409715
6,11-Dihydroxy-5,12-naphthacenedione
96%
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About This Item
Formula empirica (notazione di Hill):
C18H10O4
Numero CAS:
Peso molecolare:
290.27
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
![Benzo[h]quinoline 97%](/deepweb/assets/sigmaaldrich/product/structures/344/715/928932d2-4ca4-4402-b56c-85a80100ce17/640/928932d2-4ca4-4402-b56c-85a80100ce17.png)
Saggio
96%
Stato
solid
Punto di fusione
350-351 °C (lit.)
Gruppo funzionale
ketone
Stringa SMILE
Oc1c2C(=O)c3ccccc3C(=O)c2c(O)c4ccccc14
InChI
1S/C18H10O4/c19-15-9-5-1-2-6-10(9)16(20)14-13(15)17(21)11-7-3-4-8-12(11)18(14)22/h1-8,19-20H
QECAURYYBPUIFF-UHFFFAOYSA-N
Categorie correlate
Descrizione generale
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.
Applicazioni
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).
Avvertenze
Warning
Indicazioni di pericolo
Consigli di prudenza
Classi di pericolo
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
dust mask type N95 (US), Eyeshields, Gloves
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I clienti hanno visto anche
Dibyendu Bhattacharya et al.
Inorganic chemistry, 49(22), 10264-10272 (2010-10-16)
Self-assembled, chair-shaped dirhenium(I) macrocyclic compounds featuring the two different bis-chelating quinone dianions (1, L = dhnq(2-); 2, L = dhaq(2-); H(2)dhnq = 6,11-dihydroxy-5,12-naphthacenedione; H(2)dhaq = 1,4-dihydroxy-9,10-anthraquinone) that interface with two fac-Re(CO)(3) cores and a ditopic semirigid N-donor 1,4-bis(5,6-dimethylbenzimidazol-1-ylmethyl)naphthalene (L' =
Synthesis of rhenium-based M 2 LL'-type supramolecular coordination complexes from flexible ligands.
Shankar B, et al.
Journal of Organometallic Chemistry, 743, 109-113 (2013)
Ying-Feng Han et al.
Dalton transactions (Cambridge, England : 2003), 39(16), 3976-3984 (2010-04-08)
Reactions of [Cp*MCl(mu-Cl)](2) (M = Ir or Rh) with 6,11-dihydroxy-5,12-naphthacenedione (H(2)DHNA) in the presence of base, gave the corresponding binuclear complexes [Cp*(2)M(2)(mu-DHNA)Cl(2)] (M = Ir (1a); M = Rh (1b)), respectively. Treatment of 1a or 1b with bidentate ligands (L)
5, 6, 11, 12-Tetrachlorotetracene, a tetracene derivative with p-stacking structure: The synthesis, crystal structure and transistor properties.
Chi X, et al.
Organic Electronics, 9(2), 234-240 (2008)
(3Z, 3'Z)-3, 3'-(Ethane-1, 2-diylidene) bis [isobenzofuran-1 (3H)-one].
Ono K, et al.
Acta Crystallographica Section E, Structure Reports Online, 65(9), 2118-2118 (2009)
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