2-Dimethylaminonaphthoquinone

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Identification

Molecular formula
C12H11NO2
CAS Number
73642-48-3
IUPAC Name
2-(dimethylamino)naphthalene-1,4-dione
Molecular Weight
213.24g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2500g/cm3
Synonyms
2-Dimethylamino-1, 4-naphthoquinone
Interesting facts

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

2-(dimethylamino)naphthalene-1,4-dione, often referred to as a versatile chemical compound, carries notable significance in various scientific applications. Here are some interesting aspects to consider:

  • Structural Features: This compound contains a naphthalene core with a dimethylamino group, which provides unique electronic properties that can influence its reactivity and interactions with other substances.
  • Reactive Nature: The presence of the quinone structure makes this compound particularly reactive, allowing it to participate in diverse chemical reactions, making it a valuable intermediate in organic synthesis.
  • Color and Dyes: Compounds like 2-(dimethylamino)naphthalene-1,4-dione are often studied for their potential use in dyes and pigments, especially in the textile industry, due to their vivid color properties.
  • Biological Significance: Scientists have explored this compound in the field of biochemistry, as it may have implications in studies related to enzymatic processes and electron transfer mechanisms.
  • Historical Context: Compounds in the naphthalene family have been utilized since the 19th century, making their study a foundational part of organic chemistry that continues to evolve with modern techniques.

In summary, 2-(dimethylamino)naphthalene-1,4-dione stands out not only for its structural characteristics but also for its wide-ranging applications in chemistry, biochemistry, and materials science. As scientists continue to investigate its properties and reactions, this compound remains a fascinating topic of study.

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