6,11-DIHYDROXY-5,12-NAPHTHACENEDIONE
6,11-DIHYDROXY-5,12-NAPHTHACENEDIONE Basic information
- Product Name:
- 6,11-DIHYDROXY-5,12-NAPHTHACENEDIONE
- Synonyms:
-
- RARECHEM AR PA 0051
- 6,11-DIHYDROXY-5,12-NAPHTHACENEDIONE
- 6,11-DIHYDROXY-NAPHTHACENE-5,12-DIONE
- 6,11-DIHYDROXY-5,12-NAPHTHACENEDIONE, 98 %
- 6,11-DIHYDROXY-5,12-NAPHTHACENEDIONE 98%
- 5,12-Naphthacenedione, 6,11-dihydroxy-
- 6,11-dihydroxytetracene-5,12-dione
- 6,11-Dihydroxytertracene-5,12-dione
- CAS:
- 1785-52-0
- MF:
- C18H10O4
- MW:
- 290.27
- Product Categories:
-
- Miscellaneous
- C15 to C38
- Carbonyl Compounds
- Ketones
- Mol File:
- 1785-52-0.mol
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6,11-DIHYDROXY-5,12-NAPHTHACENEDIONE Chemical Properties
- Melting point:
- 350-351 °C (lit.)
- Boiling point:
- 552.9±45.0 °C(Predicted)
- Density
- 1.527±0.06 g/cm3(Predicted)
- pka
- 7.84±0.20(Predicted)
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MSDS
- Language:English Provider:SigmaAldrich
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6,11-DIHYDROXY-5,12-NAPHTHACENEDIONE Usage And Synthesis
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.
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