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p-Chlorobenzeneazobenzene

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Identification
Molecular formula
C12H9ClN2
CAS number
495-48-7
IUPAC name
(4-chlorophenyl)-phenyl-diazene
State
State

The compound is a crystalline solid at room temperature, characterized by its vivid color which makes it useful in dyes and pigments.

Melting point (Celsius)
89.00
Melting point (Kelvin)
362.20
Boiling point (Celsius)
365.70
Boiling point (Kelvin)
638.90
General information
Molecular weight
213.67g/mol
Molar mass
213.6440g/mol
Density
1.2091g/cm3
Appearence

The compound typically appears as red to orange-red crystalline solid, which is often used for its intense coloration.

Comment on solubility

Solubility of (4-chlorophenyl)-phenyl-diazene

(4-chlorophenyl)-phenyl-diazene, with the formula C12H10ClN3, is a fascinating compound whose solubility is influenced by its molecular structure and the presence of the chlorophenyl group. Here are some key points regarding its solubility:

  • Solvent Compatibility: This compound is likely to be more soluble in organic solvents such as ethanol, acetone, and dichloromethane due to its hydrophobic characteristics.
  • Induction Effect: The presence of the chlorine atom, which is electronegative, may enhance interactions with polar solvents, but overall, it will favor nonpolar solvents.
  • Temperature Dependence: As with many organic compounds, solubility may increase with temperature. Warming the solvent can often help dissolve (4-chlorophenyl)-phenyl-diazene more effectively.

However, the exact solubility values can vary and are best determined experimentally. It’s important to note that while some related compounds have documented solubility, the specific behavior of (4-chlorophenyl)-phenyl-diazene remains an area open for investigation. As always, understanding the solubility of a compound is critical for applications in synthesis and chemical analysis.

Interesting facts

Interesting Facts about (4-Chlorophenyl)-Phenyl-Diazene

(4-Chlorophenyl)-phenyl-diazene, also known as a type of azo compound, exhibits a fascinating chemistry that intertwines with several fields such as organic synthesis, medicinal chemistry, and dyes. Azo compounds are characterized by the presence of the -N=N- group, which connects two aromatic groups and creates a unique resonance system.

Key Characteristics

  • Versatile Applications: This compound is often utilized in the synthesis of various dyes and pigments, thanks to its vibrant color properties.
  • Biological Relevance: Some azo compounds, including derivatives like this one, have been studied for their potential pharmacological activities, which can lead to new drug discoveries.
  • Stability and Reactivity: The stability of azo compounds can vary widely depending on the substituents present. For (4-chlorophenyl)-phenyl-diazene, the chlorophenyl group can influence its electronic properties and reactivity.
  • Historical Significance: Azo compounds have a rich history in dye chemistry, with their discovery dating back to the 19th century. They played a crucial role in the textile industry and significantly influenced organic chemistry development.

Fun Fact

One of the fascinating aspects of azo compounds like (4-Chlorophenyl)-phenyl-diazene is their ability to undergo photochemical reactions. Upon exposure to light, certain azo compounds can undergo cis-trans isomerization, altering their structure and properties. This photochemical behavior makes them interesting candidates for research in materials science and photonics.

As you explore the world of (4-Chlorophenyl)-phenyl-diazene, remember that compounds like these are not just chemical formulas; they represent vast avenues of research and potential application!

Synonyms
p-Chloroazobenzene
4340-77-6
4-CHLOROAZOBENZENE
Azobenzene, 4-chloro-
(Z)-4-Chloroazobenzene
Diazene, (4-chlorophenyl)phenyl-
Azobenzene, 4-chloro-, (E)-
Diazene, (4-chlorophenyl)phenyl-, (E)-
1-(4-chlorophenyl)-2-phenyldiazene
C12H9ClN2
6141-95-3
6530-97-8
(4-chlorophenyl)-phenyldiazene
Diazene, (4-chlorophenyl)phenyl-, (Z)-
Azobenzene, 4-chloro-, (Z)-
NSC16040
NSC 16040
p-Chloro-cis-azobenzene
p-Chloro-trans-azobenzene
SCHEMBL3283243
DTXSID90871069
NJFDMENHTAYHMA-CCEZHUSRSA-N
NJFDMENHTAYHMA-PFONDFGASA-N
NSC-16040
AKOS015997075
(E)-1-(4-Chlorophenyl)-2-phenyldiazene
(E)-1-(4-Chlorophenyl)-2-phenyldiazene #
(Z)-1-(4-Chlorophenyl)-2-phenyldiazene #