Interesting facts
Interesting Facts about 11H-benzocarbazole
11H-benzocarbazole is a fascinating compound with many intriguing aspects that catch the attention of chemists and researchers. Here are some noteworthy points:
- Structure and Origin: This compound belongs to the class of nitrogen-containing polycyclic aromatic hydrocarbons. Its unique structure consists of a fused ring system that includes both a benzene ring and a carbazole moiety.
- Applications in Research: Researchers are particularly interested in 11H-benzocarbazole due to its potential applications in organic electronics and photonics, including its use in devices like organic light-emitting diodes (OLEDs) and solar cells.
- Biological Activity: Studies have shown that 11H-benzocarbazole exhibits interesting biological properties, prompting investigation into its potential as a drug lead compound. Its structure allows for interaction with various biological targets, making it a candidate for further research in pharmacology.
- Environmental Concerns: As a polycyclic aromatic hydrocarbon, 11H-benzocarbazole has raised concerns regarding environmental pollution and its presence in certain combustion processes. Understanding its behavior in the environment is crucial for assessing its ecological impact.
- Synthesis Challenges: The synthesis of 11H-benzocarbazole can be quite complex, typically requiring multiple steps and conditions to achieve purity. This has led to the development of various synthetic methodologies in organic chemistry to simplify its production.
In summary, 11H-benzocarbazole is not just a compound of academic interest; it presents numerous opportunities for advancements in technology and an increased understanding of environmental chemistry. Its potential applications and intriguing properties continue to make it a worthwhile subject of study in the field of organic chemistry.
Synonyms
11H-Benzo[a]carbazole
239-01-0
Benzocarbazole
1,2-Benzocarbazole
1,2-Benzcarbazole
11-Azachrysofluorene
BENZO(A)CARBAZOLE
Benzo[a]carbazole
11H-Benzo(a)carbazole
EINECS 205-945-4
3Y3SPE26QX
NSC 403640
BRN 0155940
MFCD00215939
NSC-60421
NSC-403640
67526-84-5
CHEMBL1173622
C16H11N
5-20-08-00456 (Beilstein Handbook Reference)
WLN: T D6 B566 CMJ
UNII-3Y3SPE26QX
1,2-Benzocarbazole; 11-Azachrysofluorene; Benzo[a]carbazole; NSC 403640; NSC 60421
benzo[1,2]carbazole
benzo[3,4]carbazole
1,2-Benzo-carbazole
11H-?Benzo[a]?carbazole
SCHEMBL70791
11H-benzo[a]carbazole, 99%
DTXSID80946694
NSC60421
BDBM50322599
NSC403640
AKOS024329811
AS-57456
DA-29865
PD179288
SY234275
B4635
CS-0012573
NS00041489
Y10638
Q27258199
205-945-4
Solubility of 11H-benzo[a]carbazole
11H-benzo[a]carbazole, with its complex polycyclic structure, exhibits unique solubility characteristics that warrant attention. The solubility of this compound can be influenced by several factors:
In general, it is observed that "the less polar the solvent, the more soluble 11H-benzo[a]carbazole tends to be." This characteristic is essential for applications in organic synthesis and materials science, where selecting an appropriate solvent can influence the efficacy of reactions and the properties of final products.
In summary, understanding the solubility of 11H-benzo[a]carbazole facilitates its application across various chemical processes and highlights the importance of solvent choice in practical scenarios.