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Identification

Molecular formula
C11H8O2
CAS Number
58-27-5
IUPAC Name
2-(cyclohexylmethylamino)naphthalene-1,4-dione
Molecular Weight
172.19g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3350g/cm3
Synonyms
1, 4-NAPHTHOQUINONE, 2-(CYCLOHEXYLMETHYLAMINO)-
Interesting facts

Interesting Facts about 2-(cyclohexylmethylamino)naphthalene-1,4-dione

The compound 2-(cyclohexylmethylamino)naphthalene-1,4-dione, often regarded in the realm of organic chemistry for its unique structure and potential applications, presents a fascinating study in both synthesis and reactivity. Here are some key insights:

  • Structural Significance: This compound features a naphthalene ring system, which is well-known for its stability and optical properties. The presence of a cyclohexylmethylamino group greatly influences its chemical behavior, offering interesting opportunities for interactions with biological molecules.

  • Biological Activity: Compounds like this one have been noted for their biological activities, particularly in medicinal chemistry. They may exhibit properties such as anti-cancer, anti-inflammatory, or anti-oxidant actions, which makes them attractive candidates for further research in drug development.

  • Versatile Synthesis: The synthesis of derivatives of naphthalene-1,4-dione typically employs a variety of organic reactions. This compound can serve as a precursor for further synthetic modifications, leading to a library of functional compounds with varied applications.

  • Research Applications: As a subject of ongoing research, 2-(cyclohexylmethylamino)naphthalene-1,4-dione is explored for its potential uses in organic electronics, dyes, and sensors. The modified naphthalene derivatives often show promising electronic properties that are useful in the development of new materials.

  • Experimental Techniques: Studying this compound involves advanced techniques such as NMR spectroscopy, mass spectrometry, and X-ray crystallography for structural determination and analysis of its properties.

In conclusion, 2-(cyclohexylmethylamino)naphthalene-1,4-dione is not just an ordinary compound; it stands as a bridge between traditional organic chemistry and innovative applications in various scientific fields, highlighting the importance of exploring such intricate molecular structures.

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