Interesting facts
              Interesting Facts About 6-Nitroquinoline
6-Nitroquinoline is a fascinating compound belonging to the class of heterocyclic organic compounds. Here are some intriguing aspects of this compound:
- Pharmaceutical Applications: This compound is commonly investigated for its potential role in medicinal chemistry, especially in the development of antimalarial and antimicrobial agents. Researchers are curious about its ability to inhibit certain enzymes in target pathogens.
- Fluorescent Properties: 6-Nitroquinoline exhibits unique fluorescent properties, making it a candidate for applications in fluorescence spectroscopy and microscopy. Its emission spectra can provide valuable information about the local environment of the molecule during experiments.
- Stability and Reactivity: The presence of the nitro group makes this compound more reactive than its non-nitro derivatives. This increased reactivity can lead to diverse synthetic pathways and products, intriguing many synthetic chemists.
- Biological Studies: Studies suggest that 6-nitroquinoline and its derivatives could function as inhibitors in various biological processes, providing insight into the mechanics of enzyme-reaction pathways.
- Research Significance: The compound serves as a key intermediate in organic synthesis, allowing chemists to explore a range of derivatives and their respective properties. Its versatility in synthesis makes it a valuable compound in research laboratories.
Overall, 6-nitroquinoline continues to captivate chemists due to its array of applications, reactivity, and biological significance. As research advances, its potential roles in both industry and academia will undoubtedly reveal more about this chemical marvel.
Synonyms
          6-Nitroquinoline
          QUINOLINE, 6-NITRO-
          CCRIS 456
          NSC 4141
          EINECS 210-346-6
          BRN 0136138
          DTXSID1020984
          AI3-08863
          UNII-7033583N3J
          NSC-4141
          NITROQUINOLINE, 6-
          DTXCID70984
          7033583N3J
          5-20-07-00326 (Beilstein Handbook Reference)
          Quinoline, 6nitro
          210-346-6
          inchi=1/c9h6n2o2/c12-11(13)8-3-4-9-7(6-8)2-1-5-10-9/h1-6
          smhplbxivnqfba-uhfffaoysa-n
          613-50-3
          6-Nitro-quinoline
          MFCD00006799
          NSC4141
          6-Nitroquinoline, 98%
          Oprea1_316994
          Oprea1_756562
          SCHEMBL366012
          CHEMBL353078
          BCP27373
          STR06205
          Tox21_200508
          BBL034646
          STL426671
          AKOS000131406
          AC-5110
          CS-W017512
          FN31115
          SB67571
          NCGC00248666-01
          NCGC00258062-01
          CAS-613-50-3
          SY008973
          DB-012204
          N0252
          NS00022499
          EN300-86243
          AC-907/25014227
          AE-842/30168008
          AJ-333/36120006
          SR-01000473458
          SR-01000473458-1
          Q27265819
          F0848-0299
              
Solubility of 6-Nitroquinoline
6-Nitroquinoline, represented by the formula C9H6N2O2, exhibits distinctive solubility properties. Understanding its solubility behavior is essential for applications in various chemical environments. Here are some key points regarding its solubility:
In summary, the solubility of 6-nitroquinoline is influenced by various factors. As a widely studied aromatic compound, its solubility characteristics make it an intriguing subject for further research and application in organic synthesis and medicinal chemistry.