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Sodium cinnamate N-oxide

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Identification
Molecular formula
C9H8NO2Na
CAS number
.
IUPAC name
sodium;N-oxido-3-phenyl-prop-2-enamide
State
State

At room temperature, sodium cinnamate N-oxide is a solid.

Melting point (Celsius)
140.00
Melting point (Kelvin)
413.15
Boiling point (Celsius)
250.00
Boiling point (Kelvin)
523.00
General information
Molecular weight
172.12g/mol
Molar mass
172.1200g/mol
Density
1.0500g/cm3
Appearence

The compound appears as a white or off-white powder, which is typical of many sodium salts, especially those derived from organic acids or esters.

Comment on solubility

Solubility of Sodium N-Oxido-3-Phenyl-Prop-2-Enamide

Sodium N-oxido-3-phenyl-prop-2-enamide is a compound that exhibits interesting solubility characteristics:

  • Solubility in Water: This compound generally exhibits good solubility in polar solvents like water due to the presence of the sodium ion, which can stabilize interactions with water molecules.
  • Polar vs. Non-Polar Solvents: As a rule of thumb, compounds containing polar functional groups tend to be soluble in polar solvents and less soluble in non-polar solvents.
  • Influence of pH: The solubility of this compound may also vary with the pH of the solution due to the potential ionization of functional groups.
  • Thermal Effects: Temperature changes can affect solubility, with increased temperatures often leading to increased solubility in many compounds.

As a quote from a well-known chemistry text states, "The dissolving process is a balancing act of energy and molecular recognition." It is crucial to consider these factors when predicting the solubility behavior of sodium N-oxido-3-phenyl-prop-2-enamide.

Overall, understanding the solubility of this compound provides valuable insight into its potential applications and interactions in various chemical environments.

Interesting facts

Interesting Facts about Sodium; N-oxido-3-phenyl-prop-2-enamide

N-oxido-3-phenyl-prop-2-enamide, a fascinating compound, is gaining attention in the realm of organic chemistry due to its unique structural features and potential applications. Here are some intriguing aspects worth noting:

  • Structural Diversity: This compound features an N-oxide functional group, which significantly influences its properties and reactivity. The presence of a phenyl ring adds to its aromatic character, potentially impacting its stability and interactions.
  • Reactivity: The N-oxide moiety typically enhances electron density on the nitrogen atom, which can participate in various chemical reactions, including electrophilic substitutions and nucleophilic additions.
  • Applications: N-oxides are known for their roles in medicinal chemistry. They may serve as precursors to pharmaceuticals or be employed in developing agrochemicals, highlighting their relevance in industry.
  • Research Focus: Scientists are exploring this compound's utility in synthesizing more complex molecules. Its elegant structure makes it an ideal candidate for investigations into reaction mechanisms and pathways.
  • Potential Benefits: As researchers work to understand the unique characteristics of N-oxido-3-phenyl-prop-2-enamide, they may uncover new insights that can lead to the creation of innovative materials or drugs tailored for specific applications.

In summary, the study of N-oxido-3-phenyl-prop-2-enamide embodies both the complexity and excitement of modern chemistry. As discoveries unfold, it is essential to keep a keen eye on how this compound could potentially shape future scientific advancements.