Interesting facts
Interesting Facts about 4,6,7-trimethoxyfuro[2,3-b]quinoline
4,6,7-trimethoxyfuro[2,3-b]quinoline is a fascinating compound that falls within the category of heterocyclic organic compounds. Its unique structure and properties open up a plethora of research opportunities. Here are some noteworthy facts about this intriguing compound:
- Structure and Classification: This compound is part of the quinoline family, characterized by a fused bicyclic structure. Its distinctive furo group adds an additional layer to its complexity and chemical behavior.
- Natural Occurrence: Compounds similar to 4,6,7-trimethoxyfuro[2,3-b]quinoline can be found in various natural sources, particularly in plants known for their medicinal properties.
- Biological Activity: Research has suggested that quinoline derivatives exhibit a wide range of biological activities, including antimicrobial, antiviral, and antitumor properties. The presence of methoxy groups in this compound might enhance its biological efficacy.
- Synthetic Routes: The synthesis of this compound can be approached through several chemical methodologies, showcasing the versatile nature of organic chemistry in generating complex molecules.
- Research Potential: Given its structural characteristics, 4,6,7-trimethoxyfuro[2,3-b]quinoline is a valuable candidate for further pharmacological studies, particularly in drug development for various therapies.
As scientists continue to explore the diverse roles of quinoline derivatives, the future looks promising for 4,6,7-trimethoxyfuro[2,3-b]quinoline in the fields of medicinal chemistry and pharmaceuticals. Its multifaceted nature invites further investigation and could lead to significant advancements in health science.
Synonyms
Kokusaginine
Kokusaginin
484-08-2
4,6,7-Trimethoxyfuro[2,3-b]quinoline
6,7-Dimethoxydictamnine
Dictamnine, 6,7-dimethoxy-
FURO(2,3-b)QUINOLINE, 4,6,7-TRIMETHOXY-
CCRIS 3582
NSC 103013
BRN 0256613
JG1753DK5H
NSC-103013
UNII-JG1753DK5H
DTXSID60197506
4-27-00-02295 (Beilstein Handbook Reference)
Furo[2,3-b]quinoline, 4,6,7-trimethoxy-
4,6,7-TRIMETHOXYFURO(2,3-B)QUINOLINE
DTXCID30119997
jbrxrvfxqikpea-uhfffaoysa-n
CHEBI:6142
CHEMBL278779
Kokusaginine;6,7-Dimethoxydictamnine
Dictamnine,7-dimethoxy-
MLS000574882
MEGxp0_000038
Furo[2, 4,6,7-trimethoxy-
SCHEMBL23870280
HMS2194N12
HMS3328E08
BDBM50098783
NSC103013
AKOS040734863
NCGC00247607-01
4,6,7-Trimethoxy-furo[2,3-b]quinoline
SMR000156276
XK161821
4,6,7-Trimethoxyfuro[2,3-b]quinoline #
DS-011128
HY-114803
CS-0064353
NS00094753
6,7-Dimethoxydictamnine;NSC 103013;Kokusaginine
AC-542/20643020
Q27107100
Solubility of 4,6,7-trimethoxyfuro[2,3-b]quinoline
The solubility of 4,6,7-trimethoxyfuro[2,3-b]quinoline is an intriguing topic, as the compound features a complex structure that influences its interaction with solvents. Its solubility characteristics can be summarized as follows:
It is essential to note that the specific solubility can vary based on factors such as temperature and the presence of other solutes. As a general observation, the solubility of many organic compounds tends to increase with temperature. Therefore, the solubility profile of 4,6,7-trimethoxyfuro[2,3-b]quinoline presents multiple considerations for experimental applications where solvent choice is critical.