4-(2-amino-1-phenylethyl)aniline
ADVERTISEMENT
- 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
Identification
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.