Interesting facts
Interesting Facts about 2-(2-pyridyl)quinoline-4-carboxylic Acid
2-(2-pyridyl)quinoline-4-carboxylic acid is a fascinating organic compound that belongs to the class of heterocyclic compounds. Here are some intriguing points about this compound:
- Structural Diversity: The compound features a unique combination of a pyridine and quinoline moiety, contributing to its chemical diversity and potential reactivity. This structural relationship enhances its ability to participate in various chemical reactions.
- Biological Significance: Compounds similar to 2-(2-pyridyl)quinoline-4-carboxylic acid have shown potential biological activity. Research indicates that derivatives of this compound can exhibit antimicrobial and anticancer properties, making it a candidate for further medicinal chemistry studies.
- Coordination Chemistry: The presence of both nitrogen atoms in the pyridine and quinoline rings allows this compound to act as a bidentate ligand. It can form complexes with transition metals, which is crucial in numerous industrial and catalytic processes.
- Synthetic Applications: This compound is often utilized in organic synthesis as a building block for more complex molecules. The carboxylic acid functionality enables further derivatization, providing avenues to create functionalized compounds for specific applications.
- Research Tool: Due to its structural features, 2-(2-pyridyl)quinoline-4-carboxylic acid is widely used in research as a probe in studies involving metal-ligand interactions, providing insights into coordination chemistry and molecular recognition.
Overall, 2-(2-pyridyl)quinoline-4-carboxylic acid embodies the intricate interplay between structure and functionality in the realm of organic chemistry, highlighting its importance in both theoretical and applied research.
Synonyms
2-(pyridin-2-yl)quinoline-4-carboxylic acid
673-198-5
57882-27-6
2-Pyridin-2-yl-quinoline-4-carboxylic acid
2-pyridin-2-ylquinoline-4-carboxylic acid
MFCD00224804
CINCHONINIC ACID, 2-(2-PYRIDYL)-
2-(pyridin-2-yl)quinoline-4-carboxylicacid
2-(2-Pyridyl)cinchoninic acid
2-(2-Pyridyl)cinchoninsaeure [German]
2-(2-Pyridyl)-4-quinolinecarboxylic acid
2-(2-pyridyl)quinoline-4-carboxylic acid
Kyselin 2-(2-pyridyl)-cinchoninova [Czech]
4-Quinolinecarboxylic acid, 2-(2-pyridinyl)-
Oprea1_635357
Oprea1_701070
2-(2-Pyridyl)cinchoninsaeure
SCHEMBL7813290
CHEMBL4126356
DTXSID50225887
WSYCFYURDIXHNT-UHFFFAOYSA-N
ALBB-000770
Kyselin 2-(2-pyridyl)-cinchoninova
BBL012184
STK391671
AKOS000114887
TS-7377
NCGC00315957-01
SY063061
2-(2-pyrinyl)-4-Quinolinecarboxylic acid
2-(2-pyridinyl)-4-quinolinecarboxylic acid
2-(2-pyridyl)-quinoline-4-carboxylic acid
2-(2-pyridinyl)-4-quinoline carboxylic acid
EN300-00688
E84016
AB00687152-02
SR-01000213509
SR-01000213509-1
Z56919760
F1981-0006
Solubility of 2-(2-pyridyl)quinoline-4-carboxylic acid
2-(2-pyridyl)quinoline-4-carboxylic acid, with its complex structure, exhibits notable solubility characteristics that can be influenced by various factors. Understanding its solubility is crucial for applications in pharmaceuticals and materials science.
Factors Influencing Solubility
It is often noted that the solubility of such aromatic compounds can be enhanced by the presence of specific functional groups that facilitate hydrogen bonding and dipole interactions. As a result, 2-(2-pyridyl)quinoline-4-carboxylic acid may find its solubility enhanced in the presence of suitable solvent environments.
Conclusion
In summary, the solubility of 2-(2-pyridyl)quinoline-4-carboxylic acid is dictated by its structural features and environmental conditions. Understanding these solubility properties is essential for effective formulation and application in various scientific fields.