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3-(3-Chloro-4-propoxyphenyl)prop-2-enehydroxamic acid

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Identification
Molecular formula
C12H14ClNO3
CAS number
943056-75-5
IUPAC name
3-(3-chloro-4-propoxy-phenyl)prop-2-enehydroxamic acid
State
State

At room temperature, 3-(3-Chloro-4-propoxyphenyl)prop-2-enehydroxamic acid is a solid. It is not volatile and does not readily evaporate at normal temperatures."

Melting point (Celsius)
88.50
Melting point (Kelvin)
361.65
Boiling point (Celsius)
595.15
Boiling point (Kelvin)
868.30
General information
Molecular weight
269.70g/mol
Molar mass
269.7100g/mol
Density
1.1800g/cm3
Appearence

3-(3-Chloro-4-propoxyphenyl)prop-2-enehydroxamic acid is typically encountered as a solid. The compound can have a crystalline or powdery appearance, depending on the preparation method and purity. It might exhibit a color ranging from white to off-white."

Comment on solubility

Solubility of 3-(3-chloro-4-propoxy-phenyl)prop-2-enehydroxamic acid

The solubility of 3-(3-chloro-4-propoxy-phenyl)prop-2-enehydroxamic acid in various solvents can provide crucial insights into its chemical behavior and potential applications. Unlike simpler compounds, the solubility of this hydroxamic acid is influenced by several factors:

  • Polarity: The presence of the hydroxamic acid functional group tends to increase polarity, which may enhance solubility in polar solvents such as water or alcohols.
  • Alkyl Substituents: The propoxy group likely results in moderate hydrophobic characteristics, which can affect overall solubility, particularly in non-polar solvents.
  • Temperature: Generally, high temperatures can increase solubility due to enhanced molecular motion, which is particularly relevant for solid compounds.
  • pH Levels: The solubility may vary significantly with changes in pH, as the ionization of the hydroxamic acid can influence solubility in aqueous solutions.

Ultimately, the solubility of 3-(3-chloro-4-propoxy-phenyl)prop-2-enehydroxamic acid is a complex interplay of its molecular structure and the solvent environment. As a result, empirical tests are often necessary to determine the precise solubility characteristics of this compound in practical scenarios. Understanding these aspects is critical for applications in pharmaceuticals and organic synthesis, where solubility impacts reactivity and bioavailability.

Interesting facts

Interesting Facts about 3-(3-chloro-4-propoxy-phenyl)prop-2-enehydroxamic acid

3-(3-chloro-4-propoxy-phenyl)prop-2-enehydroxamic acid is a compound that combines elements of organic chemistry and biochemistry, making it a subject of interest for several research applications. Here are some intriguing aspects of this compound:

  • Chemical Structure: This compound features a unique hydroxyamic acid functional group, which is known for its ability to coordinate with metal ions, enhancing its potential for use in various catalytic processes.
  • Pharmaceutical Applications: Due to the presence of hydroxamic acid, this compound may exhibit *biological activity*, particularly as a potential inhibitor in medicinal chemistry, which can provide insights into drug development and disease treatment.
  • Environmental Significance: Compounds like this one may play a role in bioremediation strategies. The chlorinated phenyl group suggests possible interactions with various biological organisms, paving the way for research into environmental detoxification.
  • Research Interest: The diverse structural groups within this compound offer vast opportunities for chemical modification. Scientists often theorize new derivatives to enhance efficacy or reduce toxicity in potential therapeutic applications.
  • Multi-disciplinary Relevance: This compound spans the fields of organic chemistry, medicinal chemistry, and environmental science, highlighting the interconnectedness of these disciplines and the importance of collaborative research approaches.

As a fascinating example of a complex organic compound, 3-(3-chloro-4-propoxy-phenyl)prop-2-enehydroxamic acid continues to capture the attention of scientists and researchers alike, driving innovations in various scientific fields.