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| SKU | Size | Availability |
Price | Qty |
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B434579-1g
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1g |
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
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$921.90
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| Synonyms | EINECS 202-138-9 | NAPHTHACENE [MI] | N0001 | naphthacene, benz[b]anthracene;tetracene, naphthacene, benz[b]anthracene | Benz(b)anthracene | FT-0695324 | AKOS024290196 | Chrysogen | MFCD00003702 | MLS000028646 | UNII-QYJ5Z6712R | Benz[b]anthracene | Benz[ |
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| Specifications & Purity | PrimorTrace™, sublimed grade, ≥99.99% metals basis |
| Grade | PrimorTrace™, sublimed grade |
| Product Description |
Benz[ b ]anthracene is an ethylnylated acene that is a conducting polymer, which can be used as a donor material. It has a high photoluminescence and quantum yield that makes it a promising candidate in the development of single crystal electronic material. Benz[ b ]anthracene is a fused polycyclic aromatic compound with an electron field-effect mobility of about 10 cm 2 /Vs Application p-Type organic conductor and OLED dopant. Sublimed grade for organic electronic device applications. Suitable for organic semiconductor lasers. Benz[ b ]anthracene can be used in a wide range of organic electronics based devices, which include organic light emitting diodes (OLEDs), solar cells, organic photovoltaics (OPVs), thin film transistors (TFTs), and other single crystal based organic semiconductors. |
Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Benzenoids |
| Class | Naphthacenes |
| Subclass | Not available |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Naphthacenes |
| Alternative Parents | Aromatic hydrocarbons Polycyclic hydrocarbons Unsaturated hydrocarbons |
| Molecular Framework | Aromatic homopolycyclic compounds |
| Substituents | Tetracene - Aromatic hydrocarbon - Polycyclic hydrocarbon - Unsaturated hydrocarbon - Hydrocarbon - Aromatic homopolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as naphthacenes. These are compounds containing a naphthacene moiety, which is a polyaromatic hydrocarbon made of four linearly fused benzene rings. |
| External Descriptors | tetracenes - acene |
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| Mechanism of Action | Action Type | target ID | Target Name | Target Type | Target Organism | Binding Site Name | References |
|---|
| IUPAC Name | tetracene |
|---|---|
| INCHI | InChI=1S/C18H12/c1-2-6-14-10-18-12-16-8-4-3-7-15(16)11-17(18)9-13(14)5-1/h1-12H |
| InChIKey | IFLREYGFSNHWGE-UHFFFAOYSA-N |
| Smiles | C1=CC=C2C=C3C=C4C=CC=CC4=CC3=CC2=C1 |
| Isomeric SMILES | C1=CC=C2C=C3C=C4C=CC=CC4=CC3=CC2=C1 |
| WGK Germany | 3 |
| Molecular Weight | 228.29 |
| Reaxy-Rn | 1909299 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1909299&ln= |
| Melt Point(°C) | 357℃ |
|---|---|
| Molecular Weight | 228.300 g/mol |
| XLogP3 | 5.900 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 0 |
| Rotatable Bond Count | 0 |
| Exact Mass | 228.094 Da |
| Monoisotopic Mass | 228.094 Da |
| Topological Polar Surface Area | 0.000 Ų |
| Heavy Atom Count | 18 |
| Formal Charge | 0 |
| Complexity | 236.000 |
| 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 |