(3-methyl-4-oxido-1-oxo-quinoxalin-1-ium-2-yl)methanol

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Identification

Molecular formula
C11H10N2O3
CAS Number
123456-78-9
IUPAC Name
(3-methyl-4-oxido-1-oxo-quinoxalin-1-ium-2-yl)methanol
Molecular Weight
205.22g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2500g/cm3
Synonyms
MEQUIDOX
Interesting facts

Interesting Facts about (3-methyl-4-oxido-1-oxo-quinoxalin-1-ium-2-yl)methanol

(3-methyl-4-oxido-1-oxo-quinoxalin-1-ium-2-yl)methanol is a fascinating compound known for its unique structure and potential applications.

1. Structure and Functionality

This compound features a quinoxaline ring, which is a bicyclic structure composed of two fused aromatic rings. The presence of the oxido and oxo functional groups enhances its reactivity and potential interaction with various biological systems. Notably:

  • The methyl group contributes to the compound's overall stability and influences its reactivity.
  • The methanol group can participate in hydrogen bonding, making this compound an interesting candidate for further study in medicinal chemistry.

2. Potential Biological Activity

Quinoxaline derivatives are widely researched in the field of pharmaceutical chemistry due to their promising biological activities. Some interesting points include:

  • They have been studied for their potential anti-inflammatory properties.
  • Some derivatives are recognized for their antimicrobial, antitumor, and neuroprotective effects.

This particular compound may hold similar promise, warranting further investigation into its effects on biological systems.

3. Research Applications

In the laboratory, compounds like (3-methyl-4-oxido-1-oxo-quinoxalin-1-ium-2-yl)methanol could be utilized in:

  • Drug design, where exploring its interaction with biological targets can provide insights into new therapeutic agents.
  • Material science, where its unique properties may lead to innovations in sensor technologies or catalysis.

4. The Role of Quinoxaline in Chemistry

Quinoxaline and its derivatives serve as important building blocks in organic synthesis due to their versatility. As a chemist, it’s crucial to understand why:

  • Quinoxaline derivatives can serve as ligands in coordination chemistry.
  • Their unique electronic characteristics make them suitable for applications in organic electronics.

In summary, (3-methyl-4-oxido-1-oxo-quinoxalin-1-ium-2-yl)methanol is a compound that embodies both structural elegance and potential functionality, making it an exciting topic of study in the realms of chemistry and pharmacology.

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