Interesting facts
Interesting Facts About Benzyl-(1,7,7-trimethylnorbornan-2-yl)ammonium Chloride
Benzyl-(1,7,7-trimethylnorbornan-2-yl)ammonium chloride is a fascinating compound notable for its unique structure and potential applications. Here are several intriguing aspects of this ammonium salt:
- Quaternary Ammonium Compound: As a quaternary ammonium salt, this compound features four organic groups attached to a nitrogen atom, which enhances its solubility and stability in various environments.
- Role in Organocatalysis: Compounds like this are often used as catalysts in organic synthesis. Their unique properties can facilitate reactions, leading to new chemical transformations and products.
- Biological Applications: Benzyl groups have been found to increase the biological activity of molecules, potentially allowing this compound to be explored in medicinal chemistry for drug design.
- Ion Exchange Properties: The chloride ion in this compound can serve as a counter ion, making it useful in ion exchange processes in various chemical applications.
- Chemical Stability: The presence of the norbornane structure contributes to the presence of a rigid framework that often lends increased stability to the compound compared to more flexible alkylamines.
As you can see, benzyl-(1,7,7-trimethylnorbornan-2-yl)ammonium chloride is a compound with a rich chemistry and a wide array of potential uses. Its distinctive structure not only enhances its reactivity but also opens pathways for further exploration in research and applications.
Synonyms
(+-)-endo-N-Benzyl-2-bornanamine hydrochloride
24652-86-6
2-BORNANAMINE, N-BENZYL-, HYDROCHLORIDE, endo-(+-)-
RefChem:256685
Solubility of Benzyl-(1,7,7-trimethylnorbornan-2-yl)ammonium Chloride
The solubility of benzyl-(1,7,7-trimethylnorbornan-2-yl)ammonium chloride is influenced by several factors, which can be summarized as follows:
However, while it shows promising solubility in polar solvents, its behavior in non-polar solvents is likely to be vastly different, as ionic compounds typically have low solubility in such media. It is essential to visualize solubility as a complex interplay of molecular structure and solvent properties.
In conclusion, the solubility of benzyl-(1,7,7-trimethylnorbornan-2-yl)ammonium chloride is expected to be high in polar solvents, particularly water, due to strong ion-dipole interactions.