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Phenethyl carbamate 2-(1-piperidinyl)ethylamine hydrochloride

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Identification
Molecular formula
C16H26ClN3O2
CAS number
4343-95-1
IUPAC name
2-phenylethyl N-(2-piperidin-1-ium-1-ylethyl)carbamate;chloride
State
State

At room temperature, this compound is generally a solid. It is not highly volatile and remains stable under normal conditions, which is typical for a crystalline organic salt.

Melting point (Celsius)
180.00
Melting point (Kelvin)
453.00
Boiling point (Celsius)
380.50
Boiling point (Kelvin)
653.70
General information
Molecular weight
298.86g/mol
Molar mass
298.8170g/mol
Density
1.1180g/cm3
Appearence

This compound is typically seen in the form of a white or off-white powder. It may also crystallize into small, fine, needle-like formations. The color and crystallinity can be closely attributed to its purity and preparation method.

Comment on solubility

Solubility of 2-phenylethyl N-(2-piperidin-1-ium-1-ylethyl)carbamate;chloride

The solubility of 2-phenylethyl N-(2-piperidin-1-ium-1-ylethyl)carbamate;chloride predominantly depends on the interactions between its molecular structure and the solvent environment. Here are several key points to consider:

  • Polarity: The presence of a quaternary ammonium group suggests a degree of polarity, enhancing potential solubility in polar solvents like water.
  • Hydrophilic Groups: The carbamate functional group is known to participate in hydrogen bonding, further favoring solubility in aqueous environments.
  • Chloride Ion Influence: The chloride ion can facilitate solubility due to its ionic nature, which may enhance the compound's ability to dissociate in polar solvents.

However, it is crucial to note that the actual solubility may vary greatly under different conditions. As a general observation:

  • Temperature: Increased temperature typically improves solubility for many compounds.
  • pH Levels: Changing the pH can influence ionization and, therefore, solubility.

In summary, while 2-phenylethyl N-(2-piperidin-1-ium-1-ylethyl)carbamate;chloride is expected to exhibit notable solubility due to its polar and ionic characteristics, exploring its behavior in varied solvent systems would yield a comprehensive understanding of its solubility profile.

Interesting facts

Interesting Facts about 2-Phenylethyl N-(2-piperidin-1-ium-1-ylethyl)carbamate; Chloride

2-Phenylethyl N-(2-piperidin-1-ium-1-ylethyl)carbamate; chloride is a fascinating compound that bridges organic chemistry and pharmacology. Here are some engaging insights:

  • Dual Roles: This compound acts both as a carbamate and a salt, showcasing properties from both functional groups. Carbamates are known for their applications in pharmaceuticals and agriculture, while the chloride component can enhance solubility and bioavailability.
  • Potential Pharmacological Uses: Compounds with piperidine rings often display significant biological activity. Research into similar structures has led to their use in treating conditions like anxiety and depression, making this compound a promising candidate for further investigation.
  • Synthetic Pathways: The synthesis of this particular carbamate involves intricate organic reactions, often highlighting the importance of protecting groups and selective functionalization. Studying these reactions can enhance our understanding of complex organic synthesis.
  • Structure-Activity Relationship: The functional groups present in the molecule allow for variations that could yield different pharmacological effects. Understanding these relationships can help in designing more effective drugs by tweaking molecular architectures.
  • Interesting Variations: Due to the versatility of the piperidine moiety, researchers might explore derivatives of this compound, potentially leading to the discovery of novel agents or catalysts.

In summary, the intricate structure and potential applications of 2-phenylethyl N-(2-piperidin-1-ium-1-ylethyl)carbamate; chloride make it an intriguing subject for research. As scientist and students continue to unravel its properties, this compound may hold the key to the development of innovative therapeutic agents.

Synonyms
Phenethyl N-(2-piperidinoethyl)carbamate hydrochloride
CARBAMIC ACID, (2-PIPERIDINOETHYL)-, PHENETHYL ESTER, MONOHYDROCHLORIDE
28558-49-8
RefChem:331968