6,11-DIHYDROXY-5,12-NAPHTHACENEDIONE

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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

Click to get detail 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

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • BENZOHYDROQUINONE
  • Phthaloyl chloride
  • 3-phenylsulfanyl-3H-2-benzofuran-1-one
  • 1,4-naphthoquinone
  • 6,11-diphenoxy-5,12-naphthacenequinone
  • Dimethylamine hydrochloride
  • tetracene-5,6,11,12-tetrone
  • Phthalic anhydride
  • 6,11-diacetoxytetracene-5,12-dione
  • 6,11-dichloro-5,12-naphthacenequinone

DownStream

  • Tetracene
  • Perhydrotetracene
  • 5,12-Tetracenedione
  • 6,11-dimethoxytetracene-5,12-dione
  • tetracene-5,6,11,12-tetrone
  • 5,6,11,12-Tetrachlorotetracene
  • 5,12-Naphthacenedione,6-chloro-11-hydroxy-
  • Phthalic acid
  • benzoic acid

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

  • 1-Amino-6,11-dihydroxy-5,12-naphthacenedione
  • 7,8,9,10-tetrahydro-6,11-dihydroxy-5,12-naphthacenedione
  • 9-chloro-7,10-dihydro-6,11-dihydroxy-5,12-naphthacenedione
  • 8-acetyl-7,8,9,10-tetrahydro-6,11-dihydroxy-5,12-naphthacenedione
  • 9-(1-hydroxyethyl)-7,10-dihydro-6,11-dihydroxy-5,12-naphthacenedione
  • 9-(1-hydroxyethyl)-9,8(8H)-epoxy-7,10-dihydro-6,11-dihydroxy-5,12-naphthacenedione
  • N-Acetyl-3-(2-naphthalenyl)-D-alanyl-4-chloro-D-phenylalanyl-D-phenylalanyl-L-seryl-L-arginyl-3-(3-pyridinyl)-D-alanyl-L-leucyl-L-arginyl-L-prolyl-D-alaninamide
  • Chromate(1-), [3-[2-[4,5-dihydro-3-methyl-5-(oxo-kappaO)-1-phenyl-1H-pyrazol-4-yl]diazenyl-kappaN1]-4-(hydroxy-kappaO)benzenesulfonamidato(2-)][4-(hydroxy-kappaO)-3-[2-[2-(hydroxy-kappaO)-1-naphthalenyl]diazenyl-kappaN1]benzenesulfonamidato(2-)]-, sodium (1:1)
  • Chromate(1-), [N-[3-[2-[8-(acetylamino)-2-(hydroxy-kappaO)-1-naphthalenyl]diazenyl-kappaN1]-2-(hydroxy-kappaO)-5-nitrophenyl]acetamidato(2-)][4-(hydroxy-kappaO)-3-[2-[2-(hydroxy-kappaO)-1-naphthalenyl]diazenyl-kappaN1]-N-methylbenzenesulfonamidato(2-)]-, sodium (1:1)
  • Chromate(1-), bis[5-(1,1-dimethylethyl)-2-(hydroxy-kappaO)benzoato(2-)-kappaO]-, hydrogen (1:1)
  • Chromate(2-), [2,4-dihydro-4-[2-[2-(hydroxy-kappaO)-4-nitrophenyl]diazenyl-kappaN1]-5-methyl-2-phenyl-3H-pyrazol-3-onato(2-)-kappaO3][3-[2-[2-(hydroxy-kappaO)-4-hydroxyphenyl]diazenyl-kappaN1]-4-(hydroxy-kappaO)benzenesulfonato(3-)]-, hydrogen (1:2)
  • Chromate(2-), [2,4-dihydro-4-[2-[2-(hydroxy-kappaO)-5-nitrophenyl]diazenyl-kappaN1]-5-methyl-2-phenyl-3H-pyrazol-3-onato(2-)-kappaO3][4-(hydroxy-kappaO)-3-[2-[2-(hydroxy-kappaO)-1-naphthalenyl]diazenyl-kappaN1]benzenesulfonato(3-)]-, hydrogen (1:2)
  • Chromate(2-), [3-[2-[2-(amino-kappaN)-4-aminophenyl]diazenyl-kappaN1]-4-(hydroxy-kappaO)benzenesulfonato(3-)][1-[2-[2-(hydroxy-kappaO)-4-nitrophenyl]diazenyl-kappaN1]-2-naphthalenolato(2-)-kappaO]-, hydrogen (1:2)
  • Chromate(2-), [5-chloro-2-(hydroxy-kappaO)-3-[2-[1-(hydroxy-kappaO)-5-hydroxy-2-naphthalenyl]diazenyl-kappaN1]benzenesulfonato(3-)][1-[2-[2-(hydroxy-kappaO)-4-nitrophenyl]diazenyl-kappaN1]-2-naphthalenolato(2-)-kappaO]-, hydrogen (1:2)
  • Chromate(2-), [5-chloro-2-(hydroxy-kappaO)-3-[2-[2-(hydroxy-kappaO)-1-naphthalenyl]diazenyl-kappaN1]benzenesulfonato(3-)][1-[2-[2-(hydroxy-kappaO)-5-nitrophenyl]diazenyl-kappaN1]-2-naphthalenolato(2-)]-, hydrogen (1:2)
  • Chromate(3-), bis[3-hydroxy-7-nitro-4-[2-[2-oxo-1-[(phenylamino)carbonyl]propyl]diazenyl]-1-naphthalenesulfonato(3-)]-, hydrogen (1:3)
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