N-(2-hydroxyethyl)-N-(2-hydroxypropyl)-4-methyl-benzenesulfonamide

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Identification

Molecular formula
C13H21NO4S
CAS Number
64265-45-8
IUPAC Name
N-(2-hydroxyethyl)-N-(2-hydroxypropyl)-4-methyl-benzenesulfonamide
Molecular Weight
273.35g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.1720g/cm3
Appearance
can vary slightly depending on the specific crystalline form and the level of impurities present.
Synonyms
26831-90-3
Interesting facts

Interesting Facts about N-(2-hydroxyethyl)-N-(2-hydroxypropyl)-4-methyl-benzenesulfonamide

N-(2-hydroxyethyl)-N-(2-hydroxypropyl)-4-methyl-benzenesulfonamide, often abbreviated as HEMPS, is a fascinating compound in the realm of medicinal chemistry. This compound is noteworthy for a number of reasons:

  • Dual Hydroxy Groups: The presence of two hydroxy groups in its structure not only enhances the solubility of HEMPS in biological systems but also contributes to its ability to form hydrogen bonds, which is vital for its interaction with biological targets.
  • Functional Versatility: HEMPS is classified as a sulfonamide. Sulfonamides are known for their diverse pharmacological activities, including antibacterial, diuretic, and carbonic anhydrase inhibitory effects, making compounds like HEMPS attractive in drug development.
  • Therapeutic Potential: The unique combination of the benzene sulfonamide group with hydroxyethyl and hydroxypropyl moieties could grant HEMPS potential applications in treating various health conditions. Research has indicated that such compounds may be effective as anti-inflammatory agents.
  • Structural Insights: The use of substituted benzene rings in medicinal compounds is common, and HEMPS exemplifies the trend of incorporating alkyl groups, like the 4-methyl, to fine-tune the biological activity and improve safety profiles.
  • Research and Development: Ongoing research into sulfonamide derivatives suggests that modifications to their structure can result in improved biological activity and reduced side effects, making HEMPS a candidate for further exploration in pharmaceutical applications.

As we explore the potential of N-(2-hydroxyethyl)-N-(2-hydroxypropyl)-4-methyl-benzenesulfonamide, it not only emphasizes the importance of structural modifications in medicinal chemistry but also inspires continued innovation in the aesthetic and practical applications of organic compounds.

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