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AH-7921

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Identification
Molecular formula
C20H29NO3
CAS number
55154-30-8
IUPAC name
[2-(1-piperidyl)cyclohexyl] N-(o-tolyl)carbamate
State
State

At room temperature, AH-7921 exists as a solid.

Melting point (Celsius)
184.00
Melting point (Kelvin)
457.15
Boiling point (Celsius)
440.20
Boiling point (Kelvin)
713.35
General information
Molecular weight
370.50g/mol
Molar mass
370.5030g/mol
Density
1.2100g/cm3
Appearence

AH-7921 typically appears as a white crystalline powder.

Comment on solubility

Solubility of [2-(1-piperidyl)cyclohexyl] N-(o-tolyl)carbamate

The solubility of [2-(1-piperidyl)cyclohexyl] N-(o-tolyl)carbamate can be characterized by various factors that influence its interaction with solvents. This compound is expected to have a notable solubility in organic solvents due to its structure, which contains both polar and non-polar functional groups.

Key Points on Solubility:

  • Solvent Preferences: The presence of the piperidyl and o-tolyl groups suggests solubility in polar organic solvents like ethanol or methanol, and also in non-polar solvents such as hexane.

  • Temperature Influence: Generally, increasing the temperature could improve solubility, allowing the compound to dissolve better in chosen solvents.

  • pH Consideration: The solubility may be further altered by the pH of the solution, particularly if the compound can form ionic species in certain conditions.

In conclusion, the solubility of [2-(1-piperidyl)cyclohexyl] N-(o-tolyl)carbamate primarily depends on the solvent environment and could be enhanced under suitable conditions. As a rule of thumb, “like dissolves like” usually applies, meaning that the molecular interactions between the solvent and compound are crucial for its solubility.

Interesting facts

Interesting Facts about [2-(1-piperidyl)cyclohexyl] N-(o-tolyl)carbamate

[2-(1-piperidyl)cyclohexyl] N-(o-tolyl)carbamate is a fascinating compound in the realm of medicinal chemistry. This compound belongs to a class known as carbamates, which are notable for their presence in various biological applications and their structural diversity. Here are some intriguing aspects of this compound:

  • Synthetic Versatility: The synthesis of this carbamate allows for a wide range of substitutions, making it possible to tailor its properties for specific medicinal purposes.
  • Biological Activity: Compounds like this one have been investigated for their potential pharmacological activities, including neuropharmacological effects. The piperidine ring, in particular, contributes to its ability to interact with neurotransmitter systems.
  • Structure-Activity Relationship: Understanding how the structural components of [2-(1-piperidyl)cyclohexyl] N-(o-tolyl)carbamate influence its biological activity can lead to the development of more effective drugs with fewer side effects.
  • Potential Applications: Research into this compound could reveal uses in the treatment of various neurological disorders. The combination of the cyclohexyl and piperidyl structures may aid in crossing the blood-brain barrier effectively.
  • Importance of Configuration: The spatial arrangement of atoms within this compound can significantly affect its interactions and efficacy, highlighting the importance of stereochemistry in drug design.

As a student or researcher, exploring compounds like [2-(1-piperidyl)cyclohexyl] N-(o-tolyl)carbamate opens exciting avenues for understanding how small changes in molecular architecture can lead to vast differences in biological function. As scientific inquiry continues to advance, the potential of this compound and its derivatives may lead to breakthroughs in therapeutic interventions.