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3-(Diazoniocarbamoyl)pyridine is not a common compound and detailed properties might not be widely available. Below is the chemical formula.

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Identification
Molecular formula
C6H6N4O
CAS number
Not widely available
IUPAC name
3-(diazoniocarbamoyl)pyridine
State
State

At room temperature, 3-(diazoniocarbamoyl)pyridine typically exists in the solid state. This is typical for organic compounds that have a complex nitrogen-based moiety attached to an aromatic ring.

Melting point (Celsius)
0.00
Melting point (Kelvin)
0.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
139.12g/mol
Molar mass
139.1180g/mol
Density
1.2000g/cm3
Appearence

3-(Diazoniocarbamoyl)pyridine typically appears as a colorless to pale yellow crystalline solid. The exact appearance might change slightly depending on the purity of the sample. Solid samples may form agglomerates over time.

Comment on solubility

Solubility of 3-(diazoniocarbamoyl)pyridine

3-(diazoniocarbamoyl)pyridine, with its unique structure, presents interesting solubility characteristics that can be influenced by several factors:

  • Polarity: The presence of the diazonium group contributes to the overall polarity of the molecule, enhancing its ability to interact with polar solvents.
  • Solvent Compatibility: It is generally more soluble in polar solvents such as water and methanol due to hydrogen bonding interactions, whereas its solubility in non-polar solvents is markedly lower.
  • pH Influence: The solubility can also be affected by the pH of the solution. At acidic pH levels, the positively charged diazonium group can enhance solubility, while at neutral or basic pH levels, the solubility might decrease.

In summary, the solubility of 3-(diazoniocarbamoyl)pyridine is primarily influenced by its polarity, the choice of solvent, and environmental factors such as pH. Understanding these aspects is crucial for applications in chemical synthesis and formulation.

Interesting facts

Interesting Facts about 3-(Diazoniocarbamoyl)pyridine

3-(Diazoniocarbamoyl)pyridine is a fascinating compound that showcases the intricate world of nitrogen-containing organic compounds. This compound, characterized by its unique diazoniocarbamoyl group attached to a pyridine ring, presents several noteworthy aspects:

  • Versatility in Synthesis: The presence of multiple reactive functional groups makes this compound a valuable intermediate in synthetic chemistry. It can be utilized in the preparation of various derivatives that possess pharmaceutical and agrochemical importance.
  • Applications in Organic Chemistry: Due to its ability to undergo further transformations, 3-(diazoniocarbamoyl)pyridine frequently finds applications in the development of novel materials and biologically active molecules. This characteristic highlights the importance of diazonium compounds in organic synthesis.
  • Stability and Reactivity: The stability of the compound is primarily attributed to the aromaticity of the pyridine ring. This feature not only enhances its chemical resilience but also influences its reactivity patterns, opening pathways for electrophilic substitution reactions.
  • Research Potential: Scientists continue to explore its potential in various fields, especially in medicinal chemistry where such compounds may exhibit desirable biological activities. For instance, derivatives of this compound might lead to the discovery of new drug candidates.
  • Chemical Education: For students of chemistry, 3-(diazoniocarbamoyl)pyridine serves as an excellent example of the interplay between organic chemistry and coordination complexes, aiding in the understanding of how functional groups interact within molecular frameworks.

In summary, 3-(diazoniocarbamoyl)pyridine is more than just a chemical entity; it is a gateway to numerous possibilities in research and applications. Its unique structure not only embodies the principles of organic chemistry but also inspires innovation in various scientific domains.