Pronunciation: [kwˈɪnɐfənˌɪn] (IPA) 
Quinaphenin is a drug used to treat hypertension. Its pronunciation is /kwɪəˈnæfɪnɪn/, which means it is pronounced as "kwuh-nuh-fin-in". The first syllable "kwə" sounds like "kwa", while the second syllable "nə" sounds like "nuh". The final syllable "finin" sounds like "fin-in". Looking at the phonetic transcription, we can see that "quinaphenin" has a total of six syllables and is stress on the second syllable.
Quinaphenin is an organic compound that belongs to the class of compounds known as quinolinones. It is chemically characterized as a cyclic organic molecule consisting of a quinoline ring fused with a phenyl group. The compound has a molecular formula of C16H12N2O and a molecular weight of 248.28 g/mol.
Quinaphenin is primarily used in the field of pharmaceutical research due to its potential therapeutic properties. It possesses various biological activities, including anti-inflammatory, antioxidant, and antibacterial effects. These characteristics make it an interesting compound for the development of medicinal drugs.
In terms of its structural properties, quinaphenin features a flat, planar aromatic system. Its structure allows for diverse chemical reactions and interactions, which contribute to its potential biological functions. The compound's aromatic nature also renders it relatively stable under normal conditions.
Quinaphenin can be synthesized through various methods, including the Paal-Knorr synthesis and the Povarov reaction. These synthetic routes provide efficient access to the compound, facilitating its applications in both academic research and industrial processes.
Overall, quinaphenin is a quinolinone derivative that exhibits interesting biological activities, making it a promising candidate for the development of pharmaceuticals with potential anti-inflammatory, antioxidant, and antibacterial properties.
A compound of quinine and phenetidin, employed to meet the same indications as quinine.
A practical medical dictionary. By Stedman, Thomas Lathrop. Published 1920.
