Skip to main content

Ferulamide

ADVERTISEMENT
Identification
Molecular formula
C14H21N3O3
CAS number
13250-05-6
IUPAC name
N-(4-aminobutyl)-3-(4-hydroxy-3-methoxy-phenyl)prop-2-enamide
State
State

Ferulamide is typically a solid at room temperature, often available in crystalline form.

Melting point (Celsius)
215.00
Melting point (Kelvin)
488.15
Boiling point (Celsius)
327.00
Boiling point (Kelvin)
600.15
General information
Molecular weight
235.29g/mol
Molar mass
235.2860g/mol
Density
1.2087g/cm3
Appearence

Ferulamide appears as a light brown crystalline powder.

Comment on solubility

Solubility of N-(4-aminobutyl)-3-(4-hydroxy-3-methoxy-phenyl)prop-2-enamide

N-(4-aminobutyl)-3-(4-hydroxy-3-methoxy-phenyl)prop-2-enamide exhibits distinctive solubility characteristics that can greatly influence its applications in various fields. The solubility of this compound can be attributed to several factors, making it vital to understand:

  • Polarity: With the presence of both hydrophilic (amine and hydroxyl groups) and hydrophobic (aromatic ring) functionalities, this compound may demonstrate moderate solubility in polar solvents such as water.
  • Temperature Dependency: Like many organic compounds, its solubility can vary with temperature. Generally, solubility tends to increase at higher temperatures, which is crucial during synthesis and application.
  • pH Influence: The solubility may also be affected by the pH of the solution, particularly due to the acidic and basic nature of its functional groups. A more alkaline medium might enhance its solubility due to deprotonation of the amino group.
  • Interactions with Solvents: The compound may interact differently with various solvents. Solubility in organic solvents varies, which can lead to specific applications in pharmaceuticals or agrochemicals.

In summary, the solubility of N-(4-aminobutyl)-3-(4-hydroxy-3-methoxy-phenyl)prop-2-enamide is influenced by its unique chemical structure and external conditions. Understanding these properties is essential for optimizing its usage in relevant scientific applications.

Interesting facts

Interesting Facts about N-(4-aminobutyl)-3-(4-hydroxy-3-methoxy-phenyl)prop-2-enamide

This intriguing compound, often referred to as a type of enamide, has garnered attention in various fields of research, particularly in medicinal chemistry and organic synthesis. Here are some captivating insights:

  • Biological Activity: Compounds similar to this one have demonstrated potential as biological agents, exhibiting anti-inflammatory and antioxidant properties. Researchers are exploring its ability to modulate biological pathways, which may lead to new therapeutic applications.
  • Structure-Activity Relationship: The presence of the 4-aminobutyl group and the 4-hydroxy-3-methoxy-phenyl moiety aids in understanding how structural changes influence biological activity. This relationship is crucial in drug design, helping scientists to tailor compounds for improved efficacy.
  • Synthesis Insights: The synthesis of this compound involves various organic reactions, highlighting the versatility of enamine chemistry. Key reactions may include nucleophilic additions and condensation reactions, showcasing how different functional groups can be manipulated in the lab.
  • Research Applications: Ongoing studies aim to assess its potential in fields such as pharmacology and material science. This compound can serve as a foundation for developing novel drugs or materials with unique properties.
  • Impact of Functional Groups: The functional groups within this compound—such as the amine and hydroxyl groups—can greatly affect both solubility and interactions with biological targets, making it a prime candidate for further evaluation in drug discovery.

In summary, N-(4-aminobutyl)-3-(4-hydroxy-3-methoxy-phenyl)prop-2-enamide exemplifies how a single compound can open avenues for research and development across multiple disciplines, contributing to our understanding of chemical interactions and biological implications.

Synonyms
N-(4-aminobutyl)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enamide
SCHEMBL1675877
AKOS028110688
DB-335083