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3-(4-Butoxy-3-methoxyphenyl)-2-methylprop-2-enhydroxamic acid

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Identification
Molecular formula
C15H21NO4
CAS number
50754-69-5
IUPAC name
3-(4-butoxy-3-methoxy-phenyl)-2-methyl-prop-2-enehydroxamic acid
State
State

At room temperature, 3-(4-Butoxy-3-methoxyphenyl)-2-methylprop-2-enhydroxamic acid is typically a solid. Its state is characterized by its crystalline structure, making it appear as a well-defined powder or crystalline solid.

Melting point (Celsius)
106.00
Melting point (Kelvin)
379.15
Boiling point (Celsius)
355.40
Boiling point (Kelvin)
628.60
General information
Molecular weight
295.34g/mol
Molar mass
295.3500g/mol
Density
1.1560g/cm3
Appearence

3-(4-Butoxy-3-methoxyphenyl)-2-methylprop-2-enhydroxamic acid is typically a crystalline solid. It possesses characteristics dependent largely on its structure and the functional groups present, often appearing as a white or off-white powder.

Comment on solubility

Solubility of 3-(4-butoxy-3-methoxy-phenyl)-2-methyl-prop-2-enehydroxamic acid

The solubility of 3-(4-butoxy-3-methoxy-phenyl)-2-methyl-prop-2-enehydroxamic acid presents a noteworthy discussion due to its complex structure and functional groups. Here are some key points to consider:

  • Polar vs. Nonpolar: The presence of hydroxamic acid groups often introduces significant polarity, which may enhance solubility in polar solvents like water.
  • Hydrogen Bonding: The hydroxamic acid moiety can engage in hydrogen bonding, which potentially increases solubility in various solvents.
  • Alkoxy Groups: The butoxy and methoxy substituents may provide some hydrophobic character, influencing solubility in nonpolar solvents.
  • Overall Solubility: The overall solubility behavior is likely to be a balance between polar and nonpolar interactions, making the compound more soluble in mixed solvent systems.

In summary, solubility is typically multifaceted and influenced by the compound’s functional groups, molecular structure, and the nature of the solvent employed. Thus, while the solubility of 3-(4-butoxy-3-methoxy-phenyl)-2-methyl-prop-2-enehydroxamic acid can be anticipated to be favorable in polar solvents, the presence of hydrophobic alkyl groups plays a critical role in determining its behavior in less polar environments.

Interesting facts

Interesting Facts about 3-(4-butoxy-3-methoxy-phenyl)-2-methyl-prop-2-enehydroxamic acid

The compound 3-(4-butoxy-3-methoxy-phenyl)-2-methyl-prop-2-enehydroxamic acid, often referred to in its shorter name, has garnered interest in the fields of medicinal chemistry and drug development. Here are some key points that highlight its significance:

  • Functional Versatility: This compound features hydroxamic acid functionality, which is known for its ability to form coordination complexes with metal ions. This makes it a candidate for applications in various fields, including biochemical assays.
  • Potential Applications: Hydroxamic acids are often investigated for their antimicrobial and anticancer activities. Research suggests that compounds similar to 3-(4-butoxy-3-methoxy-phenyl)-2-methyl-prop-2-enehydroxamic acid could potentially inhibit certain enzymes, which could be valuable in designing therapeutic agents.
  • Complex Structure: The presence of multiple substituents on the phenyl ring adds complexity and may influence the compound's biological activity. The intriguing arrangement of butoxy and methoxy groups can alter the electronic properties of the molecule.
  • Research Potential: Ongoing research in the field aims to explore and optimize compounds like this one, focusing on modifying its structure for improved efficacy and reduced side effects. As researchers delve deeper into structure-activity relationships, this compound could serve as a significant model.
  • Nature-Inspired Design: The intricate design of this molecule is inspired by natural products and enzyme mechanisms, showcasing the interplay between synthetic chemistry and biological functions.

In summary, 3-(4-butoxy-3-methoxy-phenyl)-2-methyl-prop-2-enehydroxamic acid stands out as a prime example of how structural modifications can synergize to create compounds with potential therapeutic applications. Its study not only expands our understanding of hydroxamic acids but also inspires the continued exploration of novel chemical entities in drug discovery.