2-amino-3-chloro-1,4-naphthoquinone

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Identification

Molecular formula
C10H6ClNO2
CAS Number
1198-06-1
IUPAC Name
2-amino-3-chloro-naphthalene-1,4-dione
Molecular Weight
221.61g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.5800g/cm3
Synonyms
2797-51-5
Interesting facts

Interesting Facts about 2-amino-3-chloro-naphthalene-1,4-dione

2-amino-3-chloro-naphthalene-1,4-dione is a fascinating compound that belongs to the class of naphthoquinone derivatives. Here are some captivating insights:

  • Diverse Applications: This compound is utilized in various fields such as organic synthesis, pharmaceuticals, and dyes. Its derivatives often possess valuable biological activities, making them important in medicinal chemistry.
  • Structural Significance: The presence of both amino and chloro groups in its structure contributes to its reactivity and interaction with various biological systems. The arrangement of atoms in the naphthalene ring allows for interesting electronic properties.
  • Biological Activity: Compounds like 2-amino-3-chloro-naphthalene-1,4-dione exhibit potential antimicrobial and cytotoxic activities. Research continues to explore these properties, aiming at developing new therapeutic agents.
  • Synthetic Pathways: The synthesis of this compound typically involves multi-step reactions, starting with naphthalene and incorporating chlorination and amination processes. This complexity can be both a challenge and an opportunity for chemists looking to innovate.
  • Color Chemistry: Due to the presence of naphthoquinone in its structure, this compound may participate in color-forming reactions that can be exploited in the dye industry. Its vibrant hues are appealing in various applications.

This compound not only showcases the intricate world of organic chemistry but also highlights the ongoing potential for new discoveries in therapeutic and industrial applications. As research uncovers more about its properties and functions, 2-amino-3-chloro-naphthalene-1,4-dione stands as a testament to the diversity of chemical compounds.

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