52-0 Structure
IdentificationBack Directory
[Name]

6,11-DIHYDROXY-5,12-NAPHTHACENEDIONE
[CAS]

1785-52-0
[Synonyms]

RARECHEM AR PA 0051
6,11-dihydroxytetracene-5,12-dione
6,11-Dihydroxytertracene-5,12-dione
6,11-DIHYDROXY-5,12-NAPHTHACENEDIONE
6,11-DIHYDROXY-NAPHTHACENE-5,12-DIONE
5,12-Naphthacenedione, 6,11-dihydroxy-
6,11-DIHYDROXY-5,12-NAPHTHACENEDIONE 98%
6,11-DIHYDROXY-5,12-NAPHTHACENEDIONE, 98 %
[Molecular Formula]

C18H10O4
[MDL Number]

MFCD00192048
[MOL File]

1785-52-0.mol
[Molecular Weight]

290.27
Chemical PropertiesBack Directory
[Melting point ]

350-351 °C (lit.)
[Boiling point ]

552.9±45.0 °C(Predicted)
[density ]

1.527±0.06 g/cm3(Predicted)
[form ]

solid
[pka]

7.84±0.20(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P305+P351+P338
[Hazard Codes ]

Xi
[Risk Statements ]

36/37/38
[Safety Statements ]

26-36
[WGK Germany ]

3
Hazard InformationBack Directory
[Uses]

6,11-Dihydroxy-5,12-naphthacenedione was used in the synthesis of a tetracene derivative, 5,6,11,12-tetrachlorotetracene. It was also used for the synthesis of (3Z,3′Z)-3,3′-(ethane-1,2-diylidene)bis[isobenzofuran-1(3H)-one]. It may be used for the following studies:
  • Synthesis of self-assembled, chair-shaped dirhenium(I) macrocyclic compounds.
  • Synthesis of half-sandwich Ir, Rh-based organometallic molecular boxes.
  • As ligand for the synthesis of supramolecular coordination complexes (SCCs).
[General Description]

Crystallographic analysis of 6,11-dihydroxy-5,12-naphthacenedione has been reported. Study indicates the presence of (3Z,3′Z)-3,3′-(ethane-1,2-diylidene)bis[isobenzofuran-1(3H)-one] as impurity.
Spectrum DetailBack Directory
[Spectrum Detail]

6,11-DIHYDROXY-5,12-NAPHTHACENEDIONE(1785-52-0)IR
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