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Ethyl Phenylpiracetam

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Identification
Molecular formula
C18H22N2O3
CAS number
77472-70-9
IUPAC name
ethyl 1-(3-amino-3-oxo-propyl)-4-phenyl-piperidine-4-carboxylate
State
State

At room temperature, Ethyl Phenylpiracetam exists as a solid. It is typically stored in a dry environment to maintain its stability.

Melting point (Celsius)
133.00
Melting point (Kelvin)
406.15
Boiling point (Celsius)
342.00
Boiling point (Kelvin)
615.15
General information
Molecular weight
318.39g/mol
Molar mass
318.3890g/mol
Density
1.0530g/cm3
Appearence

The compound appears as a crystalline solid with a white to off-white color. It is fine and powdery in texture.

Comment on solubility

Solubility of Ethyl 1-(3-amino-3-oxo-propyl)-4-phenyl-piperidine-4-carboxylate

The solubility of ethyl 1-(3-amino-3-oxo-propyl)-4-phenyl-piperidine-4-carboxylate is influenced by various factors, particularly its molecular structure and functional groups. Notably, this compound contains both hydrophilic and hydrophobic components, which play a critical role in its solubility behavior.

Factors Influencing Solubility

  • Polarity: The presence of polar groups, such as the carboxylate functional group, enhances the potential for solubility in polar solvents like water.
  • Hydrophobic Characteristics: The phenyl ring contributes to hydrophobic interactions, which may limit solubility in aqueous environments but promote solubility in organic solvents.
  • Hydrogen Bonding: The amino and carboxylate groups can engage in hydrogen bonding, which is beneficial for solubility in both water and alcohols.

As a result, this compound may exhibit:

  • Moderate solubility in polar solvents, particularly due to its hydrophilic groups.
  • Better solubility in organic solvents, given the hydrophobic nature of the phenyl group.

In summary, while ethyl 1-(3-amino-3-oxo-propyl)-4-phenyl-piperidine-4-carboxylate may not be highly soluble in water, it demonstrates a versatile solubility profile depending on the solvent employed. Understanding these solubility dynamics is crucial for applications in pharmaceuticals and organic synthesis.

Interesting facts

Interesting Facts about Ethyl 1-(3-amino-3-oxo-propyl)-4-phenyl-piperidine-4-carboxylate

Ethyl 1-(3-amino-3-oxo-propyl)-4-phenyl-piperidine-4-carboxylate is a fascinating compound that belongs to a class of chemicals known for their diverse biological activities. Here are some noteworthy aspects of this compound:

  • Pharmaceutical Potential: This compound has garnered interest in medicinal chemistry due to its potential as a therapeutic agent. Its structural features suggest the possibility of interaction with various biological targets.
  • Structural Diversity: The combination of a piperidine ring with an attached phenyl group and amino-acid-like features enables a variety of chemical modifications. This diversity can lead to the exploration of a wide range of analogs for enhanced efficacy.
  • Research Applications: Researchers may explore ethyl 1-(3-amino-3-oxo-propyl)-4-phenyl-piperidine-4-carboxylate in fields such as neuropharmacology, where compounds that interact with the central nervous system are of particular interest.
  • Encouraging Further Studies: The compound could serve as a lead compound in drug design, encouraging the development of derivatives that potentially possess improved pharmacological profiles.

Overall, the study of ethyl 1-(3-amino-3-oxo-propyl)-4-phenyl-piperidine-4-carboxylate represents an exciting opportunity within the realm of organic and medicinal chemistry. As researchers delve deeper into its properties and applications, the compound has the potential to inspire innovations in drug development.

Synonyms
CARPERIDINE
7528-13-4
Carperidina
ethyl 1-(3-amino-3-oxopropyl)-4-phenylpiperidine-4-carboxylate
LZ6E4G9827
Carperidinum
Ethyl 1-(2-carbamoylethyl)-4-phenylpiperidine-4-carboxylate
Carperidine [INN:BAN]
7008-32-4
UNII-LZ6E4G9827
Win 13187/2
NIH 7790
CARPERIDINE [INN]
SCHEMBL2107753
CHEMBL2104584
DTXSID10226254
NS00122414
Q5045765
4-Piperidinecarboxylic acid, 1-(3-amino-3-oxopropyl)-4-phenyl-, ethyl ester (9CI); Isonipecotic acid, 1-(2-carbamoylethyl)-4-phenyl-, ethyl ester (8CI); Ethyl 1-(2-carbamoylethyl)-4-phenylpiperidine-4-carboxylate; Carperidine