7,8-Benzoquinoline

From WikiMD's Wellness Encyclopedia


7,8-Benzoquinoline[edit | edit source]

7,8-Benzoquinoline is a heterocyclic aromatic organic compound that belongs to the class of quinoline derivatives. It is characterized by the fusion of a benzene ring with a quinoline structure, specifically at the 7 and 8 positions of the quinoline ring. This compound is of interest in various fields, including organic chemistry, medicinal chemistry, and materials science.

Structure and Properties[edit | edit source]

7,8-Benzoquinoline has the molecular formula C13H9N. It consists of a quinoline core, which is a bicyclic structure composed of a benzene ring fused to a pyridine ring, with an additional benzene ring fused at the 7 and 8 positions of the quinoline. This fusion results in a planar, aromatic structure that exhibits the typical properties of polycyclic aromatic hydrocarbons (PAHs).

The compound is a yellow crystalline solid at room temperature and is known for its stability and aromaticity. It has a melting point of approximately 70-72°C and is sparingly soluble in water but soluble in organic solvents such as ethanol, ether, and chloroform.

Synthesis[edit | edit source]

The synthesis of 7,8-Benzoquinoline can be achieved through several methods, including the Skraup synthesis, which involves the cyclization of aniline derivatives with glycerol and sulfuric acid in the presence of an oxidizing agent. Another method involves the Friedländer synthesis, which uses 2-aminobenzophenone derivatives and aldehydes under acidic conditions to form the quinoline ring system.

Applications[edit | edit source]

7,8-Benzoquinoline and its derivatives have been studied for their potential applications in various fields:

  • Medicinal Chemistry: As a quinoline derivative, 7,8-Benzoquinoline is of interest in the development of pharmaceuticals. Quinoline compounds are known for their antimalarial, antibacterial, and anticancer properties. Research is ongoing to explore the biological activity of 7,8-Benzoquinoline derivatives.
  • Materials Science: Due to its aromatic structure, 7,8-Benzoquinoline is studied for its potential use in organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaic cells.
  • Chemical Research: It serves as a building block in the synthesis of more complex organic molecules and is used in the study of aromaticity and heterocyclic chemistry.

Safety and Handling[edit | edit source]

As with many aromatic compounds, 7,8-Benzoquinoline should be handled with care. It is important to use appropriate personal protective equipment (PPE) such as gloves and goggles when handling the compound. It should be stored in a cool, dry place, away from sources of ignition.

Also see[edit | edit source]

Template:Quinoline derivatives

WikiMD
Navigation: Wellness - Encyclopedia - Health topics - Disease Index‏‎ - Drugs - World Directory - Gray's Anatomy - Keto diet - Recipes

Search WikiMD

Ad.Tired of being Overweight? Try W8MD's physician weight loss program.
Semaglutide (Ozempic / Wegovy and Tirzepatide (Mounjaro / Zepbound) available.
Advertise on WikiMD

WikiMD's Wellness Encyclopedia

Let Food Be Thy Medicine
Medicine Thy Food - Hippocrates

Medical Disclaimer: WikiMD is not a substitute for professional medical advice. The information on WikiMD is provided as an information resource only, may be incorrect, outdated or misleading, and is not to be used or relied on for any diagnostic or treatment purposes. Please consult your health care provider before making any healthcare decisions or for guidance about a specific medical condition. WikiMD expressly disclaims responsibility, and shall have no liability, for any damages, loss, injury, or liability whatsoever suffered as a result of your reliance on the information contained in this site. By visiting this site you agree to the foregoing terms and conditions, which may from time to time be changed or supplemented by WikiMD. If you do not agree to the foregoing terms and conditions, you should not enter or use this site. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates Wikipedia, licensed under CC BY SA or similar.

Contributors: Prab R. Tumpati, MD