Interesting facts
Interesting Facts about 2-Chloroethyl-Ethyl-(9H-Fluoren-9-yl)Ammonium Chloride
2-Chloroethyl-Ethyl-(9H-Fluoren-9-yl)Ammonium Chloride is a fascinating compound with significant applications in various fields. Here are some noteworthy points about this intriguing ammonium salt:
- Pharmaceutical Applications: This compound has shown potential in medicinal chemistry, where its unique structure can lead to the development of novel therapeutic agents. The 9H-fluoren-9-yl group is particularly interesting due to its role in enhancing biological activity.
- Ammonium Salts: As an ammonium salt, it exhibits properties typical of quaternary ammonium compounds, which are well-known for their use as disinfectants and surfactants. Its quaternization contributes to its solubility and reactivity, making it a valuable intermediary in organic synthesis.
- Structure-Activity Relationship (SAR): The structure of this compound provides an excellent framework for studying the SAR, where modifications to the fluorenyl moiety or the chloroethyl group can drastically alter the biological activity and selectivity of the resulting compounds.
- Research Significance: Compounds with such complex structures are often subjects of intense research, providing insights into their mechanisms of action and potential applications in drug discovery and development. Scientists are keen to explore how modifications can lead to enhanced efficacy against specific targets.
In summary, 2-Chloroethyl-Ethyl-(9H-Fluoren-9-yl)Ammonium Chloride is much more than just a chemical formula; it represents a bridge between chemistry and real-world applications, illustrating the profound relationships between molecular structure and biological function. As researchers continue to unravel its potential, this compound stands as a testament to the endless possibilities within the realm of chemical research.
Synonyms
2-Chloro-N-(9-fluorenyl)diethylamine hydrochloride
13929-01-6
SKF-501 hydrochloride
Diethylamine, 2-chloro-N-(9-fluorenyl)-, hydrochloride
N-(2-Chloroethyl)-N-ethylfluoren-9-amine hydrochloride
N-(9-Fluorenyl)-N-ethyl-beta-chloroethylamine hydrochloride
9H-Fluoren-9-amine, N-(2-chloroethyl)-N-ethyl-, hydrochloride
FLUOREN-9-AMINE, N-(2-CHLOROETHYL)-N-ETHYL-, HYDROCHLORIDE
Solubility of 2-chloroethyl-ethyl-(9H-fluoren-9-yl)ammonium;chloride
The solubility characteristics of 2-chloroethyl-ethyl-(9H-fluoren-9-yl)ammonium;chloride can be intriguing due to its complex structure. Generally, compounds that contain ammonium groups tend to be more soluble in polar solvents. In this case, the presence of a quaternary ammonium group enhances solubility in water, as such groups can engage in favorable interactions with water molecules.
Key factors influencing its solubility include:
It is often noted that "like dissolves like" which applies here, suggesting that this compound would exhibit better solubility in polar solvents rather than non-polar environments. Optimizing conditions such as temperature and solvent choice can further improve the solubility of this compound.