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Dihydroxyaminophenyliminoformamide

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Identification
Molecular formula
C7H9N3O3
CAS number
74373-77-0
IUPAC name
N-[4-(dihydroxyamino)phenyl]iminoformamide
State
State

This compound is typically found in its solid-state at room temperature. It can appear as crystalline or in a powdered form, depending on the conditions of preparation and storage.

Melting point (Celsius)
110.00
Melting point (Kelvin)
383.15
Boiling point (Celsius)
185.00
Boiling point (Kelvin)
458.15
General information
Molecular weight
181.16g/mol
Molar mass
181.1630g/mol
Density
1.2000g/cm3
Appearence

The compound N-[4-(dihydroxyamino)phenyl]iminoformamide typically appears as a solid. The solid form can vary in color depending on purity and specific conditions of its synthesis and storage, but it is usually seen in a crystalline or powdery form.

Comment on solubility

Solubility of N-[4-(dihydroxyamino)phenyl]iminoformamide

N-[4-(dihydroxyamino)phenyl]iminoformamide is a compound that exhibits interesting solubility characteristics. Understanding its solubility is crucial for various applications in chemical processes and formulations.

Solubility Insights

The solubility of this compound can be categorized as follows:

  • Water Solubility: N-[4-(dihydroxyamino)phenyl]iminoformamide is expected to be soluble in water due to the presence of hydroxyl groups which can form hydrogen bonds with water molecules. This property enhances the compound's compatibility with aqueous environments.
  • Solvent Preferences: It is likely that this compound shows variable solubility in organic solvents. Factors influencing this include polarity and intermolecular interactions. For example, it may dissolve well in polar solvents but have limited solubility in non-polar organic solvents.
  • pH Influence: The solubility of N-[4-(dihydroxyamino)phenyl]iminoformamide may also be affected by the pH of the solution. The ionizable groups in the structure can alter solubility at different pH levels, potentially leading to higher solubility in acidic or basic conditions.

In summary, the solubility of N-[4-(dihydroxyamino)phenyl]iminoformamide is a function of several factors, including the polarity of the solvent, the pH level of the solution, and the ability to form hydrogen bonds. Understanding these solubility traits allows for better manipulation and utilization of the compound in various chemical applications.

Interesting facts

Interesting Facts about N-[4-(Dihydroxyamino)phenyl]iminoformamide

The compound N-[4-(dihydroxyamino)phenyl]iminoformamide is an intriguing molecule with a strong connection to various fields including medicinal chemistry and organic synthesis. Here are some noteworthy aspects:

  • Structural Significance: This compound features a unique iminoformamide functional group, which is characterized by its versatility in forming hydrogen bonds. This capability can influence how the molecule interacts with biological systems.
  • Biological Relevance: Compounds with similar structures have been studied for their potential pharmacological activities. They may exhibit properties relevant to anti-cancer or anti-inflammatory agents, making them significant in drug design and development.
  • Hydroxyamino Groups: The presence of dihydroxyamino groups in this compound could modify its reactivity and solubility, impacting its suitability for different biological applications. Such modifications are crucial in optimizing medicinal properties.
  • Synthesis Potential: N-[4-(dihydroxyamino)phenyl]iminoformamide can be synthesized through various organic reactions, providing a platform for students and chemists to explore advanced synthetic techniques in the laboratory.
  • Interdisciplinary Connections: This compound forms a bridge between organic chemistry and biochemistry. Understanding its properties and reactions opens doors to innovative applications in both fields, emphasizing the importance of chemical research.

In conclusion, while N-[4-(dihydroxyamino)phenyl]iminoformamide may not be the most commonly discussed compound, its interesting structural features and biological implications underscore the dynamic nature of chemical research. As stated by renowned chemist Marie Curie, "Nothing in life is to be feared, it is only to be understood." Embracing such compounds allows us to expand our understanding and explore new scientific frontiers.