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(4-aminophenyl)sulfonyl-quinoxalin-2-yl-azanide

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Identification
Molecular formula
C14H12N4O2S
CAS number
:null
IUPAC name
(4-aminophenyl)sulfonyl-quinoxalin-2-yl-azanide
State
State

The compound is a solid at room temperature, which is typically 20-25°C. Its crystalline nature allows it to be handled as a powder or small granules in laboratory and industrial settings.

Melting point (Celsius)
180.00
Melting point (Kelvin)
453.15
Boiling point (Celsius)
300.00
Boiling point (Kelvin)
573.15
General information
Molecular weight
324.36g/mol
Molar mass
324.3640g/mol
Density
1.4000g/cm3
Appearence

The compound typically appears as a crystalline solid, with a distinct shape based on its molecular structure. The exact color and texture depend on the purity and specific formation process of the compound sample. It may exhibit a powdery or granular texture suitable for certain experimental or industrial applications.

Comment on solubility

Solubility of (4-aminophenyl)sulfonyl-quinoxalin-2-yl-azanide

The solubility of (4-aminophenyl)sulfonyl-quinoxalin-2-yl-azanide (C14H12N4O2S) is a property influenced by various factors, including its chemical structure and temperature. This compound exhibits a moderate level of solubility in different solvents, which can be summarized as follows:

  • Organic Solvents: It tends to dissolve readily in polar organic solvents such as dimethyl sulfoxide (DMSO) and methanol.
  • Aqueous Solubility: The solubility in water is limited, primarily due to the hydrophobic portions of the molecule, although slight solubility may be observed under certain pH conditions.
  • Temperature Dependence: Increasing the temperature generally enhances solubility for many compounds, and this one may also show an increased solubility profile at higher temperatures.

When analyzing solubility, it's crucial to note that intermolecular interactions play a significant role. The presence of functional groups, such as the amine and sulfonyl groups, can interact favorably with solvent molecules, aiding in solvation. Thus, the solubility of this compound can be characterized as:

  • Moderate in polar solvents
  • Low in non-polar solvents

In conclusion, understanding the solubility behavior of (4-aminophenyl)sulfonyl-quinoxalin-2-yl-azanide is essential for its practical applications in pharmaceuticals and chemical research, as it influences both the bioavailability and the effectiveness of the compound in various chemical environments.

Interesting facts

Discovering (4-aminophenyl)sulfonyl-quinoxalin-2-yl-azanide

(4-aminophenyl)sulfonyl-quinoxalin-2-yl-azanide is a fascinating compound that has caught the attention of researchers due to its unique chemical structure and potential applications. Here are some intriguing aspects of this compound:

  • Versatile Structure: The presence of both a sulfonamide group and a quinoxaline moiety in its structure allows this compound to exhibit a variety of chemical behaviors, which can be beneficial for medicinal chemistry.
  • Biological Activity: Quinoxaline derivatives, including this compound, are known for their biological activities, particularly as potential agents in therapeutic applications for diseases such as cancer, diabetes, and inflammation.
  • Research Potential: Studies have suggested that compounds with similar backbones may serve as important scaffolds for the development of novel pharmaceuticals, emphasizing the importance of (4-aminophenyl)sulfonyl-quinoxalin-2-yl-azanide in ongoing research.
  • Synthetic Pathways: The synthesis of this compound involves several steps that typically include the formation of the sulfonamide and quinoxaline components, showcasing the complexity and skill involved in organic synthesis.

As chemists delve deeper into the properties and potential uses of (4-aminophenyl)sulfonyl-quinoxalin-2-yl-azanide, they are not only uncovering the intricacies of its behavior in chemical reactions but also its promise in the field of medicine. By studying such compounds, scientists continue to expand their understanding of chemical interactions and the potential for innovation in drug discovery.

In the words of a noted chemist, "Chemistry is the art of turning the mundane into the extraordinary through the lens of the molecular world." This compound embodies that ethos, inviting further exploration and appreciation.

Synonyms
NSC683543
4-amino-N-quinoxalin-2-yl-benzenesulfonamide
NCGC00178376-01
NCGC00178376-02
SBI-0051657.P002
AB00053606
AB00053606_08
Benzenesulfonamide, 4-amino-N-2-quinoxalinyl-, ion(1-)