Interesting facts
Exploring Quinolin-3-amine
Quinolin-3-amine is an intriguing chemical compound that belongs to the class of heterocyclic aromatic amines, specifically a quinoline derivative. Here are some fascinating facts that highlight its significance in the field of chemistry:
- Structure and Properties: The compound features a fused ring system that contains nitrogen, giving it unique electronic properties and reactivity patterns that are often exploited in organic synthesis.
- Biological Activity: Quinolin-3-amine and its derivatives are known for their potential biological activities. They have been researched for their roles as pharmaceuticals, including antimicrobial and antitumor properties. Such activities make them of particular interest in medicinal chemistry.
- Versatile Syntheses: The synthetic pathways leading to quinolin-3-amine are varied and can involve multiple strategies, such as cyclization reactions and the use of various starting materials. This versatility permits chemists to tailor-make derivatives with desired properties for specific applications.
- Applications in Research: Researchers are continually investigating the utility of quinolin-3-amine in developing fluorescent markers and probes for biological imaging due to its ability to form stable complexes with metal ions.
- Reactivity: The amine group (-NH2) presents interesting reactivity patterns—allowing for further functionalization, which can lead to novel materials and compounds in synthetic organic chemistry.
- Significance in Material Science: Quinoline-based compounds, including quinolin-3-amine, are often studied for their role in the development of organic light-emitting diodes (OLEDs) due to their electronic properties and stability.
In conclusion, quinolin-3-amine is a compound that bridges the fields of organic chemistry, pharmacology, and materials science, marking its importance not just as a molecule of interest but as a cornerstone for advancing multidisciplinary research.
Synonyms
3-AMINOQUINOLINE
quinolin-3-amine
3-Quinolinamine
3-Quinolylamine
Quinoline, 3-amino-
3-Quinolineamine
(Quinolin-3-yl)amine
CCRIS 1678
NSC 7934
EINECS 209-455-1
UNII-98OVL5K3R4
BRN 0113317
98OVL5K3R4
NSC-7934
AMINOQUINOLINE, 3-
DTXSID8060379
5-22-10-00233 (Beilstein Handbook Reference)
DTXCID5042295
inchi=1/c9h8n2/c10-8-5-7-3-1-2-4-9(7)11-6-8/h1-6h,10h
svncrrzkbnsmiv-uhfffaoysa-n
580-17-6
Quinolin-3-ylamine
quinolin-3-yl-amine
MFCD00006772
CHEMBL80298
3-Amino quinoline
3-amino-quinoline
4FS
3-Aminoquinoline, 98%
WLN: T66 BNJ DZ
SCHEMBL14678
BIDD:GT0637
NSC7934
CHEBI:166512
ALBB-008921
BDBM50226051
STK501403
AKOS000321584
FA71740
AC-15004
TS-01881
DB-011137
A0418
NS00015312
EN300-26923
A23340
A869543
AH-034/32464043
Q27272135
F1995-0209
Z234895085
Solubility of Quinolin-3-amine
Quinolin-3-amine, with the chemical formula C9H8N2, demonstrates a unique profile of solubility characteristics essential for a variety of applications. Understanding its solubility is crucial for its effectiveness in different chemical processes.
When discussing the solubility of quinolin-3-amine, consider the following factors:
As a rule of thumb, "like dissolves like," meaning that quinolin-3-amine will likely dissolve more readily in solvents sharing similar polar characteristics. However, testing and empirical data should always be consulted to determine the precise solubility in specific solvents under varying conditions.
In conclusion, the solubility of quinolin-3-amine can significantly affect its behavior in chemical reactions, making it a fascinating subject for further investigation.