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4-Methoxyphenyl-phenyl-diazene

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Identification
Molecular formula
C13H12N2O
CAS number
2418-84-4
IUPAC name
(4-methoxyphenyl)-phenyl-diazene
State
State

At room temperature, 4-Methoxyphenyl-phenyl-diazene is typically found as a solid. It is stable under normal conditions and retains its solid form unless subject to significant temperature increases.

Melting point (Celsius)
134.00
Melting point (Kelvin)
407.15
Boiling point (Celsius)
370.00
Boiling point (Kelvin)
643.15
General information
Molecular weight
213.24g/mol
Molar mass
213.2420g/mol
Density
1.1700g/cm3
Appearence

4-Methoxyphenyl-phenyl-diazene is commonly found in the form of an orange crystalline solid. It exhibits a characteristic deep color typical to azo compounds, which often translates to an orange to red hue in its pure form.

Comment on solubility

Solubility of (4-methoxyphenyl)-phenyl-diazene

The solubility of (4-methoxyphenyl)-phenyl-diazene can be quite intriguing due to its unique structure. Generally, solubility is influenced by a variety of factors including polarity, molecular size, and the presence of functional groups. In the case of (4-methoxyphenyl)-phenyl-diazene, we can observe the following aspects:

  • Polarity: The presence of the methoxy group (-OCH3) increases the overall polarity of the molecule, which may enhance solubility in polar solvents.
  • Molecular Size: As a relatively large organic compound, it may have limited solubility in water, a common solvent.
  • Functional Groups: The -OCH3 group may foster hydrogen bonding interactions, potentially allowing for greater solubility in organic solvents such as ethanol or methanol.

In summary, while (4-methoxyphenyl)-phenyl-diazene likely has low solubility in water due to its steric bulk and hydrophobic characteristics, it may demonstrate enhanced solubility in polar organic solvents. Understanding these solubility characteristics is crucial for applications involving this compound, especially in organic synthesis and material science.

Interesting facts

Interesting Facts about (4-methoxyphenyl)-phenyl-diazene

(4-methoxyphenyl)-phenyl-diazene, often simply referred to by its structural components, presents itself as a fascinating compound in the field of organic chemistry. Here are several key points that make this compound noteworthy:

  • Structure and Functionality: Comprised of a diazene core with two aromatic rings, this compound showcases an interesting interplay of molecular structure that can significantly influence its reactivity.
  • Role in Organic Synthesis: As a diazene derivative, it serves as an important intermediate in various synthetic pathways, particularly in the formation of azo compounds, which are widely used in dyes and pharmaceuticals.
  • Electronics and Photophysics: Compounds similar to (4-methoxyphenyl)-phenyl-diazene exhibit unique electronic properties, making them valuable in the study of photophysics. They can show interesting light absorption and emission characteristics.

Key Reactions: The chemistry of diazenes often includes:

  1. Reduction to hydrazines, which have their own utility in organic synthesis.
  2. Electrophilic Aromatic Substitution can occur, resulting in diverse functionalization of the aromatic rings.

Researchers and students alike find this compound intriguing not just for its theoretical implications but also for its practical applications in materials science and organic electronics. As stated by a noted chemist, "The elegance of a well-designed diazene can open doors to innovation in molecular engineering." The exploration of (4-methoxyphenyl)-phenyl-diazene encourages a deeper investigation into the relationship between structure and function in organic chemistry.

Synonyms
4-Methoxyazobenzene
2396-60-3
EINECS 219-250-9
NSC 16044
219-250-9
1-(4-Methoxyphenyl)-2-phenyldiazene
p-Methoxyazobenzene
(Z)-4-Methoxyazobenzene
Azobenzene, 4-methoxy-
(4-methoxyphenyl)-phenyldiazene
21650-49-7
Diazene, (4-methoxyphenyl)phenyl-
p-Phenylazoanisole
(E)-1-(4-Methoxyphenyl)-2-phenyldiazene
MFCD00039804
15516-72-0
Diazene, (4-methoxyphenyl)phenyl-, (E)-
(4-METHOXYPHENYL)PHENYLDIAZENE
(E)-(4-methoxyphenyl)(phenyl)diazene
(E)-4-Methoxyazobenzene
Azobenzene, 4-methoxy-, (Z)-
p-Methoxyazobenzol
NSC16044
p-Methoxy-cis-azobenzene
Diazene, (4-methoxyphenyl)phenyl-, (Z)-
Anisole, p-(phenylazo)-
4-Methoxyazobenzene, 98%
SCHEMBL1405134
CHEMBL4162540
CHEMBL4177086
Azobenzene, 4-methoxy-, (E)-
DTXSID00870967
4-Methoxyazobenzene, >=99.0%
LGCRPKOHRIXSEG-CCEZHUSRSA-N
LGCRPKOHRIXSEG-PFONDFGASA-N
NSC-16044
AKOS004904015
AKOS016843874
FM10868
1-(4-Methoxyphenyl)-2-phenyldiazene #
AS-62196
LS-14193
SY049428
DB-046304
NS00005397
P0142
(Z)-1-(4-Methoxyphenyl)-2-phenyldiazene #
D91910