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Acetylaminophenylazophenyldiamine

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Identification
Molecular formula
C14H15N5O
CAS number
6459-94-5
IUPAC name
N-[4-(2,4-diaminophenyl)azophenyl]acetamide
State
State

The compound is solid at room temperature.

Melting point (Celsius)
240.00
Melting point (Kelvin)
513.20
Boiling point (Celsius)
425.20
Boiling point (Kelvin)
698.30
General information
Molecular weight
268.30g/mol
Molar mass
268.3000g/mol
Density
1.2790g/cm3
Appearence

The compound typically appears as a bright yellow to red crystalline powder, indicating its azo structure, which is common in many dyes and pigments.

Comment on solubility

Solubility of N-[4-(2,4-diaminophenyl)azophenyl]acetamide

N-[4-(2,4-diaminophenyl)azophenyl]acetamide exhibits some interesting solubility characteristics worth noting:

  • Solvent Dependence: The solubility of this compound can vary significantly depending on the solvent used. It is generally more soluble in organic solvents such as dimethyl sulfoxide (DMSO) or ethanol compared to water.
  • pH Sensitivity: The solubility may also be influenced by the pH of the solution, with increased solubility noted in more acidic or basic conditions due to protonation/deprotonation effects on the amine groups.
  • Temperature Effects: Higher temperatures tend to enhance the solubility of this compound, leading to a greater dissolution in organic solvents.

It is essential to keep in mind that while N-[4-(2,4-diaminophenyl)azophenyl]acetamide is sparingly soluble in water, its solubility profile can be useful in applications where organic solvents are employed. In practical terms, it is advisable to conduct specific solubility tests under the desired conditions for accurate assessments.

Interesting facts

Interesting Facts about N-[4-(2,4-diaminophenyl)azophenyl]acetamide

N-[4-(2,4-diaminophenyl)azophenyl]acetamide is a fascinating compound that plays a significant role in various fields of chemistry and materials science. Here are some key points that highlight its importance and versatility:

  • Dye Chemistry: This compound is often utilized in the synthesis of azo dyes, which are widely used in textiles and other industries. Azo compounds are known for their vivid colors and stability, making them ideal for dyeing fabrics.
  • Biological Activity: Some derivatives of this compound have been studied for their potential biological activities, including antimicrobial and anticancer effects. This opens avenues for research in pharmaceutical applications.
  • Synthetic Versatility: It serves as an intermediate in organic syntheses, allowing chemists to explore diverse pathways for creating complex molecules. Its structure provides multiple sites for further chemical modification.
  • Research Significance: The azo group present in this compound is a subject of extensive studies in the field of organic chemistry, particularly concerning its reactivity and potential applications in organic electronics and photonic devices.

In the words of a chemist, “The discovery and manipulation of compounds like N-[4-(2,4-diaminophenyl)azophenyl]acetamide not only expand our understanding of dye chemistry but also introduce innovative pathways in drug development and material science.”

This compound serves as a testament to the intricate relationships between chemical structure, function, and application. Its ability to be tuned for specific applications makes it an intriguing area of study for scientists dedicated to exploring new chemical frontiers.

Synonyms
N-(4-((2,4-DIAMINOPHENYL)AZO)PHENYL)ACETAMIDE
18371-12-5