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Anthracene is a solid polycyclic aromatic hydrocarbon (PAH) of formula C 14 H 10, consisting of three fused benzene rings. It is a component of coal tar . Anthracene is used in the production of the red dye alizarin and other dyes, as a Scintillator to detect high energy particles, as production of pharmaceutical drugs.
The systematic IUPAC name is not always the preferred IUPAC name, for example, lactic acid is a common, and also the preferred, name for what systematic rules call 2-hydroxypropanoic acid. This list is ordered by the number of carbon atoms in a carboxylic acid.
9,10-Dihydroanthracene is an organic compound that is derived from the polycyclic aromatic hydrocarbon anthracene. Several isomers of dihydroanthracene are known, but the 9,10 derivative is most common. It is a colourless solid that is used as a carrier of H 2 as a hydrogen-donor. [2]
Benz[a]anthracene or benzo[a]anthracene is a polycyclic aromatic hydrocarbon with the chemical formula C 18 H 12. [2] It is produced during incomplete combustion of organic matter. Benz[ a ]anthracene is one of carcinogenic constituents of tobacco smoke .
Anthracene-9-carbaldehyde is the most common monoaldehyde derivative of anthracene. It is a yellow solid that is soluble in common organic solvents. It is prepared by Vilsmeier formylation of anthracene. [1] [2] The compound is also used as a building block for supramolecular assemblies. [3]
Tetracene, also called naphthacene, is a polycyclic aromatic hydrocarbon.It has the appearance of a pale orange powder. Tetracene is the four-ringed member of the series of acenes.
Anthraquinone, also called anthracenedione or dioxoanthracene, is an aromatic organic compound with formula C 14 H 8 O 2.Several isomers exist but these terms usually refer to 9,10-anthraquinone (IUPAC: 9,10-dioxoanthracene) wherein the keto groups are located on the central ring.
2 IUPAC name. 2 comments. 3 Diagram needed. 1 comment. 4 Toxicology reference. 2 comments. ... "Anthracene" is given as the IUPAC name at the PubChem link in the ...