≥96% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Normal Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
6,11-Dihydroxy-5,12-naphthacenedione is used in the synthesis of tetracene derivatives, Rhenium and Rhodium compounds, as well as, supramolecular coordination complexes.
| Canonical Smiles | C1=CC=C2C(=C1)C(=C3C(=C2O)C(=O)C4=CC=CC=C4C3=O)O |
|---|---|
| IUPAC Name | 6,11-dihydroxytetracene-5,12-dione |
| InChIKey | QECAURYYBPUIFF-UHFFFAOYSA-N |
| 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 |
| Isomeric SMILES | C1=CC=C2C(=C1)C(=C3C(=C2O)C(=O)C4=CC=CC=C4C3=O)O |
| WGK Germany | 3 |
| Molecular Weight | 290.27 |
| Reaxy-Rn | 1888609 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1888609&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Naphthacenes |
| Subclass | Tetracenequinones |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Tetracenequinones |
| Alternative Parents | Anthraquinones Naphthols and derivatives Hydroquinones Aryl ketones Vinylogous acids Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aromatic homopolycyclic compounds |
| Substituents | Tetracenequinone - 1,4-anthraquinone - 9,10-anthraquinone - 1-naphthol - Aryl ketone - Hydroquinone - Phenol - Vinylogous acid - Ketone - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aromatic homopolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as tetracenequinones. These are polyaromatic hydrocarbon derivatives containing a tetracyclic cycle made up of four linearly fused benzene rings, one of which bears two ketone groups at position 1 and 4. |
| External Descriptors | Not available |
| Melt Point(°C) | 350-351° C (lit.) |
|---|---|
| Molecular Weight | 290.300 g/mol |
| XLogP3 | 4.500 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 4 |
| Rotatable Bond Count | 0 |
| Exact Mass | 290.058 Da |
| Monoisotopic Mass | 290.058 Da |
| Topological Polar Surface Area | 74.600 Ų |
| Heavy Atom Count | 22 |
| Formal Charge | 0 |
| Complexity | 443.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
