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N-(4-styrylphenyl)acetamide

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Identification
Molecular formula
C16H15NO
CAS number
179933-61-0
IUPAC name
N-(4-styrylphenyl)acetamide
State
State

At room temperature, N-(4-styrylphenyl)acetamide is a solid substance. It remains stable under standard conditions, exhibiting its characteristic crystalline form.

Melting point (Celsius)
188.00
Melting point (Kelvin)
461.00
Boiling point (Celsius)
610.00
Boiling point (Kelvin)
883.00
General information
Molecular weight
223.28g/mol
Molar mass
223.2810g/mol
Density
1.1630g/cm3
Appearence

N-(4-styrylphenyl)acetamide appears as an off-white to light yellow crystalline solid. The compound exhibits a fine crystalline morphology.

Comment on solubility

Solubility of N-(4-styrylphenyl)acetamide

N-(4-styrylphenyl)acetamide is a compound that exhibits unique solubility characteristics important for various applications. This compound tends to be sparingly soluble in water, which can be attributed to its organic structure that limits interactions with polar solvents. On the other hand, it shows a much higher solubility in non-polar organic solvents. This behavior can be summarized as follows:

  • Highly Soluble: Non-polar organic solvents such as toluene and chloroform.
  • Sparingly Soluble: Water and other polar solvents.

Factors influencing its solubility include:

  • The presence of the styryl group, which adds hydrophobic character to the molecule.
  • The overall molecular structure that can impact the ability to solvate in certain environments.

It is essential to understand these solubility properties when considering N-(4-styrylphenyl)acetamide for chemical reactions or formulations where solvation plays a crucial role. As a general rule, compounds with higher hydrophobic characteristics will often display better solubility in organic solvents rather than in aqueous solutions.

Interesting facts

Interesting Facts about N-(4-styrylphenyl)acetamide

N-(4-styrylphenyl)acetamide is a fascinating compound that belongs to the class of amides, specifically boasting a phenyl group with a styryl substituent. This structure not only enhances its chemical properties but also contributes to its potential applications in various fields. Here are some noteworthy points:

  • Pharmaceutical Potential: Compounds resembling N-(4-styrylphenyl)acetamide have shown promise in medicinal chemistry. They are often investigated for their potential as analgesics and anti-inflammatory agents, making them relevant in the pursuit of effective pain relief therapies.
  • Fluorescent Properties: The styryl group can impart interesting fluorescent properties, which allow for applications in optical sensors and biomolecular imaging. This versatility is critical in drug discovery and molecular biology research.
  • Structure-Activity Relationship: The unique structural components of this compound facilitate studies on structure-activity relationships (SAR). Researchers can explore how alterations to the phenyl or acetamide groups affect biological activity.
  • Material Science Applications: Beyond medicinal uses, compounds similar to N-(4-styrylphenyl)acetamide can contribute to the development of functional materials. Their ability to undergo polymerization processes makes them suitable for use in creating novel materials.
  • Research Interest: Ongoing research is continuously discovering new functionalities for such compounds, thus attracting attention within the scientific community for its extensive potential.

In summary, N-(4-styrylphenyl)acetamide demonstrates the intricate interplay between structure and function in organic chemistry. Its various applications in fields such as medicine and material science make it a compound worthy of study and appreciation.

Synonyms
N-[4-(2-phenylethenyl)phenyl]acetamide
CBDivE_001873
DTXSID301283951