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AH-7921

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Identification
Molecular formula
C20H28Cl2N2O2
CAS number
55154-30-8
IUPAC name
[2-(1-piperidyl)cyclohexyl] N-(2,6-dichlorophenyl)carbamate
State
State

At room temperature, AH-7921 is typically in a solid state. It is a synthetic opioid analgesic, used primarily in research settings.

Melting point (Celsius)
183.00
Melting point (Kelvin)
456.15
Boiling point (Celsius)
500.00
Boiling point (Kelvin)
773.15
General information
Molecular weight
379.29g/mol
Molar mass
379.2930g/mol
Density
1.2930g/cm3
Appearence

AH-7921 typically appears as a white powder. It is often found in solid form when synthesized for research or forensic analysis.

Comment on solubility

Solubility of [2-(1-piperidyl)cyclohexyl] N-(2,6-dichlorophenyl)carbamate

The solubility characteristics of [2-(1-piperidyl)cyclohexyl] N-(2,6-dichlorophenyl)carbamate can be quite fascinating due to its unique structural features. This compound, with its complex constitution, exhibits solubility behavior that is influenced by several factors, including:

  • Polarity: The presence of the piperidyl group and carbamate moiety contributes to the overall polar character of the molecule, which can enhance solubility in polar solvents.
  • Hydrophobic Interactions: The cyclohexyl ring adds a hydrophobic segment to the compound, which may lead to limited solubility in highly polar solvents like water.
  • Functional Groups: The 2,6-dichlorophenyl substituent introduces potential for hydrogen bonding, which can impact solubility in certain organic solvents.

When considering solubility, it's essential to note that:

  1. The compound is likely to show higher solubility in organic solvents such as ethanol or dimethyl sulfoxide (DMSO) compared to water.
  2. Temperature can play a significant role, as solubility often increases with an increase in temperature.
  3. Precipitation may occur in less polar solvents, limiting the practical applications in those media.

Overall, while the solubility of [2-(1-piperidyl)cyclohexyl] N-(2,6-dichlorophenyl)carbamate can be understood through its chemical structure, it remains essential to evaluate solubility empirically to determine its behavior in specific conditions and applications.

Interesting facts

Interesting Facts about [2-(1-piperidyl)cyclohexyl] N-(2,6-dichlorophenyl)carbamate

This compound belongs to a class of chemical substances known for their potential therapeutic applications, particularly in the field of neuroscience. Its design incorporates a piperidine ring, which hints at its possible interactions with neurotransmitter receptors, making it a subject of interest for researchers exploring treatments for neurological disorders.

Key Features of the Compound:

  • Structural Diversity: The presence of a piperidyl group attached to a cyclohexyl backbone provides this compound with unique structural properties that can influence its biological activity.
  • Dual Aromatic System: The incorporation of a dichlorophenyl moiety contributes to increased lipophilicity, which can enhance the compound’s ability to cross biological membranes.
  • Potential Applications: Research suggests that compounds with similar structures may exhibit antipsychotic, antidepressant, or analgesic properties, making them valuable in drug design.

As a researcher, delving into the intricate interactions of this compound with various biological targets opens a rich field for exploration. “The more we understand the interplay of structural elements in medicinal chemistry, the better equipped we are to design effective therapeutics,” is a tenet many chemists espouse. Ongoing studies may reveal even more about how subtle changes in a compound’s structure can lead to significant modifications in its pharmacological profile.

In summary, [2-(1-piperidyl)cyclohexyl] N-(2,6-dichlorophenyl)carbamate is not just a chemical structure; it represents a potential pathway toward groundbreaking advancements in medicine and is an exciting subject for both current and future research endeavors.