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Paracetamol Allyl Ester

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Identification
Molecular formula
C15H19NO2
CAS number
2580-65-0
IUPAC name
2-(4-acetamidophenyl)-2-allyl-pent-4-enamide
State
State

At room temperature, the compound is in a solid state.

Melting point (Celsius)
151.00
Melting point (Kelvin)
424.15
Boiling point (Celsius)
499.00
Boiling point (Kelvin)
772.15
General information
Molecular weight
245.32g/mol
Molar mass
245.3060g/mol
Density
1.1940g/cm3
Appearence

The compound is typically a crystalline solid, presenting a white or off-white color. It might exhibit a faint odor characteristic of organic chemicals of its nature. The appearance could vary slightly depending on the purity and preparation method.

Comment on solubility

Solubility of 2-(4-acetamidophenyl)-2-allyl-pent-4-enamide

The solubility of 2-(4-acetamidophenyl)-2-allyl-pent-4-enamide in various solvents provides valuable insights into its potential applications and behavior in different environments. Generally speaking, the solubility of organic compounds can be influenced by several factors:

  • Polarity of the Solvent: Compounds with polar functional groups tend to be more soluble in polar solvents such as water, while non-polar or weakly polar compounds show affinity for non-polar solvents like hexane.
  • Temperature: Higher temperatures can increase the solubility of many compounds, allowing more solute to dissolve in a solvent.
  • Hydrogen Bonding: The presence of functional groups capable of hydrogen bonding can enhance solubility in polar solvents. In this case, the acetamide group may facilitate interaction with polar solvents.

Specifically for 2-(4-acetamidophenyl)-2-allyl-pent-4-enamide, its solubility profile may exhibit the following characteristics:

  • It may show moderate solubility in alcohols due to potential hydrogen bonding.
  • However, solubility in water might be limited, given its larger hydrophobic alkyl chain.
  • Acetone and other polar aprotic solvents could also be effective solvents due to their ability to solvate polar functional groups while accommodating hydrophobic regions.

In summary, while predicting solubility can be complex, understanding the structural aspects of 2-(4-acetamidophenyl)-2-allyl-pent-4-enamide can lead to informed estimations about its behavior in various chemical environments. Such insights are crucial for applications in pharmaceuticals, agrochemicals, and materials science.

Interesting facts

Interesting Facts about 2-(4-acetamidophenyl)-2-allyl-pent-4-enamide

2-(4-acetamidophenyl)-2-allyl-pent-4-enamide is a fascinating compound that showcases the intricate connections between chemical structure and biological activity. Here are some intriguing highlights about this compound:

  • Origins in Medicinal Chemistry: This compound, featuring an acetamidophenyl group, is often studied for its potential biological applications, particularly in the realm of pharmaceuticals.
  • Structural Intricacies: The compound's unique structure, which includes both an allyl and a pentenamide group, contributes to its reactivity and interaction with biological systems.
  • Biological Relevance: Compounds of this nature may exhibit various biological properties, such as anti-inflammatory or analgesic effects, making them of considerable interest in drug development.
  • Versatile Reactions: The presence of multiple functional groups allows for a wide range of chemical modifications, driving research in synthetic and medicinal chemistry.
  • Research Applications: Scientists are continuously exploring this compound’s potential as a lead structure for novel therapeutic agents, focusing on how modifications can enhance biological efficacy.

The study of 2-(4-acetamidophenyl)-2-allyl-pent-4-enamide represents a crucial intersection between organic chemistry and biological sciences. As researchers delve into its properties, they continue to uncover the potential that lies within this complex chemical framework.

Synonyms
ACETANILIDE, 4'-(1-ALLYL-1-CARBAMOYL-3-BUTENYL)-
7482-94-2
4'-(1-Allyl-1-carbamoyl-3-butenyl)acetanilide
DTXSID60225792