Interesting facts
Interesting Facts about 6-Dodecyl-2,2,4-trimethyl-1H-quinoline
6-Dodecyl-2,2,4-trimethyl-1H-quinoline is a fascinating organic compound that belongs to the class of quinolines, which are known for their diverse applications in various fields. Here are some intriguing aspects of this compound:
- Structure and Composition: This compound features a complex structure that includes a quinoline ring with an aliphatic dodecyl chain and multiple methyl groups. Such structural characteristics often contribute to its unique physical and chemical properties.
- Biological Activity: Quinolines are renowned for their biological significance, including their role in medicinal chemistry. Many derivatives possess antimalarial, antibacterial, and anti-cancer properties, making the study of compounds like 6-dodecyl-2,2,4-trimethyl-1H-quinoline potentially valuable for pharmaceutical development.
- Applications in Material Science: This compound's unique properties could allow it to be explored for use in organic electronics, such as OLEDs (organic light-emitting diodes) or other optoelectronic applications, highlighting the versatility of quinoline derivatives in modern technology.
- Research Tool: Because of its structural features, this compound can serve as a valuable tool in chemical research, particularly in studies related to synthesis, reactivity patterns, and structure-activity relationships of quinoline derivatives.
- Environmental Fate: Understanding how compounds like 6-dodecyl-2,2,4-trimethyl-1H-quinoline behave in the environment is crucial. Being part of a large class of compounds, its degradation pathways and ecological impacts are significant topics within environmental chemistry.
In conclusion, 6-dodecyl-2,2,4-trimethyl-1H-quinoline exemplifies a compound that straddles the boundaries between organic chemistry, pharmacology, and materials science. Its study not only enhances our understanding of quinoline chemistry but also opens doors to potential applications that could benefit various scientific fields.
Synonyms
6-Dodecyl-1,2-dihydro-2,2,4-trimethylquinoline
89-28-1
SANTOFLEX DD
Quinoline, 6-dodecyl-1,2-dihydro-2,2,4-trimethyl-
HSDB 5265
6-Dodecyl-2,2,4-trimethyl-1,2-dihydroquinoline
EINECS 201-894-7
UNII-UY5F43S7J1
6-dodecyl-2,2,4-trimethyl-1H-quinoline
1,2-DIHYDRO-2,2,4-TRIMETHYL-6-DODECYLQUINOLINE
UY5F43S7J1
DTXSID2052601
1,2-DIHYDRO-6-DODECYL-2,2,4-TRIMETHYLQUINOLINE
1,2-DIHYDRO-2,2,4-TRIMETHYL-6-DODECYLQUINOLINE [HSDB]
SCHEMBL97245
DTXCID6031174
DOFLWDGGNKBGSL-UHFFFAOYSA-N
6Dodecyl1,2dihydro2,2,4trimethylquinoline
6Dodecyl2,2,4trimethyl1,2dihydroquinoline
DB-289503
NS00039318
Quinoline, 6dodecyl1,2dihydro2,2,4trimethyl
6-dodecyl-2,2,4-trimethyl 1,2-dihydroquinoline
Q27291326
Solubility of 6-Dodecyl-2,2,4-trimethyl-1H-quinoline
Understanding the solubility of 6-dodecyl-2,2,4-trimethyl-1H-quinoline is crucial for various applications in chemical formulations and processes. This compound is largely **non-polar** due to the significant size of the dodecyl group, which enhances its hydrophobic characteristics. As a result:
In practical terms, if you need to work with 6-dodecyl-2,2,4-trimethyl-1H-quinoline, consider using organic solvents for dissolving the compound effectively. As the old saying goes, "like dissolves like", emphasizing the principle that polar solvents can dissolve polar solutes, while non-polar solvents are suitable for non-polar solutes.
Overall, the solubility characteristics of this compound make it particularly advantageous in certain chemical formulations, while also presenting challenges in aqueous environments.