Interesting facts
              Interesting Facts about Quinolin-6-amine
Quinolin-6-amine is an intriguing compound that holds a significant place in the realm of organic chemistry and medicinal applications. Here are some interesting points about this unique chemical:
- Structural Significance: Quinolin-6-amine belongs to the class of aminoquinolines, which are derived from quinoline, a bicyclic compound known for its aromatic properties. The amine group at the 6-position adds to its reactivity and functional versatility.
- Biological Relevance: This compound has garnered interest in the field of pharmaceuticals due to its potential as a building block for various biologically active molecules. Its derivatives are explored for their anticancer, antimicrobial, and antiviral properties.
- Synthesis Approach: Chemists can synthesize quinolin-6-amine through diverse methods, including the reduction of corresponding nitro or nitrile derivatives. This flexibility is appealing for developing customized compounds for specific applications.
- Research Applications: Research studies have highlighted quinolin-6-amine and its derivatives in medicinal chemistry research, particularly in developing drugs targeting diseases such as malaria and other tropical diseases.
- Potential in Luminescent Materials: There is ongoing exploration of quinolin-6-amine in the development of luminescent materials, making it an exciting candidate for applications in organic light-emitting diodes (OLEDs) and organic photovoltaic cells.
In conclusion, quinolin-6-amine is more than just a simple amine; it is a compound with rich structural features and a wide array of applications in both basic and applied sciences. The ongoing research and developments surrounding this compound emphasize its importance in modern chemistry and potential future uses in various fields.
Synonyms
          6-AMINOQUINOLINE
          580-15-4
          6-Quinolinamine
          Quinoline, 6-amino-
          Quinolin-6-ylamine
          CCRIS 1681
          EINECS 209-453-0
          NSC 58388
          DTXSID80206725
          Quinoline, 6-amino-(8CI)
          DTXCID10129216
          rjsrsritmwviqt-uhfffaoysa-n
          Quinolin-6-amine
          MFCD00006803
          MLS000080747
          NSC-58388
          SMR000036663
          6-quinolylamine
          6-amino quinoline
          3kqp
          quinoline-6-amine
          6-Amino-quinoline
          quinolin-6-yl amine
          6-Aminoquinoline, 98%
          (Ziprasidone Impurity B)
          cid_11373
          BIDD:GT0636
          CHEMBL99408
          SCHEMBL160217
          XN7T264NL4
          SCHEMBL12280915
          BDBM32026
          HMS2451C16
          ALBB-014510
          NSC58388
          STK328120
          AKOS000131287
          AC-4708
          CS-W007404
          FA00884
          HY-W007404
          PS-4529
          SB67524
          SY021131
          DB-031615
          A1370
          NS00033833
          EN300-41836
          US8546389, 98
          AC-907/25014243
          Q27460051
          F2190-0533
          Z255114686
              
Solubility of Quinolin-6-amine
Quinolin-6-amine, with the chemical formula C9H8N2, exhibits interesting solubility characteristics. As an organic compound that belongs to the class of aminoquinolines, its solubility in various solvents can be significantly influenced by several factors:
In practical applications, the solubility profile of quinolin-6-amine is essential for its use in various chemical syntheses and pharmaceutical formulations. The following points help summarize its solubility behavior:
Understanding these solubility traits is crucial for effectively utilizing quinolin-6-amine in both laboratory and industrial settings.