Interesting facts
Exploring the Fascinating World of 3-Bromoquinoline
3-Bromoquinoline is an intriguing compound that belongs to the class of heterocyclic aromatic compounds. Here are some interesting facts that highlight its significance:
- Quinoline Derivative: As a derivative of quinoline, 3-bromoquinoline contains a nitrogen atom in its bicyclic aromatic structure, which contributes to its chemical reactivity and potential applications.
- Biological Activity: Studies suggest that 3-bromoquinoline exhibits notable biological activities, including antimicrobial and antimalarial properties. This makes it a subject of interest in medicinal chemistry for developing new pharmaceuticals.
- Research Applications: The compound is often used in research to study the interactions of heterocycles with biological systems. Its unique structure allows scientists to probe various chemical pathways and mechanisms.
- Environmental Considerations: Like many brominated compounds, 3-bromoquinoline can be assessed for its environmental impact. Understanding its behavior in ecological systems is crucial due to the potential effects of bromine substitution.
- Versatile Synthesis: There are multiple synthetic pathways to produce 3-bromoquinoline, including bromination reactions of quinoline derivatives. This versatility makes it accessible for laboratory use.
- Flavor and Fragrance: Compounds in the quinoline family are known for their unique scent. Thus, 3-bromoquinoline might find niche applications in the flavor and fragrance industry.
Given its wide-ranging potential and intriguing reactivity, 3-bromoquinoline represents a fascinating area of study for chemists and researchers alike. As the field of medicinal chemistry advances, this compound might become even more relevant in the discovery of new drugs and biological applications.
Synonyms
3-BROMOQUINOLINE
5332-24-1
Quinoline, 3-bromo-
AI3-16560
NSC 3995
EINECS 226-237-1
DTXSID0063787
Quinoline, 3bromo
DTXCID6041399
226-237-1
inchi=1/c9h6brn/c10-8-5-7-3-1-2-4-9(7)11-6-8/h1-6
zgikwinfugeqeo-uhfffaoysa-n
3-Bromo-quinoline
3-Bromoquinliine
MFCD00006767
NSC-3995
3-Bromo quinoline
3-bromoquinolin
3-(bromo)quinoline
3-(bromo) quinoline
Quinolin-3-yl bromide
3-Bromoquinoline, 98%
UPCMLD00WMAL447
ZRP57JF73Z
CHEMBL41490
SCHEMBL271715
NSC3995
STR02922
AKOS005203034
AB00810
AC-2815
CCG-339800
CS-W019978
FB15276
PS-4091
DB-012136
A7761
B1013
NS00032715
EN300-32027
AC-907/25014225
Z337707764
Solubility of 3-Bromoquinoline
3-Bromoquinoline, with the chemical formula C9H6BrN, demonstrates interesting solubility characteristics. This compound is known to be sparingly soluble in water, which is a common trait among many organic compounds that contain aromatic rings. However, its solubility in various organic solvents showcases a more diverse behavior. Key aspects of 3-bromoquinoline's solubility include:
In general, 3-bromoquinoline's solubility characteristics underline the importance of both molecular structure and the solvent environment in determining how compounds behave in various mediums. Understanding these solubility traits is crucial for applications in organic synthesis and related fields, where solubility can greatly impact reaction outcomes.