Interesting facts
Interesting Facts about 2-[(2-pyridin-1-ium-1-ylacetyl)amino]ethyl propanoate
2-[(2-pyridin-1-ium-1-ylacetyl)amino]ethyl propanoate is a fascinating organic compound that intersects the realms of medicinal chemistry and biochemistry:
- Structure and Functionality: The compound contains a pyridinium moiety, which is known for its positive charge and unique reactivity. This feature makes it a good candidate for interactions with biological macromolecules.
- Potential Applications: Given its structure, this compound could exhibit interesting biological activities, making it a potential candidate in drug development. Specifically, it could act as a ligand in coordination chemistry or influence various enzymatic activities.
- Research Importance: Compounds that include pyridinic structures have been widely studied due to their roles in various biochemical pathways. Understanding compounds like this one can lead to insights in pharmacology and medicinal chemistry.
- Versatility: The presence of the amino ethyl group enhances its reactivity towards different chemical reactions, allowing it to be modified or conjugated with other functional groups for various applications.
As noted in the field, "Molecular diversity is the key to unlocking new therapeutic strategies." This underscores the significance of compounds like 2-[(2-pyridin-1-ium-1-ylacetyl)amino]ethyl propanoate, which contribute to the development of innovative solutions in medicine.
Overall, this compound exemplifies the intricate relationship between structure and function in organic chemistry, paving the way for future studies and applications in various scientific disciplines.
Solubility of 2-[(2-pyridin-1-ium-1-ylacetyl)amino]ethyl propanoate
The solubility of 2-[(2-pyridin-1-ium-1-ylacetyl)amino]ethyl propanoate is influenced by several key factors:
It is important to note that the specific solvent plays a crucial role in determining the solubility behavior of this compound:
In conclusion, the solubility of 2-[(2-pyridin-1-ium-1-ylacetyl)amino]ethyl propanoate is potentially high in polar environments, influenced by its ionic character and the presence of hydrophilic functional groups.