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Moxalactam

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Identification
Molecular formula
C20H20N4O6S
CAS number
61147-90-6
IUPAC name
(2S)-3-methyl-2-(quinoxaline-2-carbonylamino)pentanoic acid
State
State

At room temperature, moxalactam is typically a solid. It is stable under normal conditions and can be found in various pharmaceutical formulations as a powder or in solution.

Melting point (Celsius)
205.00
Melting point (Kelvin)
478.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
456.46g/mol
Molar mass
458.0000g/mol
Density
1.3600g/cm3
Appearence

Moxalactam appears as an off-white to light yellow crystalline powder. Its appearance can vary slightly depending on its form and purity.

Comment on solubility

Solubility of (2S)-3-methyl-2-(quinoxaline-2-carbonylamino)pentanoic acid

The solubility characteristics of (2S)-3-methyl-2-(quinoxaline-2-carbonylamino)pentanoic acid can vary based on different factors, such as temperature and pH. Generally speaking, the solubility of this compound is influenced by the following key factors:

  • Polarity: The presence of polar functional groups in the molecule can enhance solubility in polar solvents, such as water. Quinoxaline and carboxyl groups are polar, suggesting that this compound may exhibit moderate aqueous solubility.
  • pH Level: Changes in pH can significantly impact the ionization state of carboxylic acids. At lower pH, the compound may exist in its protonated form, whereas at higher pH levels, deprotonation can lead to increased solubility.
  • Temperature: Solubility often increases with rising temperature, which can promote the dissolution of solids in solvents.
  • Concentration of Solvent: The solvent's own concentration and the presence of other solutes can either enhance or inhibit the solubility of this compound.

In conclusion, while specific solubility data for (2S)-3-methyl-2-(quinoxaline-2-carbonylamino)pentanoic acid might be limited, understanding the interactions of its functional groups can provide valuable insights into its potential for dissolution in various environments. As noted, the complex interplay of these factors makes predicting solubility a nuanced endeavor.

Interesting facts

Interesting Facts about (2S)-3-methyl-2-(quinoxaline-2-carbonylamino)pentanoic acid

(2S)-3-methyl-2-(quinoxaline-2-carbonylamino)pentanoic acid, a compelling compound in the realm of medicinal chemistry, showcases a unique molecular structure that links amino acids with bioactive heterocycles. Here are some intriguing aspects of this compound:

  • Biological Significance: This compound has garnered attention for its potential therapeutic applications, particularly in the field of neurology and cancer research due to its structural resemblance to certain neurotransmitters and pharmacologically active molecules.
  • Heterocyclic Chemistry: The incorporation of a quinoxaline moiety adds an intriguing layer, as quinoxalines are known for their diverse biological properties, including anti-inflammatory and antitumor activities.
  • Chirality in Chemistry: The presence of the (2S) configuration emphasizes the importance of stereochemistry in drug design. The specific stereoisomer can lead to significant differences in biological activity, making this aspect of the molecule critical for its function.
  • Potential Pathways: This compound may influence various biochemical pathways related to the metabolism of amino acids and neurochemical processes, hinting at its role in complex physiological systems.
  • Research Opportunities: As scientists continue to investigate its properties, (2S)-3-methyl-2-(quinoxaline-2-carbonylamino)pentanoic acid stands as a promising candidate for further study in both synthetic and medicinal chemistry.

The exploration of (2S)-3-methyl-2-(quinoxaline-2-carbonylamino)pentanoic acid not only contributes valuable insights to organic synthesis but also enhances our understanding of complex biochemical interactions and their implications in health and disease. As noted by one researcher, "Understanding the intricate relationships between structure and function remains a cornerstone of medicinal chemistry."

Synonyms
N-(2-Quinoxaloyl)-L-isoleucine
NSC 96557
BRN 0678743
ISOLEUCINE, N-(2-QUINOXALOYL)-, L-
Isoleucine, N-(2-quinoxalinylcarbonyl)-, L-
Isoleucine, N-(2-quinoxalinylcarbonyl)-, L-(8CI)
AKOS010419026