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Identification

Molecular formula
C11H8O2
CAS Number
58-27-5
IUPAC Name
2-(tert-butylamino)naphthalene-1,4-dione
Molecular Weight
172.18g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2560g/cm3
Synonyms
23434-49-3
Interesting facts

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

2-(tert-butylamino)naphthalene-1,4-dione, commonly referred to as a naphthoquinone derivative, is an intriguing compound that garners interest in various fields of chemistry, particularly in organic synthesis and medicinal chemistry. Here are some noteworthy aspects of this compound:

  • Structural Significance: The presence of the tert-butylamino group enhances the lipophilicity of the compound, which can influence its biological activity and interaction with lipid membranes.
  • Reactivity: Naphthoquinones are known for their reactivity due to the presence of conjugated double bonds. This makes them valuable in organic syntheses as intermediates in the production of more complex molecules.
  • Biological Activities: Compounds like 2-(tert-butylamino)naphthalene-1,4-dione have been studied for their potential therapeutic properties, including antibacterial and anticancer activities, which could pave the way for new drug developments.
  • Application in Dyes: Similar naphthalene derivatives are frequently utilized in the dye industry due to their vivid colors and stability, showcasing their importance beyond medicinal chemistry.
  • Analytical Uses: Given its unique structure and properties, this compound can be employed as a reagent in analytical chemistry, particularly in qualitative and quantitative analysis of various substrates.

In the words of renowned chemists, “Understanding the structure-activity relationship is crucial for the development of effective pharmaceuticals.”

As the study of compounds like 2-(tert-butylamino)naphthalene-1,4-dione continues, researchers are constantly unveiling new applications and significance, making the exploration of chemical compounds a vibrant and ever-evolving field.

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