Interesting facts
Interesting Facts about 5-Nitroquinoline
5-Nitroquinoline is a fascinating compound with its roots deeply intertwined in the fields of bioorganic chemistry and pharmacology. Here are some intriguing aspects of this compound:
- Structural Features: 5-Nitroquinoline features a nitro group (-NO2) at the 5-position of the quinoline ring. This structural arrangement significantly influences its chemical reactivity and biological activity.
- Biological Applications: Due to its unique structure, 5-Nitroquinoline is often investigated for its antimicrobial and antimalarial properties. The ability of nitro-containing compounds to act as potent antibiotics is well-documented in scientific research.
- Environmental Considerations: Like many nitro compounds, 5-nitroquinoline may pose environmental concerns. Its potential toxicity demands careful handling and thorough assessment of its impact on ecosystems.
- Pharmaceutical Development: The compound has been studied for its role as a lead compound in the design of new pharmaceuticals. Researchers have adapted its structure to synthesize derivatives that could treat a variety of diseases.
- Research Significance: Scientists utilize 5-nitroquinoline in various studies, focusing on reaction mechanisms, charge distribution, and electron-withdrawing properties, which contribute to understanding its reactivity in chemical processes.
In conclusion, 5-nitroquinoline reflects the complexities and utility of nitro compounds in both synthetic and practical applications. Its ongoing study showcases the blend of science and innovation that drives forward modern chemistry and its many real-world applications.
Synonyms
5-Nitroquinoline
607-34-1
QUINOLINE, 5-NITRO-
EINECS 210-134-3
XHP5J23AZ5
NSC 65583
BRN 0135179
NSC-65583
NITROQUINOLINE, 5-
DTXSID8075255
5-20-07-00325 (Beilstein Handbook Reference)
5-(HYDROXYL(OXIDO)AMINO)QUINOLINE
DTXCID1042861
210-134-3
inchi=1/c9h6n2o2/c12-11(13)9-5-1-4-8-7(9)3-2-6-10-8/h1-6
nddzxhocokcnbm-uhfffaoysa-n
5-Nitro-quinoline
MFCD00006790
CHEMBL164449
4lm1
5-Nitroquinoline, 99%
5-Nitro-1-azanaphthalene
UNII-XHP5J23AZ5
NCIOpen2_000225
Oprea1_498855
MLS000516667
SCHEMBL827685
HMS2748I17
NSC65583
BDBM50532268
STL196608
AKOS000280794
AC-2880
CS-W017511
FN15581
PS-4966
SB67468
NCGC00246158-01
BP-21235
SMR000342863
SY003219
DB-000254
N0344
NS00034440
EN300-54168
AC-907/25014226
AF-753/00291046
Q238548
Z56911975
F8889-5729
7ZE
Solubility of 5-nitroquinoline
5-nitroquinoline, with the chemical formula C9H6N2O2, exhibits interesting solubility characteristics influenced by its chemical structure. Understanding its solubility is essential for applications in organic synthesis and pharmaceuticals.
Key Points of Solubility:
In summary, while 5-nitroquinoline displays a degree of solubility in specific organic solvents, it does not readily dissolve in water, making it crucial to carefully select solvent systems when working with this compound. As it is often used in advanced chemical applications, this solubility behavior plays an important role in reaction conditions and product isolation.