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AH-7921

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Identification
Molecular formula
C20H30ClN3O2
CAS number
55154-30-8
IUPAC name
(2-piperidin-1-ium-1-ylcyclohexyl) N-(2,6-dichlorophenyl)carbamate;chloride
State
State

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

Melting point (Celsius)
174.00
Melting point (Kelvin)
447.15
Boiling point (Celsius)
240.00
Boiling point (Kelvin)
513.15
General information
Molecular weight
384.28g/mol
Molar mass
384.2830g/mol
Density
1.2800g/cm3
Appearence

AH-7921 is typically encountered as a white or off-white crystalline powder, often processed for pharmaceutical research purposes. The powder has a uniform appearance and may be utilized as a hydrochloride salt for research and analytical applications.”

Comment on solubility

Solubility of (2-piperidin-1-ium-1-ylcyclohexyl) N-(2,6-dichlorophenyl)carbamate; chloride

The solubility of this compound is influenced by its structure and the presence of ionic and hydrophobic interactions. Here are key points to consider about its solubility:

  • Ionic Nature: As a chloride salt, the ionic form generally enhances solubility in polar solvents, particularly water.
  • Hydrophobic Groups: The presence of the cyclohexyl group and the dichlorophenyl moiety can introduce hydrophobic characteristics, which may decrease overall solubility in highly polar solvents.
  • Solvent Compatibility: It’s expected to show good solubility in mixed solvents that contain both polar and non-polar characteristics, such as ethanol or methanol.
  • Temperature Dependence: Like many organic compounds, solubility may improve with increased temperatures, affecting its dissolution behavior.

In summary, while (2-piperidin-1-ium-1-ylcyclohexyl) N-(2,6-dichlorophenyl)carbamate; chloride is likely soluble in polar solvents due to its ionic nature, the significant hydrophobic portions of its molecular structure may limit its solubility in pure water. Therefore, the context of the solvent system is crucial for evaluating its solubility.

Interesting facts

Interesting Facts about (2-piperidin-1-ium-1-ylcyclohexyl) N-(2,6-dichlorophenyl)carbamate;chloride

This compound, often referred to by its more simplified name, is a fascinating chemical due to its structure and potential applications. Below are some interesting highlights about this intriguing compound:

  • Complex Structure: The compound features a piperidine ring, which is known for its versatility in organic synthesis. This heterocyclic structure provides unique properties, making it valuable in pharmaceuticals.
  • Potential Biological Activity: The presence of the dichlorophenyl group suggests that this compound may possess notable biological activities. Many derivatives of similar structures are known to exhibit antibacterial, antiviral, or anticancer properties.
  • Chloride Ion Interaction: The chloride component may facilitate interactions with biological targets, impacting the pharmacodynamics of the compound. It also may play a role in enhancing solubility in biological environments, which is crucial for drug formulation.
  • Research Interest: Scientists are keen on exploring its characteristics as part of medicinal chemistry. Investigating the compound could lead to the development of new therapeutic agents or further understand its mechanism of action.
  • Relevant to Drug Design: The design of such compounds emphasizes the significance of modifying functional groups. This approach is vital in designing molecules with improved efficacy and reduced side effects.

As we continue to study the intricacies of compounds like (2-piperidin-1-ium-1-ylcyclohexyl) N-(2,6-dichlorophenyl)carbamate;chloride, we open the door to new discoveries in both chemical synthesis and biological functionality. The intersection of structure and activity in this compound exemplifies the beauty of chemistry.

Synonyms
2,6-Dichlorocarbanilic acid, 2-piperidinocyclohexyl ester hydrochloride
20186-52-1
K 1203
2-Piperidinocyclohexyl 2,6-dichlorocarbanilate hydrochloride
CARBANILIC ACID, 2,6-DICHLORO-, 2-PIPERIDINOCYCLOHEXYL ESTER, HYDROCHLORIDE