2,8-Dihydroxyhexahydrochrysene

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Chemical compound



2,8-Dihydroxyhexahydrochrysene[edit | edit source]

2,8-Dihydroxyhexahydrochrysene is a chemical compound that belongs to the class of organic compounds known as polycyclic aromatic hydrocarbons (PAHs). These compounds contain multiple aromatic rings and are known for their stability and potential biological activity.

Structure and Properties[edit | edit source]

The structure of 2,8-Dihydroxyhexahydrochrysene consists of a hexahydrochrysene backbone with hydroxyl groups attached at the 2 and 8 positions. This configuration imparts specific chemical properties to the molecule, including its solubility and reactivity.

The presence of hydroxyl groups makes this compound a type of phenol, which can participate in hydrogen bonding and affect the compound's polarity. The hexahydrochrysene core is a saturated form of chrysene, a well-known PAH, which influences its chemical behavior and potential interactions with biological systems.

Synthesis[edit | edit source]

The synthesis of 2,8-Dihydroxyhexahydrochrysene typically involves the hydrogenation of chrysene followed by selective hydroxylation. This process requires careful control of reaction conditions to ensure the correct placement of hydroxyl groups and to maintain the integrity of the hexahydrochrysene structure.

Applications[edit | edit source]

2,8-Dihydroxyhexahydrochrysene is primarily of interest in research settings, where it is studied for its potential biological activities. Compounds of this nature are often investigated for their interactions with biological membranes, enzymes, and receptors.

Biological Activity[edit | edit source]

The biological activity of 2,8-Dihydroxyhexahydrochrysene is an area of ongoing research. As a polycyclic aromatic compound with hydroxyl groups, it may exhibit activity in biological systems, potentially influencing cell signaling pathways or interacting with DNA.

Related pages[edit | edit source]

Gallery[edit | edit source]

2,8-Dihydroxyhexahydrochrysene[edit | edit source]

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