Interesting facts
Interesting Facts about 2,3,6-Trichloroquinoxaline
2,3,6-Trichloroquinoxaline is a fascinating compound with several intriguing properties and applications that make it a noteworthy subject of study in the field of chemistry. Here are some compelling points about this compound:
- Structural Insights: As a derivative of quinoxaline, it features a bicyclic structure that consists of a fused benzene ring and a pyrazine ring. This unique arrangement contributes to the compound's distinctive chemical behavior.
- Halogenation Effects: The presence of three chlorine atoms in the molecule not only enhances its reactivity but also alters its electronic properties significantly. Halogens can influence the compound’s ability to participate in various chemical reactions.
- Biological Significance: Compounds like 2,3,6-trichloroquinoxaline are often investigated for their potential as *pharmaceutical intermediates* or their utility in developing biologically active agents. Some studies suggest that derivatives of quinoxaline may exhibit antimicrobial and antitumor activities.
- Research Applications: The compound has been utilized in various research studies focused on understanding its synthetic pathways, properties, and potential uses in fields such as *materials science* and *drug discovery*.
- Environmental Considerations: Due to the chlorinated nature of the compound, it may also attract interest regarding its environmental impact, particularly concerning its breakdown and persistence in ecological systems.
In summary, 2,3,6-trichloroquinoxaline's unique structure and reactivity, alongside its potential applications in pharmaceuticals and environmental studies, make it an essential compound for chemists and researchers alike. Its continuing exploration may unveil further secrets of its capabilities and contributions to science.
Synonyms
2,3,6-Trichloroquinoxaline
2958-87-4
QUINOXALINE, 2,3,6-TRICHLORO-
EINECS 220-987-3
NSC 203052
BRN 0007313
DTXSID7062744
4-23-00-01231 (Beilstein Handbook Reference)
DTXCID7038022
220-987-3
gzegfncrzugiob-uhfffaoysa-n
MFCD00006721
2,3,6-trichloro-quinoxaline
NSC-203052
NSC203052
2,6-Trichloroquinoxaline
Quinoxaline,3,6-trichloro-
SCHEMBL404069
A6A4BK2382
AKOS005074218
2,3,6-Trichloroquinoxaline, AldrichCPR
AC-28117
SY064818
DB-047609
CS-0095259
NS00028729
10E-949
Solubility of 2,3,6-Trichloroquinoxaline
2,3,6-Trichloroquinoxaline, with the chemical formula C8H3Cl3N2, displays intriguing solubility characteristics that are essential for its applications in various chemical processes. Understanding its solubility behavior can provide insights into its interactions in different environments. Here are some key points:
In summary, 2,3,6-trichloroquinoxaline's solubility can be characterized as limited in aqueous environments, making it more compatible with organic solvents, a factor that is critical in both laboratory and industrial applications.