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3-(3-ethoxy-4-pentoxyphenyl)prop-2-enehydroxamic acid

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Identification
Molecular formula
C16H23NO4
CAS number
.
IUPAC name
3-(3-ethoxy-4-pentoxy-phenyl)prop-2-enehydroxamic acid
State
State

At room temperature, 3-(3-ethoxy-4-pentoxyphenyl)prop-2-enehydroxamic acid is in a solid state. It is typically maintained in this solid form under standard laboratory conditions, away from moisture and light to ensure its stability.

Melting point (Celsius)
82.00
Melting point (Kelvin)
355.15
Boiling point (Celsius)
325.00
Boiling point (Kelvin)
598.15
General information
Molecular weight
265.32g/mol
Molar mass
265.3200g/mol
Density
1.0530g/cm3
Appearence

3-(3-Ethoxy-4-pentoxyphenyl)prop-2-enehydroxamic acid appears as a white to off-white crystalline solid. The compound may take the form of a fine powder, depending on the preparation and storage conditions. It is typically conserved in a dry environment to prevent the absorption of moisture, which can slightly alter its appearance.

Comment on solubility

Solubility of 3-(3-ethoxy-4-pentoxy-phenyl)prop-2-enehydroxamic acid

The solubility of 3-(3-ethoxy-4-pentoxy-phenyl)prop-2-enehydroxamic acid can be examined through several factors, including its chemical structure and interactions with solvents. This compound, characterized by a hydroxamic acid functional group, can exhibit variable solubility based on its molecular configuration.

Key factors influencing its solubility include:

  • Functional Groups: The presence of the hydroxamic acid group can enhance solubility in polar solvents due to hydrogen bonding capabilities.
  • Hydrophobic Regions: The ethoxy and pentoxy chains contribute hydrophobic characteristics, potentially limiting solubility in water but improving solubility in organic solvents.
  • Temperature: Solubility often increases with temperature, making hot solvents more effective for dissolving this compound.

In general, we can expect the solubility of this compound to be :

  1. Moderate in polar solvents, such as ethanol or methanol, due to the hydroxamic acid functionality.
  2. Higher in non-polar organic solvents, because of the hydrophobic nature of the ethoxy and pentoxy groups.
  3. Lower in water, where the hydrophobic portions dominate, creating less favorable interactions with water molecules.

Careful consideration of these factors will be important when determining the most appropriate solvent for dissolving 3-(3-ethoxy-4-pentoxy-phenyl)prop-2-enehydroxamic acid. Always remember, "the ability to dissolve is as crucial as the chemical reactions that follow."

Interesting facts

Interesting Facts about 3-(3-ethoxy-4-pentoxy-phenyl)prop-2-enehydroxamic acid

3-(3-ethoxy-4-pentoxy-phenyl)prop-2-enehydroxamic acid is a compound notable for its unique structural features and potential applications in various fields of study. Here are some fascinating aspects of this compound:

  • Hydroxamic Acid Functionality: The hydroxamic acid group present in this compound is known to form complexes with metal ions, making it a valuable participant in coordination chemistry.
  • Potential Biological Activity: Compounds with hydroxamic acid moieties have gained attention in medicinal chemistry, particularly for their roles as inhibitors in enzymatic reactions, such as proteases and histone deacetylases.
  • Solvent Interaction: The ethoxy and pentoxy side chains enhance solubility in organic solvents, potentially facilitating their use in various synthetic reactions and applications.
  • Applications in Organic Synthesis: This compound can serve as an intermediate in the synthesis of more complex organic molecules, contributing to fields like pharmaceuticals and agrochemicals.
  • Phenyl Ring Influence: The presence of the phenyl ring can influence the electronic properties of the molecule, affecting its reactivity and interaction with biological targets.

This specific compound exemplifies the intricate balance between structure and function in organic chemistry. As noted by researchers, "the modification of functional groups can profoundly alter the properties and reactivity of organic compounds," highlighting the importance of careful synthesis and design in the development of new materials.

In summary, 3-(3-ethoxy-4-pentoxy-phenyl)prop-2-enehydroxamic acid is a compound rich in potential, particularly in the realms of medicinal chemistry and organic synthesis, making it a subject of ongoing research and exploration.