Interesting facts
Interesting Facts about (2-piperidin-1-ium-1-ylcyclohexyl) N-(2-chlorophenyl)carbamate;chloride
This compound, characterized by its complex structure, holds a notable place in pharmacological studies. Here are some intriguing aspects:
- Pharmacological Relevance: This compound is often investigated for its potential therapeutic effects, particularly in the field of neuropharmacology. It may interact with various neurotransmitter systems, making it a candidate for research in treatments for neurological disorders.
- Chlorophenyl Group: The presence of the 2-chlorophenyl group in its structure is significant. Chlorine atoms can enhance the lipophilicity of compounds, potentially improving their bioavailability.
- Piperidine Moiety: The piperidine ring is well-researched in medicinal chemistry. It is known for its ability to act as a base and nucleophile, which makes it an essential component in various synthetic routes to develop new drugs.
- Cyclohexyl Enhancement: The cyclohexyl group contributes to the compound's 3D conformation, which is important for binding to biological targets. The unique spatial arrangement can influence the efficacy and selectivity of the compound.
In summary, the distinct combination of these structural features in (2-piperidin-1-ium-1-ylcyclohexyl) N-(2-chlorophenyl)carbamate;chloride not only piques the interest of researchers but also underscores the intricate relationship between chemical structure and biological function. As scientists continue to explore its properties, this compound may unveil new possibilities in therapeutic development.
Synonyms
o-Chlorocarbanilic acid 2-piperidinocyclohexyl ester hydrochloride
17095-87-3
K 1103
CARBANILIC ACID, o-CHLORO-, 2-PIPERIDINOCYCLOHEXYL ESTER, HYDROCHLORIDE
Solubility of (2-piperidin-1-ium-1-ylcyclohexyl) N-(2-chlorophenyl)carbamate;chloride
The solubility of the compound (2-piperidin-1-ium-1-ylcyclohexyl) N-(2-chlorophenyl)carbamate;chloride can be influenced by various factors such as temperature, pH, and the presence of other solvents. Generally, quaternary ammonium compounds like this one exhibit notable solubility characteristics:
In summary, the solubility of (2-piperidin-1-ium-1-ylcyclohexyl) N-(2-chlorophenyl)carbamate;chloride can be characterized as being highly soluble in polar environments while exhibiting limited solubility in nonpolar media. To maximize solubility, it is crucial to consider the interacting medium and the environmental conditions.