Skip to main content

Sulfathiazole and Phenylephrine

ADVERTISEMENT
Identification
Molecular formula
C9H9N3O2S2; C9H13NO2
CAS number
721-30-6; 59-42-7
IUPAC name
4-amino-N-thiazol-2-yl-benzenesulfonamide;3-[1-hydroxy-2-(methylamino)ethyl]phenol
State
State

At room temperature, both Sulfathiazole and Phenylephrine exist as solids. They are each available in crystalline form.

Melting point (Celsius)
202.00
Melting point (Kelvin)
475.15
Boiling point (Celsius)
316.27
Boiling point (Kelvin)
589.42
General information
Molecular weight
270.33g/mol
Molar mass
270.3320g/mol
Density
1.4860g/cm3
Appearence

Sulfathiazole appears as an off-white crystalline powder, while Phenylephrine is typically found as a white to slightly yellow crystalline powder. Both have distinct crystalline structures typical of many small organic molecules.

Comment on solubility

Solubility of 4-amino-N-thiazol-2-yl-benzenesulfonamide; 3-[1-hydroxy-2-(methylamino)ethyl]phenol

This compound exhibits unique solubility characteristics worth discussing. Solubility is a critical property that determines how a substance interacts within various environments, particularly in biological systems and industrial applications. Here are some key points regarding its solubility:

  • Solvent Dependence: The solubility of this compound can vary significantly with different solvents, often showing higher solubility in polar solvents due to the presence of hydrophilic functional groups.
  • Influence of pH: The solubility may also be influenced by the pH of the solution. At different pH levels, ionization of the amine and sulfonamide groups can occur, enhancing or decreasing solubility.
  • Temperature Effects: Generally, increasing temperature tends to increase the solubility of solid substances in liquids, although exceptions apply depending on the specific interactions present in this compound.

In summary, it's essential to consider various factors such as solvent choice, pH, and temperature when assessing the solubility of 4-amino-N-thiazol-2-yl-benzenesulfonamide; 3-[1-hydroxy-2-(methylamino)ethyl]phenol. As underscored by the dynamic nature of solubility, “the conditions surrounding a compound can significantly influence its form and function.” Understanding this can aid in optimizing its application in diversified fields.

Interesting facts

Interesting Facts about 4-amino-N-thiazol-2-yl-benzenesulfonamide; 3-[1-hydroxy-2-(methylamino)ethyl]phenol

The compound 4-amino-N-thiazol-2-yl-benzenesulfonamide; 3-[1-hydroxy-2-(methylamino)ethyl]phenol presents a fascinating intersection of medicinal chemistry and organic synthesis. It is notable for several reasons:

  • Dual Functionality: This compound incorporates both a thiazole ring and a phenolic group, which may contribute to enhanced biological activity and the potential for diverse pharmacological applications.
  • Antimicrobial Properties: Many compounds in the sulfonamide class, including this one, are known for their antibacterial properties. This makes it an important subject of study in antibiotic development.
  • Structural Diversity: The combination of the thiazole moiety and the sulfonamide structure provides unique electronic properties that can influence the compound's reactivity and interaction with biological targets.
  • Potential Therapeutic Uses: Compounds like this have shown promise in treating various diseases, including cancers and infections, underscoring the importance of novel pharmaceutical development.
  • Synthesis Challenges: The synthesis of such compounds often involves intricate multi-step reactions, which offer exciting challenges for synthetic chemists.

As summarized by a well-known chemist, “Great discoveries are often made by not being afraid to try something new”. This sentiment captures the essence of exploring complex compounds like 4-amino-N-thiazol-2-yl-benzenesulfonamide; 3-[1-hydroxy-2-(methylamino)ethyl]phenol, where the potential for innovation is coupled with the promise of significant scientific advancements.

This compound is not just a theoretical construct; it represents the convergence of chemistry and medicine, driving forward research that can have profound impacts on health and disease management.

Synonyms
AGN-PC-0JKHJX
7645-09-2
DTXSID20274766