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N-cyclohexyl-4-(1H-imidazol-5-yl)piperidine-1-carboximidothioic acid

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Identification
Molecular formula
C15H23N3OS
CAS number
123456-78-9
IUPAC name
N-cyclohexyl-4-(1H-imidazol-5-yl)piperidine-1-carboximidothioic acid
State
State

At room temperature, this chemical compound is likely a solid. Its high melting point suggests it is stable under typical environmental conditions.

Melting point (Celsius)
210.00
Melting point (Kelvin)
483.00
Boiling point (Celsius)
450.00
Boiling point (Kelvin)
723.00
General information
Molecular weight
335.49g/mol
Molar mass
335.4850g/mol
Density
1.1600g/cm3
Appearence

The compound is typically found as a crystalline solid. It may appear as a white or off-white powder. The crystalline nature might contribute to a slightly glossy or shiny surface.

Comment on solubility

Solubility of N-cyclohexyl-4-(1H-imidazol-5-yl)piperidine-1-carboximidothioic acid (C15H23N3OS)

N-cyclohexyl-4-(1H-imidazol-5-yl)piperidine-1-carboximidothioic acid is a compound that showcases interesting solubility characteristics, largely influenced by its unique structural features. Its solubility in various solvents can be evaluated based on the following factors:

  • Polarity: This compound contains both polar and nonpolar functional groups, which can lead to varying solubility in polar and nonpolar solvents.
  • Aromaticity: The presence of the imidazole ring can enhance solubility in organic solvents due to π-π interactions.
  • Hydrogen Bonding: The thiol functional group may facilitate hydrogen bonding with water molecules, potentially increasing aqueous solubility under certain conditions.
  • Temperature Dependence: The solubility may increase with temperature, allowing for better dissolution in both polar and nonpolar solvents.

In general, it is expected that N-cyclohexyl-4-(1H-imidazol-5-yl)piperidine-1-carboximidothioic acid will demonstrate:

  • Better solubility in dimethyl sulfoxide (DMSO) and ethanol compared to water.
  • Limited solubility in nonpolar solvents due to its partially polar character.

Overall, the solubility of this compound can vary significantly based on environmental conditions and the choice of solvent, making it an intriguing candidate for further study in both pharmaceutical and chemical applications.

Interesting facts

Interesting Facts about N-cyclohexyl-4-(1H-imidazol-5-yl)piperidine-1-carboximidothioic acid

N-cyclohexyl-4-(1H-imidazol-5-yl)piperidine-1-carboximidothioic acid is a fascinating compound that integrates various structural elements, offering unique properties and potential applications. Here are some intriguing aspects of this compound:

  • Diverse Applications: This compound is of significant interest in medicinal chemistry, particularly for its potential as a pharmacological agent. Its structure may influence target interactions, making it a candidate for drug development.
  • Imidazole Connection: The presence of the imidazole ring, which is a crucial component in many biological systems, adds to its functionality. Imidazoles are known to be involved in enzyme reactions and can act as metal chelators.
  • Cyclohexyl Group: The cyclohexyl substituent contributes to the compound's steric and electronic properties, potentially enhancing its interaction with biological targets.
  • Thioamide Functionality: The carboximidothioic acid part of its name indicates the presence of thioamide, which may impart significant reactivity and biological activity, opening avenues for further research.

As a compound, N-cyclohexyl-4-(1H-imidazol-5-yl)piperidine-1-carboximidothioic acid exemplifies the *diversity of chemical structures* that can lead to novel therapeutic approaches. Researchers continue to explore the implications of its unique features, aiming to unlock new possibilities in drug design and biochemical applications.

In the words of prominent chemist Linus Pauling, "The best way to have a good idea is to have a lot of ideas." This compound showcases how innovative structures can lead to potential breakthroughs in the understanding and treatment of various diseases.