Identification | Back Directory | [Name]
1 10-PHENANTHROLINE-5 6-DIONE 97 | [CAS]
27318-90-7 | [Synonyms]
phen-5,6-dione Stahl phd oxidant Phenanthroline-5,6- dipyridobenzoquinone Stahl phd oxidant phd 1,10-Phenanthrolin-5,6-dione 1,1-Phenanthroline-5,6-dione 1,10-Phenanthroline-5,6-dione 5H-cyclopenta dipyridin-5-one 1,10-Phenanthroline-5,6-quinone 1 10-PHENTHROLINE-5 6-DIONE 97 1,10-Phenanthroline-5,6-dione> 1,10-Phenanthroline-5,6-dione 97% 1 10-PHENANTHROLINE-5 6-DIONE 97 11,10-Phenanthroline-5,6-dione, 98% 5,6-dihydro-1,10-phenanthroline-5,6-dione 5,6-Dihydro-5,6-dioxo-1,10-phenanthroline 1,10-Phenanthroline-5,6-dione, 98%
Yellow to orange solid | [Molecular Formula]
C12H6N2O2 | [MDL Number]
MFCD00014473 | [MOL File]
27318-90-7.mol | [Molecular Weight]
210.19 |
Chemical Properties | Back Directory | [Melting point ]
260 °C (dec.)(lit.)
| [Boiling point ]
456.1±20.0 °C(Predicted) | [density ]
1.444±0.06 g/cm3(Predicted) | [storage temp. ]
Sealed in dry,Room Temperature | [form ]
powder to crystal | [pka]
0.26±0.20(Predicted) | [color ]
Light yellow to Amber to Dark green | [Water Solubility ]
Insoluble in water. | [λmax]
251nm(MeOH)(lit.) | [InChIKey]
KCALAFIVPCAXJI-UHFFFAOYSA-N |
Raw materials And Preparation Products | Back Directory | [Raw materials]
Ethanol-->Sodium hydroxide-->Sulfuric acid-->Nitric acid-->Chloroform-->Stannous chloride dihydrate-->Potassium bromide-->o-Phenanthroline-->1,10-Phenanthroline hydrate | [Preparation Products]
4,5,9,16-tetraaza-dibenzo[a,c]naphthacene-->2-(4-trifluoroMethylphenyl)iMidazole[4,5f][1,10]phenanthroline-->2-(2-trifluoroMethylphenyl)iMidazole[4,5f][1,10]phenanthroline-->2-(3-trifluoroMethylphenyl)iMidazole[4,5f][1,10]phenanthroline-->6-(4-METHOXYPHENYL)-2,2-DIMETHYL-[1,3]DIOXOLO[4,5-F][1,10]PHENANTHROLINE-->11,12-dimethyldipyrido[3,2-a:2',3'-c]phenazine-->tetrapyrido[3,2-a:2',3'-c:3'',2''-h:2''',3'''-j]phenazine |
Hazard Information | Back Directory | [Chemical Properties]
Yellow solid | [Uses]
A Bifunctional quinone oxidant | [General Description]
1,10-Phenanthroline-5,6-dione (phendio) forms Cu(II) and Ag(I) phendio complexes, which show potent anti-fungal and anti-cancer activity. The modification of glassy carbon (GC) electrodes with phendio complexes of transition metals leads to the catalytic oxidation of NADH at low overpotential. |
|
|