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Clodronic acid

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Identification
Molecular formula
C10H9ClO3
CAS number
10596-23-3
IUPAC name
4-(4-chlorophenyl)-4-oxo-but-2-enoic acid
State
State

Clodronic acid is typically a solid at room temperature.

Melting point (Celsius)
203.00
Melting point (Kelvin)
476.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
273.15
General information
Molecular weight
260.63g/mol
Molar mass
260.9800g/mol
Density
1.4300g/cm3
Appearence

Clodronic acid appears as a white crystalline powder.

Comment on solubility

Solubility of 4-(4-chlorophenyl)-4-oxo-but-2-enoic acid

The solubility of 4-(4-chlorophenyl)-4-oxo-but-2-enoic acid, also known as a derivative of acrylic acid, can be influenced by a variety of factors. Understanding its solubility characteristics is essential for applications in various chemical processes. Here are some important points regarding its solubility:

  • Polar Character: Due to the presence of the carboxylic acid functional group, this compound exhibits polar characteristics, which often enhance its solubility in polar solvents.
  • Solvent Types: It is generally more soluble in polar protic solvents, such as water and alcohols, compared to non-polar solvents.
  • Hydrogen Bonding: The ability to form hydrogen bonds with solvent molecules can greatly affect its overall solubility, making it more soluble in environments where such interactions are favored.
  • Concentration Effects: In concentrated solutions, the solubility may further change due to interactions between the molecules of the solute.

In summary, the solubility of 4-(4-chlorophenyl)-4-oxo-but-2-enoic acid makes it a compound of interest for diverse applications, particularly in organic synthesis, where its interaction with different solvent mediums can lead to various outcomes. Understanding these solubility characteristics is crucial for optimizing its usage in different chemical contexts.

Interesting facts

Interesting Facts about 4-(4-Chlorophenyl)-4-oxo-but-2-enoic Acid

4-(4-Chlorophenyl)-4-oxo-but-2-enoic acid, often simply referred to in professional circles as a member of the α,β-unsaturated carbonyl compounds, captivates chemists for several compelling reasons:

  • Structure and Stability: This compound features a unique structural framework characterized by a carbonyl group adjacent to a phenyl group. This arrangement contributes to its reactivity and stability, making it a subject of interest for synthetic organic chemistry.
  • Biological Activity: Compounds similar to this one have been explored for their potential biological activities. Researchers investigate their properties in the context of anti-inflammatory and anticancer effects, demonstrating the crucial link between organic chemistry and medicinal applications.
  • Applications in Synthesis: The structural motifs in 4-(4-chlorophenyl)-4-oxo-but-2-enoic acid are often employed as intermediates in organic synthesis, particularly in the fields of pharmaceutical development and materials science. It serves as a valuable building block in the manufacture of various complex molecules.
  • Environmental Relevance: Understanding such compounds is significant given their potential environmental impact. As chlorinated compounds, they require careful handling and study to evaluate their behavior in ecological contexts.

In conclusion, 4-(4-chlorophenyl)-4-oxo-but-2-enoic acid is not just a chemical entity but a compound of significant interest in both academic research and practical applications. As chemists continue to investigate its properties and potential uses, we gain deeper insights into the vast possibilities of organic compounds.

Synonyms
4-(4-chlorophenyl)-4-oxobut-2-enoic acid
SCHEMBL1677880
VQVQEUFKSRHRCT-UHFFFAOYSA-N
3-(4-chlorobenzoyl)-acrylic acid
DTXSID001033973
AKOS030239790
NCI60_012193
4-(4-chlorophenyl)-4-oxo-but-2-enoic acid