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2-methyl-4-phenylbutanohydroxamic acid

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Identification
Molecular formula
C11H15NO2
CAS number
56270-44-9
IUPAC name
2-methyl-4-phenyl-butanehydroxamic acid
State
State
At room temperature, it is in the form of a crystalline solid.
Melting point (Celsius)
115.00
Melting point (Kelvin)
388.15
Boiling point (Celsius)
345.00
Boiling point (Kelvin)
618.15
General information
Molecular weight
193.26g/mol
Molar mass
193.2560g/mol
Density
1.1178g/cm3
Appearence

2-Methyl-4-phenylbutanohydroxamic acid typically appears as a crystalline solid. The crystals are usually white or off-white in color, depending on purity.

Comment on solubility

Solubility of 2-methyl-4-phenyl-butanehydroxamic acid

Understanding the solubility of 2-methyl-4-phenyl-butanehydroxamic acid (C11H15NO2) is crucial for its application in various chemical processes. This compound exhibits specific solubility characteristics that can be highlighted:

  • Polar vs. Nonpolar: The presence of the hydroxamic acid functional group introduces polarity, enhancing its solubility in polar solvents.
  • Solvent Compatibility: It tends to be soluble in water and other polar solvents, while its solubility in nonpolar solvents may be limited.
  • Temperature Influence: Like many organic compounds, its solubility can increase with temperature, allowing for more effective dissolution in solutions.
  • pH Dependency: The solubility might vary depending on the pH of the solution, indicating a potential increase in solubility in acidic conditions.

In summary, the solubility of 2-methyl-4-phenyl-butanehydroxamic acid can be influenced by factors such as solvent type, temperature, and pH, making it essential to consider these variables in research and application.

Interesting facts

Interesting Facts about 2-Methyl-4-phenyl-butanehydroxamic Acid

2-Methyl-4-phenyl-butanehydroxamic acid is a fascinating compound that has garnered attention due to its unique chemical structure and potential applications. Here are some intriguing aspects of this compound:

  • Synthetic Utility: Hydroxamic acids are known for their importance in organic synthesis, often serving as intermediates in the development of pharmaceuticals and agrochemicals.
  • Reactivity: The presence of a hydroxamic group in the molecule enhances its reactivity, making it suitable for various reactions, including those involving metal complexes that can catalyze important organic transformations.
  • Biological Significance: Compounds like 2-methyl-4-phenyl-butanehydroxamic acid have been studied for their potential as inhibitors in enzymatic processes, particularly in relation to metalloproteins.
  • History of Hydroxamic Acids: Hydroxamic acids have deep historical roots in medicinal chemistry, with their derivatives being utilized in treatments against bacterial infections, cancer, and other diseases.
  • Research Perspectives: Ongoing research aims to explore the interactions of hydroxamic acids with various biological targets, revealing the potential for novel therapeutic strategies.

In summary, 2-methyl-4-phenyl-butanehydroxamic acid stands out not just for its chemical composition but also for its wide-ranging implications in scientific research and its potential to influence various fields, from pharmaceuticals to materials science. As researchers continue to delve into the capabilities of hydroxamic acids, new and exciting uses for this compound like 2-methyl-4-phenyl-butanehydroxamic acid may emerge, allowing for advancements in drug design and biochemical applications.

Synonyms
MLS000104210
N-hydroxy-2-methyl-4-phenylbutanamide
HDInhib_000072
CBChromo1_000004
Cambridge id 5214063
Oprea1_084837
Oprea1_629878
CBDivE_006593
SCHEMBL8256096
CHEMBL1537941
HMS2413F13
SMR000051259