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Caffeic acid dimethylamide

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Identification
Molecular formula
C11H13NO3
CAS number
853275-37-5
IUPAC name
3-(3,4-dimethoxyphenyl)prop-2-enamide
State
State

This compound is a solid at room temperature.

Melting point (Celsius)
115.00
Melting point (Kelvin)
388.15
Boiling point (Celsius)
428.50
Boiling point (Kelvin)
701.65
General information
Molecular weight
207.23g/mol
Molar mass
207.2410g/mol
Density
1.2150g/cm3
Appearence

This compound is typically a crystalline solid. It can appear as a white to off-white powder depending on the specific batch and purity.

Comment on solubility

Solubility of 3-(3,4-dimethoxyphenyl)prop-2-enamide

Understanding the solubility of 3-(3,4-dimethoxyphenyl)prop-2-enamide is crucial for its applications in various fields, including pharmaceuticals and materials science. This compound exhibits noteworthy solubility characteristics:

  • Polar Solvents: It is generally soluble in polar solvents like water, due to the presence of functional groups that can interact favorably with polar molecules.
  • Non-Polar Solvents: The compound is likely to have limited solubility in non-polar solvents; hence, solvents like hexane may not dissolve it well.
  • Temperature Influence: Solubility may increase with temperature, as higher temperatures usually provide sufficient energy to disrupt solute-solvent interactions.
  • pH Dependence: The solubility might also vary with pH, influenced by protonation or deprotonation of functional groups under different acidic or basic conditions.

In summary, the solubility properties of 3-(3,4-dimethoxyphenyl)prop-2-enamide are indicative of its chemical nature, which plays a significant role in its reactivity and functionality. As stated, “Like dissolves like” is a useful motto when predicting how this compound will interact with various solvent systems.

Interesting facts

Exploring 3-(3,4-Dimethoxyphenyl)prop-2-enamide

3-(3,4-Dimethoxyphenyl)prop-2-enamide is a fascinating compound drawing attention in the fields of medicinal chemistry and organic synthesis. As a derivative of prop-2-enamide, this compound exemplifies how structural modifications can influence biological activity and physicochemical properties.

Here are some intriguing facts about this compound:

  • Structural Insights: This compound contains a unique conjugated system, with a double bond and an amide functional group, which are key players in its reactivity and interactions.
  • Biological Relevance: Compounds similar to 3-(3,4-dimethoxyphenyl)prop-2-enamide have been studied for their anti-inflammatory and anticancer properties. This suggests potential therapeutic uses in pharmacology.
  • Synthetic Versatility: The incorporation of dimethoxy groups enhances the compound's synthetic versatility, allowing for various derivatives that can be tailored for specific applications.
  • Research Focus: Ongoing studies into the mechanisms of action of amide compounds indicate that they might interact with specific biological targets, providing insights into novel drug design.

As chemists explore this compound, the pursuit contributes to a greater understanding of how different functional groups can impact the behavior of molecules, leading to innovations in medicinal applications. In the words of renowned chemist, "The beauty of chemistry lies in the infinite number of ways we can combine elements to create something unique."

Overall, 3-(3,4-dimethoxyphenyl)prop-2-enamide serves as a compelling example of the complexity and potential of organic compounds within the realms of science and medicine.

Synonyms
3-(3,4-Dimethoxyphenyl)-2-propenamide
SCHEMBL8153885
SCHEMBL30560923
DTXSID001288683