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3-(2,4-dimethoxyphenyl)but-2-enoic acid

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Identification
Molecular formula
C12H14O4
CAS number
65803-41-4
IUPAC name
3-(2,4-dimethoxyphenyl)but-2-enoic acid
State
State

At room temperature, 3-(2,4-dimethoxyphenyl)but-2-enoic acid is typically found in a solid state. This is characteristic of many organic acids, especially aromatic compounds that form stable lattice structures within their crystalline forms.

Melting point (Celsius)
124.00
Melting point (Kelvin)
397.15
Boiling point (Celsius)
360.00
Boiling point (Kelvin)
633.15
General information
Molecular weight
222.25g/mol
Molar mass
222.2470g/mol
Density
1.1200g/cm3
Appearence

The compound 3-(2,4-dimethoxyphenyl)but-2-enoic acid typically appears as a white to off-white crystalline powder. The crystalline nature of the compound can lead to a shiny or slightly glossy texture. The appearance can vary slightly depending on the degree of purity and the method of crystallization used.

Comment on solubility

Solubility of 3-(2,4-dimethoxyphenyl)but-2-enoic acid

3-(2,4-dimethoxyphenyl)but-2-enoic acid, a compound featuring an intriguing aromatic structure, exhibits notable solubility characteristics that are essential for its applications in various fields. Understanding its solubility in different solvents can enhance our comprehension of its functionality:

  • Solvent Polarity: The solubility of this acid is largely influenced by the polarity of the solvent. It tends to be more soluble in polar solvents such as water and alcohol due to the presence of its carboxylic acid group, which can form hydrogen bonds.
  • Aromatic Interactions: The dimethoxy groups impart distinctive aromatic interactions that can also affect solubility. The bulkiness of these groups may limit solubility in highly polar solvents.
  • Temperature Dependency: Like many organic compounds, its solubility can increase with an increase in temperature, allowing for a better dissolution in solvents.
  • pH Sensitivity: This compound’s solubility is greatly influenced by the pH of the solution. Under acidic conditions, the carboxylic acid remains protonated, while at higher pH levels, it can deprotonate, leading to increased solubility.

In summary, the solubility of 3-(2,4-dimethoxyphenyl)but-2-enoic acid is nuanced, governed by factors such as solvent choice, temperature, and pH levels. As always, careful consideration of these variables is crucial for effectively utilizing this compound in practical applications.

Interesting facts

Interesting Facts About 3-(2,4-Dimethoxyphenyl)but-2-enoic Acid

3-(2,4-Dimethoxyphenyl)but-2-enoic acid, also known in some circles for its role in organic synthesis, possesses a fascinating chemical structure that contributes to its unique properties and applications. Let's explore some interesting aspects of this intriguing compound:

  • Versatile Building Block: This compound acts as a versatile building block in the synthesis of more complex organic molecules, showcasing the creativity inherent in organic chemistry.
  • Pharmaceutical Applications: Compounds with similar structures have been investigated for their potential therapeutic effects. Research on related compounds suggests they might exhibit biological activity worth exploring further.
  • Synthetic Chemistry: The methods used to synthesize 3-(2,4-dimethoxyphenyl)but-2-enoic acid often involve strategic use of electrophilic substitution and reduction reactions, which can illuminate students on various organic reagents and techniques.
  • Substituent Effects: The two methoxy groups in the phenyl ring significantly influence both the reactivity and stability of this compound, illustrating the importance of substituent effects in aromatic chemistry.
  • Polar Character: Due to the presence of the carboxylic acid functional group, 3-(2,4-dimethoxyphenyl)but-2-enoic acid exhibits polar characteristics, which are vital for its solubility in different solvents and potential interactions in biological systems.

Moreover, the study of 3-(2,4-dimethoxyphenyl)but-2-enoic acid is not merely an academic exercise. It serves as a reminder of the interplay between structure and function in chemical compounds, which is fundamental to understanding both organic chemistry and its real-world applications. As one researcher aptly stated, “The beauty of chemistry lies in its ability to create endlessly diverse compounds, each with its own story to tell.”


In conclusion, 3-(2,4-dimethoxyphenyl)but-2-enoic acid exemplifies the rich landscape of organic chemistry, where complex structural features give rise to a multitude of opportunities for exploration and discovery.

Synonyms
3-(2,4-Dimethoxyphenyl)-2-butenoic acid
RefChem:490077
SCHEMBL9445631
AKOS030239791
D5047
NS00037878