Name: Name:5,12-Naphthacenequinone
Brand: AABLOCKS
SKU: AA003M5U
Rating: 90 (10 reviews)

Technical Information

Catalog Number: AA003M5U

Chemical Name: 5,12-Naphthacenequinone

CAS Number: 1090-13-7

Molecular Formula: C18H10O2

Molecular Weight: 258.2708

MDL Number: MFCD00003701

SMILES: O=C1c2cc3ccccc3cc2C(=O)c2c1cccc2

NSC Number: 401183

Properties

BP: 472.5°C at 760 mmHg

Form: Solid

MP: 282-286 °C (dec.);(lit.);

Refractive Index: 1.5200 (estimate)

Storage: Keep in dry area;Room Temperature;

Complexity: 387

Covalently-Bonded Unit Count: 1

Defined Atom Stereocenter Count: 0

Defined Bond Stereocenter Count: 0

Formal Charge: 0

Heavy Atom Count: 20

Hydrogen Bond Acceptor Count: 2

Hydrogen Bond Donor Count: 0

Isotope Atom Count: 0

Rotatable Bond Count: 0

Undefined Atom Stereocenter Count: 0

Undefined Bond Stereocenter Count: 0

XLogP3: 4.6

Literature fold

Title: Comparative developmental toxicity of environmentally relevant oxygenated PAHs.

Journal: Toxicology and applied pharmacology20130901

Title: Selective accurate-mass-based analysis of 11 oxy-PAHs on atmospheric particulate matter by pressurized liquid extraction followed by high-performance liquid chromatography and magnetic sector mass spectrometry.

Journal: Analytical and bioanalytical chemistry20120201

Title: Phenol transformation photosensitised by quinoid compounds.

Journal: Physical chemistry chemical physics : PCCP20110621

Title: Effects of quinone derivatives, such as 1,4-naphthoquinone, on DNA polymerase inhibition and anti-inflammatory action.

Journal: Medicinal chemistry (Shariqah (United Arab Emirates))20110101

Title: Metabolic enzyme induction by HepG2 cells exposed to oxygenated and nonoxygenated polycyclic aromatic hydrocarbons.

Journal: Chemical research in toxicology20070201

Title: Synthesis and study of naphthacenedione (TQ) as a photosensitizer for one-electron oxidation of DNA.

Journal: Organic letters20041014

Title: Quinonic derivatives active against Toxoplasma gondii.

Journal: Parasitology research20021101

Title: Photochemical properties of the triplet pi,pi* state, anion and ketyl radicals of 5,12-naphthacenequinone in solution studied by laser flash photolysis: electron transfer and phenolic H-atom transfer.

Journal: Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology20021101

Title: Electronic structure of the lowest excited triplet state of 5,12-naphthacenequinone.

Journal: Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy20020401

1090-13-7 | 5,12-Naphthacenequinone