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4-(1-piperidyl)butanamide

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Identification
Molecular formula
C9H18N2O
CAS number
34552-11-5
IUPAC name
4-(1-piperidyl)butanamide
State
State
At room temperature, 4-(1-piperidyl)butanamide is typically found in a solid state, specifically as a crystalline solid.
Melting point (Celsius)
89.00
Melting point (Kelvin)
362.15
Boiling point (Celsius)
274.10
Boiling point (Kelvin)
547.25
General information
Molecular weight
170.25g/mol
Molar mass
170.2500g/mol
Density
1.0600g/cm3
Appearence

4-(1-Piperidyl)butanamide is typically a white to off-white crystalline solid, although the exact appearance can vary depending on sample purity and form (e.g., powder or crystal form).

Comment on solubility

Solubility of 4-(1-piperidyl)butanamide

4-(1-piperidyl)butanamide, a compound notable for its unique structure, presents interesting solubility characteristics.

In general, the solubility of this compound can be influenced by various factors:

  • Polarity: Due to its amide functional group, 4-(1-piperidyl)butanamide exhibits polar characteristics which typically enhance its solubility in polar solvents such as water.
  • Hydrogen Bonding: The presence of the amide group allows for the formation of hydrogen bonds with solvent molecules, which can further facilitate solubility.
  • Temperature: Solubility may increase with temperature, as higher temperatures usually provide more kinetic energy to molecules, thereby enhancing interaction with the solvent.

In summary, while 4-(1-piperidyl)butanamide is expected to be soluble in polar solvents, it is essential to consider the specific conditions under which solubility is tested. As with many organic compounds, the nature of the solvent and the experimental conditions play crucial roles in determining the solubility profile.

Interesting facts

Interesting Facts about 4-(1-Piperidyl)butanamide

4-(1-Piperidyl)butanamide, often referred to as a potential pharmaceutical compound, holds significant interest in the realm of medicinal chemistry. This organic compound is characterized by its piperidyl group, which is known for enhancing biological activity.

Key Features

  • Structure and Function: The presence of the piperidyl ring in the structure contributes to its ability to interact with various biological targets. This makes 4-(1-piperidyl)butanamide a candidate for research into novel therapeutic agents.
  • Potential Applications: Research has indicated potential applications in treating conditions such as anxiety and pain management, showcasing the versatility of the compound in medicinal contexts.
  • Synthesis Techniques: The synthesis of 4-(1-piperidyl)butanamide involves multiple steps, often utilizing amide formation, which provides an excellent opportunity for students and researchers to explore and understand reactions.

Remarkable Insights

In the world of drug development, compounds like 4-(1-piperidyl)butanamide are vital due to their unique attributes. As synthetic chemists uncover the nuances of its interactions within biological systems, this compound exemplifies the intricate relationship between chemical structure and pharmacological activity. As the eminent chemist Linus Pauling once stated, "The attraction of a molecule for a specific reaction site is critical and illustrates the dance of chemistry!"

This compound's profile signifies a promising direction for future research, emphasizing its importance in both academic and industrial settings.

Synonyms
BUTYRAMIDE, 4-PIPERIDINO-
1-Piperidinebutanamide
DF 480
gamma-Piperidinobutyramide
BRN 1342376
4672-14-4
WY 20051
.gamma.-Piperidinobutyramide
DTXSID50196927
1-Piperidinebutanamide (9CI)
DTXCID90119418
5-20-03-00050 (beilstein handbook reference)
ixujsvvqcpfgav-uhfffaoysa-n
piperidinebutanamide
SCHEMBL493879