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quinoline    
n. 奎林

奎林


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  • Quinoline - 91-22-5, C9H7N, density, melting point, boiling point . . .
    Quinoline - cas 91-22-5, synthesis, structure, density, melting point, boiling point
  • Quinoline - Wikipedia
    Quinoline itself has few applications, but many of its derivatives are useful in diverse applications A prominent example is quinine, an alkaloid found in plants
  • Quinoline | Description, Drugs, Uses | Britannica
    Quinoline, any of a class of organic compounds of the aromatic heterocyclic series characterized by a double-ring structure composed of a benzene and a pyridine ring fused at two adjacent carbon atoms Several alkaloid quinoline compounds found in plants are important medicines
  • Quinoline | C9H7N | CID 7047 - PubChem
    Quinoline is the simplest member of the quinoline class of compounds, comprising a benzene ring ortho fused to C-2 and C-3 of a pyridine ring It is a mancude organic heterobicyclic parent, a member of quinolines, an azaarene and an ortho-fused heteroarene
  • Quinoline: Structure, Properties, and Applications
    Quinoline is a significant heterocyclic compound that has drawn considerable attention in various scientific areas It is important to understand its structure and properties, as they form the basis for its multiple applications
  • Quinoline: Structure, Properties Uses Explained - Vedantu
    Quinoline is a notable organic compound within the aromatic heterocyclic family, recognized for its fused double-ring structure Its unique chemistry makes it crucial in developing pharmaceuticals, dyes, and chemical synthesis
  • A comprehensive review on the biological interest of quinoline and its . . .
    Quinoline is a weak tertiary base It can form a salt with acids and displays reactions similar to those of pyridine and benzene It shows both electrophilic and nucleophilic substitution reactions It is non-toxic to humans on oral absorption and inhalation
  • Quinoline
    Quinoline is used mainly as an intermediate in the manufacture of other products Potential exposure to quinoline may occur from the inhalation of cigarette smoke Quinoline breaks down quickly in the atmosphere and water
  • The Chemistry and Applications of Quinoline: A Comprehensive Review
    Quinoline and its derivatives represent a vital class of heterocyclic compounds with wide-ranging pharmacological properties, including antimalarial, antimicrobial, anticancer, and anti-inflammatory activities
  • QUINOLINE | CAMEO Chemicals | NOAA
    QUINOLINE is hygroscopic It absorbs as much as 22% water It is sensitive to light and moisture It darkens on storage This chemical is a weak base A potentially explosive reaction may occur with hydrogen peroxide It reacts violently with dinitrogen tetraoxide It also reacts violently with perchromates





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