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(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
State
State

At room temperature, this compound is found in solid form. It is relatively stable under ambient conditions, though care should be taken to minimize exposure to moisture and light, which can lead to degradation.

Melting point (Celsius)
189.00
Melting point (Kelvin)
462.00
Boiling point (Celsius)
380.00
Boiling point (Kelvin)
653.00
General information
Molecular weight
205.22g/mol
Molar mass
205.2150g/mol
Density
1.2500g/cm3
Appearence

The compound is typically found as a crystalline solid with a pale yellow coloration. It can also be slightly hygroscopic, tending to absorb moisture from the air, leading to clumping if not stored properly.

Comment on solubility

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

The solubility of (3-methyl-4-oxido-1-oxo-quinoxalin-1-ium-2-yl)methanol can be influenced by various factors. Being a quinoxaline derivative, this compound exhibits unique characteristics concerning its solubility:

  • Polarity: The presence of the quaternary ammonium functional group typically contributes to increased solubility in polar solvents such as water, but can also lead to limited solubility in non-polar solvents.
  • Hydrogen Bonding: The hydroxyl group in the methanol component can form hydrogen bonds with water molecules, enhancing solubility further. This allows it to dissolve well in polar solvents.
  • Cationic Nature: Its ionic structure enables it to interact readily with anionic species, which may influence its solubility in various solutions.
  • Temperature Effects: As with many chemical compounds, solubility can increase with temperature due to enhanced molecular activity.

It’s essential to note that while (3-methyl-4-oxido-1-oxo-quinoxalin-1-ium-2-yl)methanol is likely to be soluble in polar solvents, the degree of solubility may vary based on concentration, pH, and the presence of other ionic species in the solution.
In summary, factors such as polarity, hydrogen bonding capabilities, and ionic interactions greatly dictate the solubility profile of this compound, making it necessary to investigate these aspects thoroughly for practical applications.

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.

Synonyms
MEQUIDOX
16915-79-0
GS-7443
2-Quinoxalinemethanol, 3-methyl-, 1,4-dioxide
3-Methyl-2-quinoxalinemethanol 1,4-dioxide
NSC-352521
GS 7443
MEQUIDOX [USAN]
MEQUIDOX [INN]
DTXSID30168667
4UV6363I81
Mequidox [USAN:INN]
mequidoxum
UNII-4UV6363I81
NSC 352521
3-Methyl-2-chinoxalinmethanol 1,4-dioxid
DTXCID4091158
2-(Hydroxymethyl)-3-methylquinoxaline 1,4-dioxide
(3-methyl-4-oxido-1-oxoquinoxalin-1-ium-2-yl)methanol
NSC352521
3-Methyl-2-quinoxalinylmethanol N(sup1),N(sup4)-dioxide
2-(HYDROXYMETHYL)-3-METHYLQUINOXALINE-1,4-DIIUM-1,4-BIS(OLATE)
SCHEMBL193980
CHEMBL2105178
MZRHTYDFTZJMLV-UHFFFAOYSA-N
2-Quinoxalinemethanol, 1,4-dioxide
AKOS015901623
AKOS016013793
CS-0447818
NS00123656
2-hyroxymethyl-3-methylquinoxaline-1,4-dioxide
2-hydroxymethyl-3-methylquinoxaline-1,4-dioxide
2-(Hydroxymethyl)-3-methylquinoxaline1,4-dioxide
2-(Hydroxymethyl)-3-methylquinoxaline N,N'-dioxide
2-(Hydroxymethyl)-3-methylquinoxaline N, N'-dioxide
Q27260533
(3-methyl-1,4-dioxido-quinoxaline-1,4-diium-2-yl)methanol
2-(Hydroxymethyl)-3-methyl-1-oxoquinoxalin-1-ium-4(1H)-olate
MEQUINDOX [2-ACETYL-3-METHYLQUINOXALINEDIUM-1,4-DIOLATE]
2-(Hydroxymethyl)-3-methyl-1.lambda.~5~,4.lambda.~5~-quinoxaline-1,4-diol