6,7-dichloro-1,4-dihydroquinoxaline-2,3-dione
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- Molecular formula
- C8H4Cl2N2O2
- CAS Number
- 2372-66-5
- IUPAC Name
- 6,7-dichloro-1,4-dihydroquinoxaline-2,3-dione
- Molecular Weight
- 245.04g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.6500g/cm3
- Synonyms
- 25983-13-5
Identification
Interesting facts
Interesting Facts about 6,7-Dichloro-1,4-Dihydroquinoxaline-2,3-Dione
6,7-Dichloro-1,4-dihydroquinoxaline-2,3-dione is a fascinating compound that has garnered attention in various fields of research. Here are some intriguing aspects of this chemical:
- Biological Activity: This compound exhibits significant biological properties, making it a subject of interest in pharmaceutical research. It has shown potential as an inhibitory agent against specific enzymes, which could lead to new therapeutic approaches in treating various diseases.
- Synthesis: The synthesis of 6,7-dichloro-1,4-dihydroquinoxaline-2,3-dione involves intricate organic reactions that showcase the versatility of organic chemistry techniques. This includes reactions such as cyclization and chlorination, highlighting the creativity often required in synthetic methodologies.
- Quinoxaline Derivatives: As a member of the quinoxaline family, this compound is closely related to other derivatives that exhibit diverse pharmacological activities. Exploring these derivatives can lead to the discovery of new drugs with enhanced efficacy and safety profiles.
- Research Applications: The compound has been utilized in various scientific studies, particularly in investigating mechanisms of action at the molecular level. Understanding its interactions with biological targets can provide insight into drug design and development.
- Environmental Considerations: As with many chlorinated organic compounds, understanding the environmental impact and degradation pathways of 6,7-dichloro-1,4-dihydroquinoxaline-2,3-dione is crucial. Researchers are actively studying its fate in the environment to ensure safe handling and application.
In summary, 6,7-dichloro-1,4-dihydroquinoxaline-2,3-dione serves as an excellent example of how specific molecular structures can lead to remarkable biological activities. Its versatile synthetic routes and potential applications in drug development make it a compound of continuous interest within the scientific community.