Interesting facts
Interesting Facts about 3,4-Dichloro-1-ethyl-pyrrole-2,5-dione
3,4-Dichloro-1-ethyl-pyrrole-2,5-dione is a fascinating compound that continues to capture the interest of chemists and researchers alike due to its unique structure and potential applications. Here are some key points about this compound:
- Unique Structural Features: The incorporation of two chlorine atoms and an ethyl group into the pyrrole ring greatly influences the compound's reactivity and properties. This unique structure can lead to interesting chemical behavior, making it a subject of study for synthetic chemists.
- Biological Significance: Compounds similar to 3,4-dichloro-1-ethyl-pyrrole-2,5-dione may exhibit antimicrobial properties. The exploration of their potential in pharmaceuticals could lead to the development of new antibiotics or antifungal agents.
- Research Potential: Scientists are actively researching pyrrole derivatives because they serve as precursors to various bioactive molecules. Investigating this compound may uncover mechanisms that can be exploited in drug design.
- Environmental Impact: The chlorinated nature of this compound raises interesting questions regarding its environmental behavior and degradation. Understanding its interactions in biological systems and the environment is crucial for assessing its safety and utility in industrial applications.
- Synthetic Pathways: The synthesis of 3,4-dichloro-1-ethyl-pyrrole-2,5-dione often involves multiple reaction steps, highlighting the creativity involved in organic synthesis. Chemists must strategize to minimize by-products and improve yields while maintaining safety in the lab.
In summary, 3,4-dichloro-1-ethyl-pyrrole-2,5-dione is not just another compound in the chemical landscape; it embodies a rich tapestry of research opportunities, biological significance, and synthetic challenges that intrigue both budding chemists and seasoned scientists. As research continues, this compound may reveal even more surprising applications and characteristics.
Synonyms
N-Ethyl-dichloromaleinimide
20198-77-0
MALEIMIDE, 2,3-DICHLORO-N-ETHYL-
2,3-Dichloro-N-ethylmaleimide
VGV0GM54DU
NSC 222506
1H-Pyrrole-2,5-dione, 3,4-dichloro-1-ethyl-
BRN 1527035
3,4-Dichloro-1-ethylmaleimide
NSC-222506
DTXSID80174036
DTXCID9096527
1H-Pyrrole-2,5-dione, 3,4-dichloro-1-ethyl-(9CI)
RefChem:485871
Maleimide, dichloro-N-ethyl-
NSC222506
UNII-VGV0GM54DU
SCHEMBL844833
Maleimide,3-dichloro-N-ethyl-
UNOAAQSLIJPNKG-UHFFFAOYSA-N
AKOS006280155
1H-Pyrrole-2, 3,4-dichloro-1-ethyl-
3,4-dichloro-1-ethyl-1H-pyrrole-2,5-dione
Solubility of 3,4-dichloro-1-ethyl-pyrrole-2,5-dione
3,4-dichloro-1-ethyl-pyrrole-2,5-dione, a complex heterocyclic compound, demonstrates distinct solubility characteristics that are essential for its application in various chemical processes. When considering the solubility of this compound, it is important to note:
In applications where solubility plays a key role, understanding these solvent preferences is crucial. "Like dissolves like" is a fundamental principle here; thus, selecting the appropriate solvent can enhance the efficiency of reactions or extraction methods where 3,4-dichloro-1-ethyl-pyrrole-2,5-dione is involved.
In summary, the solubility of this compound is dictated by its chemical structure and the nature of the solvent, making it vital to choose the right conditions for optimal solubility and reactivity.