4-(2-amino-1-phenylethyl)aniline

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Identification

Molecular formula
C14H16N2
CAS Number
1234-65-7
IUPAC Name
4-(2-amino-1-phenyl-ethyl)aniline
Molecular Weight
198.30g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1070g/cm3
Synonyms
Skf 12185
Interesting facts

Exploring 4-(2-amino-1-phenyl-ethyl)aniline

4-(2-amino-1-phenyl-ethyl)aniline, often abbreviated as 4-AEP, is a fascinating compound with a rich background in organic chemistry. Here are some interesting facts that highlight its significance:

  • Synthetic Versatility: 4-AEP is widely used in the synthesis of various organic compounds and serves as a crucial intermediate in the production of dyes and pigments.
  • Biological Relevance: The compound's structure, featuring an amino group, suggests potential biological activity, making it a candidate for pharmacological studies.
  • Color Chemistry: Due to its aniline base, 4-AEP can participate in diazotization reactions, leading to the formation of vibrant azo compounds, which are essential in textile and ink industries.
  • Research Potential: Scientists are exploring the compound's application in materials science, particularly in the development of organic semiconductors and electronic devices.
  • Foundation in Aromatic Chemistry: As an aromatic amine, 4-AEP exemplifies the properties of aromatic compounds, such as stability and reactivity, making it a subject of study for those interested in organic reactions.

In summary, 4-(2-amino-1-phenyl-ethyl)aniline is not just a simple organic compound; it plays a pivotal role in various fields ranging from dye synthesis to potential medicinal applications. Its multifaceted nature continues to intrigue chemists and researchers alike.

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