Skip to main content

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

ADVERTISEMENT
Identification
Molecular formula
C13H15BrN2O
CAS number
151523-53-1
IUPAC name
N-(3-bromophenyl)-2-(diallylamino)acetamide
State
State

At room temperature, it exists in a solid state, usually in the form of a crystalline powder.

Melting point (Celsius)
120.00
Melting point (Kelvin)
393.15
Boiling point (Celsius)
360.00
Boiling point (Kelvin)
633.15
General information
Molecular weight
268.17g/mol
Molar mass
268.1710g/mol
Density
1.2400g/cm3
Appearence

The compound appears as a white to off-white solid, typically observed in a crystalline powder form.

Comment on solubility

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

N-(3-bromophenyl)-2-(diallylamino)acetamide is an intriguing compound that exhibits varying solubility characteristics depending on the solvent used. Understanding its solubility is crucial for applications in medicinal chemistry and material science.

Solubility Characteristics:

  • Polar Solvents: This compound is expected to have moderate solubility in polar solvents such as water and ethanol due to the presence of both amide and amino groups, which can participate in hydrogen bonding.
  • Non-Polar Solvents: Conversely, in non-polar solvents like hexane or benzene, the solubility may be quite low. The significant presence of aromatic and alkyl groups tends to favor non-polar interactions, potentially hindering solubility in polar environments.
  • pH Dependence: The solubility of N-(3-bromophenyl)-2-(diallylamino)acetamide may also be affected by pH levels, with increased solubility in acidic or basic conditions due to ionization effects on the amine group.

In summary, while N-(3-bromophenyl)-2-(diallylamino)acetamide shows promise as a soluble compound in specific situations, it is essential to consider solvent choice and environmental conditions for optimal applications. The interplay between its polarity and molecular structure plays a pivotal role in determining its solubility profile.

Interesting facts

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

N-(3-bromophenyl)-2-(diallylamino)acetamide is a fascinating compound that has garnered attention in the field of organic chemistry and medicinal research. Here are some intriguing aspects worth noting:

  • Pharmacological Potential: This compound exhibits promising bioactive properties, making it a candidate for various therapeutic applications. Its unique structure is believed to interact effectively with biological targets.
  • Structural Significance: The presence of the 3-bromophenyl group plays a crucial role in modifying the electronic properties of the compound, potentially enhancing its reactivity and biological activity.
  • Dual Functionality: The diallylamino component not only contributes to steric and electronic effects but also imparts unique reactivity patterns typical of allies, which can be harnessed for further synthetic modifications.
  • Applications in Drug Design: Compounds like this one can serve as intermediates in the synthesis of more complex molecules, facilitating the discovery of new drugs and expanding our understanding of structure-activity relationships in pharmacology.
  • Research Interests: Ongoing studies focus on its mechanisms of action, especially regarding its potential as an antitumor agent or its effects on enzyme inhibition.

As researchers continue to delve deeper into the characteristics and effects of N-(3-bromophenyl)-2-(diallylamino)acetamide, it holds the promise of contributing significantly to medicinal chemistry and potentially unveiling new avenues for treatment options in the future.

In the words of a prominent chemist: "Innovation in chemistry often lies at the intersection of diverse structures and unexpected functions."