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Trimethoxycinamic amide

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Identification
Molecular formula
C12H15NO4
CAS number
7268-86-2
IUPAC name
3-(3,4,5-trimethoxyphenyl)prop-2-enamide
State
State

The compound is solid at room temperature.

Melting point (Celsius)
120.50
Melting point (Kelvin)
393.65
Boiling point (Celsius)
452.00
Boiling point (Kelvin)
725.15
General information
Molecular weight
221.25g/mol
Molar mass
221.2450g/mol
Density
1.1230g/cm3
Appearence

3-(3,4,5-Trimethoxyphenyl)prop-2-enamide typically appears as a crystalline solid and can exhibit various shades depending on its purity and formulation. The solid is often white or near-white in appearance.

Comment on solubility

Solubility of 3-(3,4,5-trimethoxyphenyl)prop-2-enamide

The solubility of 3-(3,4,5-trimethoxyphenyl)prop-2-enamide can be influenced by various factors, including its molecular structure and the polarity of the solvent used. Here are some key points regarding its solubility:

  • Polarity: Given the presence of multiple methoxy groups, this compound exhibits a certain degree of polarity. As a result, it is likely to show increased solubility in polar solvents such as water or alcohols.
  • Hydrogen Bonding: The methoxy groups may allow for hydrogen bonding, enhancing solubility in polar environments while reducing solubility in non-polar solvents.
  • Temperature Effects: Solubility can increase with temperature, making it essential to consider temperature conditions during dissolution.
  • Concentration: At higher concentrations, solubility may shift due to saturation effects, impacting how this compound behaves in various solutions.

In summary, while 3-(3,4,5-trimethoxyphenyl)prop-2-enamide is expected to have reasonable solubility in polar solvents, its specific solubility characteristics should be investigated experimentally for accurate and practical applications. As with many organic compounds, solubility can vary widely based on environmental conditions and solvent interactions, making thorough testing crucial for any practical use.

Interesting facts

Exploring 3-(3,4,5-trimethoxyphenyl)prop-2-enamide

3-(3,4,5-trimethoxyphenyl)prop-2-enamide, a fascinating organic compound, is notable for its ___________ properties and diverse applications in the realm of chemistry and medicine. Here are some intriguing facts regarding this compound:

  • Structural Diversity: The compound features a unique structural arrangement with a prop-2-enamide backbone, which contributes to its distinct reactivity and potential interactions.
  • Biological Significance: Derivatives of prop-2-enamide have been studied for their biological activities, including anticancer and anti-inflammatory properties, making them subjects of ongoing research.
  • Synthetic Routes: The synthesis of 3-(3,4,5-trimethoxyphenyl)prop-2-enamide can be achieved through various methods, including nucleophilic additions and condensation reactions. This underscores the compound's versatility in organic synthesis.
  • Chemical Applications: This compound is of interest in pharmacology due to its potential role as a lead compound for drug development, helping chemists discover novel therapeutic agents.
  • Research Potential: Continued exploration may reveal new applications in different fields such as materials science and catalysis, aligning with the nature of many organic compounds to yield multifunctional characteristics.

The beauty of 3-(3,4,5-trimethoxyphenyl)prop-2-enamide lies not only in its complex structure but also in the promises it holds for future discoveries in synthetic organic chemistry. As it stands, it embodies the intersection of creativity and scientific inquiry.

Synonyms
3-(3,4,5-trimethoxyphenyl)prop-2-enamide
DTXSID80859917
NS00123281