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o-Tolyl(phenyl)diazene

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Identification
Molecular formula
C13H12N2
CAS number
119-24-4
IUPAC name
o-tolyl(phenyl)diazene
State
State
At room temperature, o-Tolyl(phenyl)diazene is usually encountered as a liquid.
Melting point (Celsius)
20.00
Melting point (Kelvin)
293.15
Boiling point (Celsius)
341.00
Boiling point (Kelvin)
614.15
General information
Molecular weight
196.25g/mol
Molar mass
197.2520g/mol
Density
1.0700g/cm3
Appearence

o-Tolyl(phenyl)diazene is typically a reddish-yellow liquid. It is known for its intense color and is often used in chemical research for creating azo compounds.

Comment on solubility

Solubility of o-Tolyl(phenyl)diazene

The solubility characteristics of o-tolyl(phenyl)diazene are fascinating and can significantly influence its applications in various fields. This compound, with the chemical formula C13H12N2, demonstrates notable solubility behavior that can be attributed to its molecular structure.

In general, o-tolyl(phenyl)diazene is:

  • Slightly soluble in water: The presence of the diazene functional group can lead to some intermolecular interactions with water, yet the overall hydrophobic nature of the aromatic rings limits its solubility.
  • More soluble in organic solvents: Solvents such as ethanol, acetone, and ethyl acetate typically promote better solubility due to their non-polar characteristics, which align more closely with the non-polar regions of the molecule.
  • Influenced by temperature: Like many organic compounds, the solubility of o-tolyl(phenyl)diazene tends to increase with higher temperatures, enable easier dissolution in solvents.

As noted, "the solubility of a compound is often a key factor in determining its utility in various applications." Therefore, understanding the solubility properties of o-tolyl(phenyl)diazene is critical for researchers and practitioners working with this compound in laboratory or industrial settings.

Interesting facts

Exploring o-Tolyl(phenyl)diazene

o-Tolyl(phenyl)diazene is a fascinating compound in the world of organic chemistry, known for its intriguing properties and applications. Here are some key facts that every chemistry enthusiast should know:

  • Diazene Structure: This compound features a diazene functional group, characterized by a nitrogen-nitrogen double bond. The diazene moiety is notable for its reactivity, particularly under appropriate conditions.
  • Substituents Matter: The presence of o-tolyl (an ortho-substituted methyl group on the phenyl ring) adds unique steric and electronic effects, influencing the compound's reactivity and stability. This makes it a subject of interest in studies of aromatic substitutions.
  • Applications: o-Tolyl(phenyl)diazene is employed in various fields, including polymers and dyes. Its ability to serve as a precursor or intermediate in synthesizing more complex organic molecules showcases its versatility.
  • Reactivity: The compound can undergo reactions such as azo-coupling, which allows it to form larger oligomers or polymers. These reactions are widely utilized in the dye industry to develop vibrant colors.

In summary, o-Tolyl(phenyl)diazene stands out for its unique structural characteristics and diverse applications, making it a remarkable molecule to study. \"Understanding the role of diazenes in organic synthesis opens the door to novel materials and complex compounds.\" This quote encapsulates the spirit of innovation brought forth by compounds like o-tolyl(phenyl)diazene.

Synonyms
6676-90-0
(2-METHYLPHENYL)PHENYLDIAZENE
o-methylazobenzol
NSC243783
SCHEMBL2997137
SCHEMBL11695762
CFNRNHFKQPOFMH-CCEZHUSRSA-N
CFNRNHFKQPOFMH-UHFFFAOYSA-N
Diazene, (2-methylphenyl)phenyl-
(E)-(2-methylphenyl)-phenyldiazene
NSC 243783
NSC-243783
(E)-1-(2-Methylphenyl)-2-phenyldiazene #