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Morpholinyl Hydroxyphenyl Ethanone

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Identification
Molecular formula
C14H19NO4
CAS number
52934-20-8
IUPAC name
1-[2-hydroxy-4-(2-morpholinoethoxy)phenyl]ethanone
State
State

At room temperature, this compound is in a solid state. It does not have a very high melting point, which makes it amenable to standard chemical manipulation and processing procedures in laboratory settings.

Melting point (Celsius)
97.50
Melting point (Kelvin)
370.60
Boiling point (Celsius)
425.50
Boiling point (Kelvin)
698.60
General information
Molecular weight
265.31g/mol
Molar mass
265.3080g/mol
Density
1.2100g/cm3
Appearence

The compound is typically a crystalline solid. It appears as a white to off-white powder and is mainly used in chemical research applications.

Comment on solubility

Solubility of 1-[2-hydroxy-4-(2-morpholinoethoxy)phenyl]ethanone

The solubility of 1-[2-hydroxy-4-(2-morpholinoethoxy)phenyl]ethanone can be influenced by several factors, including its molecular structure and the presence of functional groups that enhance or hinder solubility.

  • Hydrophilicity: The presence of the hydroxy group introduces polarity, which generally increases solubility in polar solvents like water.
  • Hydrophobic Interactions: The morpholino moiety may contribute to hydrophobic interactions, potentially limiting solubility in aqueous environments while enhancing solubility in organic solvents.
  • Solvent Effects: Common solvents such as ethanol or DMSO may dissolve this compound well due to its amphiphilic character, enabling interactions with both polar and non-polar regions.

In summary, while 1-[2-hydroxy-4-(2-morpholinoethoxy)phenyl]ethanone is expected to exhibit moderate solubility in polar solvents, the exact solubility can vary widely based on the solvent and conditions used. Always refer to empirical data for precise solubility values in specific solvents.

Interesting facts

Interesting Facts about 1-[2-hydroxy-4-(2-morpholinoethoxy)phenyl]ethanone

The compound 1-[2-hydroxy-4-(2-morpholinoethoxy)phenyl]ethanone is a fascinating member of the ketone class of compounds, recognized for its various applications in the field of medicinal chemistry.

Unique Characteristics

  • Structural Complexity: This compound features a phenolic structure that is substituted with both a hydroxyl group and an ethoxy chain attached to a morpholine ring. This unique combination contributes to its diverse biological activity.
  • Therapeutic Potential: Compounds like this one are often investigated for their potential as drug candidates. They may exhibit activity against various diseases, which makes them a subject of interest in pharmaceutical research.
  • Versatile Interactions: The presence of the hydroxyl group allows for hydrogen bonding, enhancing solubility in biological systems and interaction with biological targets.

Applications

This compound has shown promise in various applications:

  • Antioxidant Activity: Some studies suggest that similar compounds possess antioxidant properties, which help in combating oxidative stress in cells.
  • Aids in Drug Design: The morpholine moiety can act as a scaffold for drug development, allowing chemists to modify it for improved efficacy and reduced side effects.
  • Research Tool: Its unique structure makes it valuable for studying receptor interactions and enzyme activities, paving the way for advances in biochemistry.

Scientific Significance

As researchers continue to explore the potential benefits of 1-[2-hydroxy-4-(2-morpholinoethoxy)phenyl]ethanone, its role in the scientific community remains ever-expanding. The compound is a perfect example of how complex structures can lead to groundbreaking discoveries in medicinal chemistry and beyond.

In summary, the investigation of this compound not only deepens our understanding of chemistry but also fortifies the bridge between chemical research and therapeutic advancement.

Synonyms
SCHEMBL23425648