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6,11-DIHYDROXY-5,12-NAPHTHACENEDIONE

Names

[ CAS No. ]:
1785-52-0

[ Name ]:
6,11-DIHYDROXY-5,12-NAPHTHACENEDIONE

[Synonym ]:
5,12-dihydroxy-6,13-tetracenequinone
6,11-Dihydroxy-5,12-naphthacenedione
6,11-dihydroxynaphthacene-5,12-dione
6,11-dihydroxy-5,12-naphthacenequinone
6,11-Dihydroxy-5,11-naphthacenequinone
MFCD00192048

Chemical & Physical Properties

[ Density]:
1.527g/cm3

[ Boiling Point ]:
552.9ºC at 760mmHg

[ Melting Point ]:
350-351ºC(lit.)

[ Molecular Formula ]:
C18H10O4

[ Molecular Weight ]:
290.27000

[ Flash Point ]:
302.2ºC

[ Exact Mass ]:
290.05800

[ PSA ]:
74.60000

[ LogP ]:
3.02640

[ Vapour Pressure ]:
7.82E-13mmHg at 25°C

[ Index of Refraction ]:
1.787

MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
36/37/38

[ Safety Phrases ]:
26-36

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2914690090

Synthetic Route

Precursor & DownStream

Customs

[ HS Code ]: 2914690090

[ Summary ]:
2914690090 other quinones。Supervision conditions:None。VAT:17.0%。Tax rebate rate:9.0%。MFN tariff:5.5%。General tariff:30.0%

Articles

Quinonoid-bridged chair-shaped dirhenium(I) metallacycles: synthesis, characterization, and spectroelectrochemical studies.

Inorg. Chem. 49(22) , 10264-72, (2010)

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-naphthacene...

Self-assembled half-sandwich Ir, Rh-based organometallic molecular boxes for reversible trapping of halocarbon molecules.

Dalton Trans. 39(16) , 3976-84, (2010)

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 = ...

5, 6, 11, 12-Tetrachlorotetracene, a tetracene derivative with p-stacking structure: The synthesis, crystal structure and transistor properties. Chi X, et al.

Org. Electron. 9(2) , 234-40, (2008)


More Articles


Related Compounds

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