Interesting facts
Interesting Facts about 1-(4-Fluorophenyl)-4-(4-methylpiperidin-1-ium-1-yl)butan-1-one; chloride
This intriguing compound, often referred to in studies related to medicinal chemistry, showcases a unique structural configuration that opens the door to various scientific explorations. Below are some key points about this compound:
- Pharmacological Relevance: The presence of the piperidine moiety offers potential in pharmaceutical research, particularly in the development of novel therapeutic agents. Compounds like this one can act as lead structures in drug design.
- Fluorine Chemistry: The 4-fluorophenyl group is known to enhance the lipophilicity of organic molecules, potentially increasing their bioavailability. This characteristic makes such compounds more favorable in medicinal applications.
- Ionization Properties: The piperidin-1-ium substitution highlights the significance of ionic forms in biological systems. The ionic character can affect solubility, membrane permeability, and, ultimately, the pharmacological profile of the compound.
- Analytical Techniques: Techniques such as NMR spectroscopy and mass spectrometry are often employed to study the properties and behavior of compounds like this one, allowing chemists to unveil their structural and electronic attributes.
- Potential Applications: Beyond pharmaceuticals, this compound may find applications in materials science, specifically in developing functional materials through polymerization reactions involving its active groups.
In the realm of chemistry, compounds like 1-(4-fluorophenyl)-4-(4-methylpiperidin-1-ium-1-yl)butan-1-one; chloride serve as valuable platforms for research and innovation, driving forward our understanding of complex molecular interactions.
Synonyms
Buronil
Eunerpan
1-(4-fluorophenyl)-4-(4-methylpiperidin-1-ium-1-yl)butan-1-one;chloride
1-(3-(p-Fluorobenzoyl)propyl)-4-methylpiperazinium chloride
88G640374K
1-[3-(p-fluorobenzoyl)propyl]-4-methylpiperazinium chloride
SCHEMBL1649537
Solubility of 1-(4-fluorophenyl)-4-(4-methylpiperidin-1-ium-1-yl)butan-1-one; chloride
The solubility of the compound 1-(4-fluorophenyl)-4-(4-methylpiperidin-1-ium-1-yl)butan-1-one; chloride is an intriguing aspect of its chemical behavior, primarily influenced by its ionic nature. In general, the chloride salt form tends to exhibit enhanced solubility in polar solvents. Here are some key points to consider:
As a general guideline, one can state emphatically, "like dissolves like." Therefore, exploring a range of solvents will provide a clearer picture of its solubility characteristics. In summary, this compound is expected to be soluble in polar media while exhibiting limited solubility in nonpolar environments due to its ionic nature and structural attributes.