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Acetamide azoxybenzene

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Identification
Molecular formula
C14H12N2O2
CAS number
105-13-5
IUPAC name
N-[4-(4-hydroxyphenyl)azophenyl]acetamide
State
State

At room temperature, acetamide azoxybenzene is in a solid state. The crystalline structure is stable under normal atmospheric conditions, but it should be handled with care to avoid exposure to light and moisture, which could potentially alter its composition and physical state.

Melting point (Celsius)
195.00
Melting point (Kelvin)
468.15
Boiling point (Celsius)
379.00
Boiling point (Kelvin)
652.15
General information
Molecular weight
226.26g/mol
Molar mass
226.2380g/mol
Density
1.3547g/cm3
Appearence

Acetamide azoxybenzene appears as an orange-red crystalline solid. It typically forms elongated or needle-like crystals that display a brilliant hue. When exposed to sunlight, the vibrancy of the orange-red coloration can increase due to the inherent photosensitivity of azobenzene derivatives. The compound may also exhibit slight polymorphism, where different crystalline structures can be observed under varying conditions.

Comment on solubility

Solubility of N-[4-(4-hydroxyphenyl)azophenyl]acetamide

N-[4-(4-hydroxyphenyl)azophenyl]acetamide, a compound notable for its complex structure, exhibits intriguing solubility characteristics.

Generally, the solubility of this compound is influenced by a variety of factors, including:

  • Polarity: The presence of both hydroxyl (–OH) and acetamide (–C(O)NH2) functional groups enhances its ability to form hydrogen bonds, which can increase solubility in polar solvents.
  • Temperature: Like many organic compounds, solubility may increase with rising temperature. Hence, heating the solvent can sometimes help dissolve N-[4-(4-hydroxyphenyl)azophenyl]acetamide more effectively.
  • pH Levels: The ionization state of the compound, which can be affected by the pH of the solution, may also play a significant role in determining its solubility.

In practical terms, while it may dissolve well in solvents such as dimethyl sulfoxide (DMSO) or ethanol, its solubility can be limited in non-polar solvents like hexane. It is essential to acknowledge that:

"Solubility is a dynamic property influenced by both the chemical structure and the environment."

In conclusion, understanding the solubility of N-[4-(4-hydroxyphenyl)azophenyl]acetamide not only aids in its effective application but also opens avenues for experimental exploration in various solvent systems.

Interesting facts

Interesting Facts about N-[4-(4-hydroxyphenyl)azophenyl]acetamide

N-[4-(4-hydroxyphenyl)azophenyl]acetamide, commonly referred to as a derivative of azo compounds, is a fascinating chemical entity with a range of applications and properties that excite both researchers and industry professionals. Here are some intriguing facts about this compound:

  • Azo Compounds as Dyes: The azo group (-N=N-) characteristic of this compound plays a crucial role in the dye industry, as many azo compounds are known for their vibrant colors and stability. This particular compound can be explored for use in textile dyes and pigments.
  • Antioxidant Activity: Studies suggest that derivatives of this compound may exhibit antioxidant properties, which could be beneficial in developing health supplements or pharmaceuticals aimed at combating oxidative stress.
  • Pharmaceutical Applications: The acetamide structure contributes to the compound's potential applicability in medicinal chemistry, as modifications to the amide function can lead to new drug candidates for various medical conditions.
  • Research Interest: Due to its unique structure and properties, the compound has attracted attention in academic research, especially concerning its interactions within biological systems and potential mechanisms of action in therapeutic environments.
  • Environmental Considerations: As with many azo compounds, there are concerns regarding environmental persistence and toxicity. Understanding the degradation pathways and effects on ecosystems is crucial for responsible usage.

In summary, N-[4-(4-hydroxyphenyl)azophenyl]acetamide is not just a chemical formula but a gateway to numerous scientific inquiries and industrial applications. Its color, potential health benefits, and role in pharmaceuticals underline the importance of continued research in the realm of chemical compounds.

Synonyms
5302-39-6
N-(4-((4-HYDROXYPHENYL)AZO)PHENYL)ACETAMIDE
327059-75-6
MLS000707634
N-[4-[(4-hydroxyphenyl)diazenyl]phenyl]acetamide
SMR000241627
N-{4-[(4-Hydroxyphenyl)diazenyl]phenyl}acetamide
Acetamide,N-[4-[(4-oxo-2,5-cyclohexadien-1-ylidene)hydrazino]phenyl]-
N-[4-[2-(4-oxocyclohexa-2,5-dien-1-ylidene)hydrazinyl]phenyl]acetamide
CHEMBL1360012
SCHEMBL23259443
4-(4'-acetamidophenylazo)phenol
BDBM49678
cid_5360050
DTXSID70967515
DTXSID301043666
HMS1721N14
HMS2553F05
AKOS001031257
N-[4-[2-(4-oxo-1-cyclohexa-2,5-dienylidene)hydrazinyl]phenyl]acetamide
NCGC00246024-01
SR-01000030257
SR-01000030257-1
Z56801255
N-[4-[N''-(4-ketocyclohexa-2,5-dien-1-ylidene)hydrazino]phenyl]acetamide
N-{4-[2-(4-Oxo-2,5-cyclohexadien-1-ylidene)hydrazinyl]phenyl}acetamide
N-[4-[2-(4-oxidanylidenecyclohexa-2,5-dien-1-ylidene)hydrazinyl]phenyl]ethanamide