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N-(4-bromophenyl)-2-(diallylamino)acetamide

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Identification
Molecular formula
C14H17BrN2O
CAS number
109383-32-4
IUPAC name
N-(4-bromophenyl)-2-(diallylamino)acetamide
State
State

At room temperature, N-(4-bromophenyl)-2-(diallylamino)acetamide is typically found as a solid. The crystalline structure contributes to its solid state under standard conditions.

Melting point (Celsius)
132.00
Melting point (Kelvin)
405.15
Boiling point (Celsius)
335.50
Boiling point (Kelvin)
608.70
General information
Molecular weight
326.22g/mol
Molar mass
326.2210g/mol
Density
1.4200g/cm3
Appearence

N-(4-bromophenyl)-2-(diallylamino)acetamide is typically a solid at room temperature. It can appear as a white to off-white crystalline powder.

Comment on solubility

Solubility of N-(4-bromophenyl)-2-(diallylamino)acetamide

N-(4-bromophenyl)-2-(diallylamino)acetamide is an intriguing compound when it comes to solubility. Understanding its behavior in different solvents can reveal important information about its chemical properties and potential applications. Here are some key points about its solubility:

  • Polarity: The presence of both a bromophenyl group and a diallylamino group contributes to the overall polarity of the molecule. This suggests that the compound may have a variable solubility in polar and nonpolar solvents.
  • Solvent Compatibility: It is likely to exhibit solubility in organic solvents such as:
    • Dimethyl sulfoxide (DMSO)
    • Ethanol
    • Acetone
  • However, limited solubility may be observed in water due to its hydrophobic aromatic component, which could hinder full dissolution.
  • Temperature Effects: Solubility can also be affected by temperature, typically increasing with higher temperatures for many organic compounds.
  • Predicting Behavior: As a general rule, "like dissolves like." Therefore, the solubility of N-(4-bromophenyl)-2-(diallylamino)acetamide will be enhanced in solvents with similar polarities.

In conclusion, while N-(4-bromophenyl)-2-(diallylamino)acetamide can be expected to dissolve well in compatible organic solvents, its solubility in water is markedly limited. This characteristic makes it an interesting subject for further studies in solubility and potential uses in various chemical applications.

Interesting facts

Exploring N-(4-bromophenyl)-2-(diallylamino)acetamide

N-(4-bromophenyl)-2-(diallylamino)acetamide is a fascinating compound that captures the attention of chemists and researchers alike due to its unique structural attributes and potential applications.

Key Features and Interesting Facts

  • Structural Significance: This compound exhibits a biphenyl structure with the presence of a bromine atom, which significantly influences its reactivity and interaction with biological systems.
  • Potential Applications: Research is ongoing regarding its use in drug development, particularly as it may have significant implications in medicinal chemistry.
  • Biological Interaction: Compounds with similar structures are often investigated for their ability to bind to enzymes and receptors, making them candidates for therapeutic agents.
  • Synthesis Variation: The synthetic routes leading to this compound can vary, and they often incorporate diverse methods that highlight the ingenuity in chemical synthesis.
  • Research Interest: This compound is a subject of study in various disciplines, from organic chemistry to pharmacology, indicating its multifaceted nature.

The chemistry community is continually intrigued by compounds like N-(4-bromophenyl)-2-(diallylamino)acetamide because of their potential to explore new frontiers in drug discovery and development. As stated by a renowned chemist, "The beauty of chemistry lies in the endless possibilities that each new compound presents." This sentiment perfectly captures the spirit of inquiry driving the research into such compounds.

In conclusion, N-(4-bromophenyl)-2-(diallylamino)acetamide serves as a remarkable example of how specific molecular structures can open doors to novel scientific exploration and applications.

Synonyms
4'-Bromo-2-diallylaminoacetanilide
21340-44-3
ACETANILIDE, 4'-BROMO-2-(DIALLYLAMINO)-
BRN 2848708
DTXSID50175611
RefChem:315807
DTXCID8098102