N-(2,2-diethoxyethyl)-1-(1,4-dimethyl-9H-carbazol-3-yl)methanimine
ADVERTISEMENT
- Molecular formula
- C22H26N2O2
- CAS Number
- .
- IUPAC Name
- N-(2,2-diethoxyethyl)-1-(1,4-dimethyl-9H-carbazol-3-yl)methanimine
- Molecular Weight
- 342.47g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.1570g/cm3
- Synonyms
- 18073-23-9
Identification
Interesting facts
Interesting Facts about N-(2,2-diethoxyethyl)-1-(1,4-dimethyl-9H-carbazol-3-yl)methanimine
N-(2,2-diethoxyethyl)-1-(1,4-dimethyl-9H-carbazol-3-yl)methanimine is a fascinating compound that showcases intriguing characteristics and potential applications in various fields. Here are some interesting aspects to consider:
- Unique Structure: The compound features a complex structure that combines a carbazole moiety, known for its wide use in organic electronics, with a substituent amine group. This unique architecture can influence its reactivity and properties.
- Potential Applications: Due to the presence of both carbazole and methanimine features, this compound may find applications in:
- Organic light-emitting diodes (OLEDs)
- Photovoltaic cells
- Biological sensing systems
- Carbazole Significance: Carbazole derivatives often exhibit remarkable electronic properties, including:
- High fluorescence efficiency
- Stability under UV light
- Ability to act as hole transport materials in electronic devices
- Reactivity and Synthesis: The introduction of the diethoxyethyl group can enhance the solubility and reactivity of the compound, making it a versatile candidate for further chemical modifications.
- Research Interest: Compounds like this are studied extensively in chemical research, particularly for their potential to develop new materials with tailored properties for emerging technologies.
In summary, N-(2,2-diethoxyethyl)-1-(1,4-dimethyl-9H-carbazol-3-yl)methanimine represents a rich combination of characteristics that are of great interest to chemists and materials scientists alike. Its unique structural features and potential applications highlight the ever-evolving and innovative nature of chemical research.