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AH-7921

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Identification
Molecular formula
C19H28ClN3O2
CAS number
55154-30-8
IUPAC name
(2-piperidin-1-ium-1-ylcyclohexyl) N-(2-chlorophenyl)carbamate;chloride
State
State

This compound is solid at room temperature. It can be found in crystalline or powder form.

Melting point (Celsius)
160.00
Melting point (Kelvin)
433.15
Boiling point (Celsius)
325.00
Boiling point (Kelvin)
598.15
General information
Molecular weight
380.92g/mol
Molar mass
380.9220g/mol
Density
1.2245g/cm3
Appearence

AH-7921 typically appears as a crystalline solid or powder. It may have a white to off-white coloration. The appearance can vary depending on the purity and form of the compound.

Comment on solubility

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:

  • Polar Solvents: The presence of a quaternary ammonium group tends to enhance solubility in polar solvents, particularly in water due to hydrogen bonding capabilities.
  • Nonpolar Solvents: Conversely, its solubility in nonpolar solvents may be limited as these solvents do not effectively interact with ionic parts of the compound.
  • Temperature Effects: Increasing temperature usually increases solubility as the solvation process is facilitated.
  • pH Sensitivity: The solubility might also be affected by the pH of the solution, as changes in pH can alter the ionic state of the compound.

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.

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