(9-ethylcarbazol-3-yl)ammonium chloride
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- Molecular formula
- C14H15ClN2
- CAS Number
- 401608-67-7
- IUPAC Name
- (9-ethylcarbazol-3-yl)ammonium;chloride
- Molecular Weight
- 262.76g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2500g/cm3
- Synonyms
- (9-ethylcarbazol-3-yl)azanium, chloride
Identification
Interesting facts
Interesting Facts about (9-ethylcarbazol-3-yl)ammonium;chloride
(9-ethylcarbazol-3-yl)ammonium;chloride is a fascinating compound in the realm of organic and medicinal chemistry. Below are some interesting aspects that highlight its significance:
- Versatile Applications: This compound is widely studied for its potential applications in organic electronics, particularly in light-emitting diodes (OLEDs) and solar cells due to its unique electronic properties.
- Structure and Function: It’s derived from carbazole, a polycyclic aromatic compound that serves as a core structure in many organic materials. The ethyl substituent at the ninth position introduces interesting steric and electronic effects that can be exploited in various chemical reactions.
- Biological Interest: The presence of the ammonium group suggests potential for interactive biological activities, making it a candidate for further research in pharmacology. Compounds like this are often investigated for their ability to modulate biological systems.
- Research and Development: Scientists are keen to study the photophysical properties of (9-ethylcarbazol-3-yl)ammonium;chloride. Its reactivity and stability under different conditions can lead to the development of innovative materials.
In summary, (9-ethylcarbazol-3-yl)ammonium;chloride is not just another compound; it stands at the intersection of physics and chemistry, driving forward advancements in technology and health.