Chrysenequinone, with the CAS number 2051-10-7, is a polycyclic aromatic compound characterized by its fused ring structure, which includes a quinone functional group. This compound is derived from chrysene, a well-known polycyclic aromatic hydrocarbon (PAH), and exhibits properties typical of quinones, such as being a potent electrophile due to the presence of carbonyl groups. Chrysenequinone is generally insoluble in water but soluble in organic solvents, reflecting its hydrophobic nature. It is known for its potential biological activity, including mutagenic and carcinogenic properties, which are common among many PAHs and their derivatives. The compound can participate in redox reactions, making it relevant in various chemical and biological processes. Additionally, chrysenequinone can be used as an intermediate in organic synthesis and may have applications in materials science and medicinal chemistry. However, due to its toxicological profile, handling and usage require caution in laboratory and industrial settings.

chrysenequinone

2051-10-7: 5,6-Chrysenedione, 5,6-Chrysenequinone, 5,6-Chrysoquinone, Brn 0650510, Ccris 2025, Chrysene-5,6-Dione, Chrysene-5,6-quinone, Nsc 5192,  4-07-00-02646 (Beilstein Handbook Reference),  Chrysenequinone, Chrysenequinone

Applications 5,​6-​Chrysenedione is a useful reactant for organic reactions. It is a polycyclic aromatic hydrocarbon quinones, and studied as possible carcinogens.
References Boyle, K.M., et al.: J. Am. Chem. Soc., 140, 5612-24 (2018); Shultz, C.A., et al.: Chem. Res. Toxicol., 24, 2153-66 (2011);


CAS 2051-10-7: chrysenequinone

5,6-Chrysenedione

Ref: TR-C433210