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Sodium 4-cyano-2,6-diiodophenolate

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Identification
Molecular formula
C7H3INaNO
CAS number
138786-69-1
IUPAC name
sodium;4-cyano-2,6-diiodo-phenolate
State
State

At room temperature, Sodium 4-cyano-2,6-diiodophenolate exists as a solid. It is relatively stable under standard conditions, making it suitable for various scientific and industrial applications.

Melting point (Celsius)
210.00
Melting point (Kelvin)
483.15
Boiling point (Celsius)
290.00
Boiling point (Kelvin)
563.15
General information
Molecular weight
395.92g/mol
Molar mass
395.9220g/mol
Density
3.0000g/cm3
Appearence

The compound appears as a solid with a crystalline structure, typically characterized by a light yellow to off-white color. The presence of iodine atoms contributes to its heavier and denser nature compared to similar aromatic compounds.

Comment on solubility

Solubility of Sodium 4-Cyano-2,6-Diiodo-Phenolate

The solubility of sodium 4-cyano-2,6-diiodo-phenolate in various solvents can be influenced by several factors, including its ionic nature and the presence of functional groups in its structure. This compound is expected to display varied solubility characteristics:

  • Water: Sodium salts often exhibit good solubility in water due to their ionic nature. The presence of the sodium ion can enhance its solubility, as ionic compounds generally dissociate well in polar solvents.
  • Organic Solvents: Although the presence of halogen substituents (iodine) may decrease solubility in non-polar organic solvents, the cyano group can contribute to solubility in polar organic solvents to some extent.
  • Temperature Effects: As with many compounds, solubility may increase with temperature, allowing for greater dissolution of sodium 4-cyano-2,6-diiodo-phenolate when heated.

In conclusion, while specific solubility data may vary, the compound is likely to be more soluble in polar solvents like water than in non-polar solvents. Understanding these solubility characteristics is crucial for applications in synthesis and analysis.

Interesting facts

Interesting Facts about Sodium 4-Cyano-2,6-Diiodo-Phenolate

Sodium 4-cyano-2,6-diiodo-phenolate is a fascinating compound that showcases the intricate relationship between chemistry and biological applications. Here are some interesting aspects of this compound:

  • Functional Groups: The structure of this compound features a phenolate moiety, which is known for its ability to act as a nucleophile in various chemical reactions.
  • Halogenation Effects: The presence of iodine atoms significantly influences the compound's reactivity, enhancing its ability to participate in electrophilic aromatic substitutions, thus expanding its application in synthetic organic chemistry.
  • Cyanide Group: The cyano group (−C≡N) confers unique electronic properties, allowing for enhanced interactions in biological systems, making this compound a potential candidate for studying enzyme activities.
  • Research Applications: This compound could be useful in designing pharmaceuticals, especially in the areas of anti-cancer or antimicrobial agents, owing to its halogenated aromatic structure.
  • Environmental Impact: The role of phenolic compounds in environmental chemistry is significant, as they often participate in the natural breakdown of pollutants and could contribute to advanced materials in waste remediation.

In summary, sodium 4-cyano-2,6-diiodo-phenolate exemplifies the richness of chemical compounds where structure dictates function, paving the way for numerous applications in science. A quote that resonates with chemists is, "The beauty of chemistry lies in its infinite possibilities." With compounds like this, those possibilities are indeed vast!