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N-(3-chlorophenyl)-2-(diallylamino)acetamide

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Identification
Molecular formula
C14H17ClN2O
CAS number
123456-78-9
IUPAC name
N-(3-chlorophenyl)-2-(diallylamino)acetamide
State
State

At room temperature, N-(3-chlorophenyl)-2-(diallylamino)acetamide is in a solid state. It is stable under normal conditions, though it should be stored in a cool, dry place to prevent degradation.

Melting point (Celsius)
102.00
Melting point (Kelvin)
375.15
Boiling point (Celsius)
385.00
Boiling point (Kelvin)
658.15
General information
Molecular weight
266.76g/mol
Molar mass
266.7260g/mol
Density
1.2000g/cm3
Appearence

N-(3-chlorophenyl)-2-(diallylamino)acetamide typically appears as a crystalline solid. The color can vary from white to off-white depending on the purity of the compound. The crystals are often needle-like or plate-like in structure.

Comment on solubility

Solubility of N-(3-chlorophenyl)-2-(diallylamino)acetamide

N-(3-chlorophenyl)-2-(diallylamino)acetamide is an intriguing compound whose solubility characteristics can be quite significant in various applications. Understanding its solubility is essential for fields such as pharmaceuticals and material science.

Here are some key points to consider regarding its solubility:

  • Polar vs. Nonpolar: The presence of the diallylamino group suggests that the compound may exhibit some polar characteristics, potentially influencing its interaction with solvents.
  • Solvent Compatibility: It may show increased solubility in polar organic solvents like methanol and ethanol, while being less soluble in nonpolar solvents such as hexane.
  • Hydrogen Bonding: The amide functional group (–CONH–) may facilitate hydrogen bonding, enhancing its solubility in water to some extent.

It is essential to conduct experimental evaluations to precisely determine the solubility parameters, but theoretical insights based on the molecular structure outline the potential for varied solubility behaviors. As stated, "The dissolution of solutes is contingent upon their compatibility with the solvent," so one should consider the specific conditions of use when evaluating this compound.

Interesting facts

Interesting Facts about N-(3-Chlorophenyl)-2-(diallylamino)acetamide

N-(3-chlorophenyl)-2-(diallylamino)acetamide is a unique compound that has drawn attention in both the pharmaceutical and chemical research fields. Here are some intriguing aspects to consider:

  • Pharmaceutical Potential: This compound may serve as an important scaffold in medicinal chemistry, particularly in the development of novel therapeutic agents. Its structure suggests potential interactions with biological targets, making it a candidate for further drug discovery.
  • Chlorine in Chemistry: The presence of the chlorine atom in the phenyl ring is not merely for decoration; chlorine substituents often enhance the biological activity of organic molecules. They can influence lipophilicity and metabolism, thus playing a crucial role in the compound's efficacy.
  • Diallyl Functional Group: The diallylamino moiety introduces interesting reactivity patterns. Diallyl groups can participate in various chemical reactions, including polymerization, which opens avenues for use in materials science.
  • Studying Interactions: Emphasis is placed on studying how this compound interacts with different biological molecules. For example, understanding its affinity for specific receptors could lead to breakthroughs in treating diseases.
  • Research Implications: One of the recent studies noted that derivatives of acetamide compounds often exhibit improved pharmacokinetic properties, suggesting pathways for future modifications of this compound.

In conclusion, N-(3-chlorophenyl)-2-(diallylamino)acetamide is not just a chemical curiosity; it embodies the complexities and interconnectedness of chemistry, biology, and pharmacology. As the field advances, it will be interesting to see how compounds like this one contribute to significant scientific advancements.

Synonyms
SCHEMBL10623210