N-(2-aminoethyl)-5-chloro-naphthalene-1-sulfonamide

ADVERTISEMENT

Identification

Molecular formula
C12H13ClN2O2S
CAS Number
73240-63-0
IUPAC Name
N-(2-aminoethyl)-5-chloro-naphthalene-1-sulfonamide
Molecular Weight
318.78g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.4000g/cm3
Synonyms
N-(2-Aminoethyl)-5-chloronaphthalene-1-sulfonamide
Interesting facts

Interesting Facts about N-(2-Aminoethyl)-5-chloro-naphthalene-1-sulfonamide

N-(2-aminoethyl)-5-chloro-naphthalene-1-sulfonamide, commonly referred to in scientific literature as an important organic compound, has several intriguing attributes worth noting:

  • Pharmaceutical Relevance: This compound is often studied for its potential application as a pharmaceutical agent. It belongs to a class of sulfonamides, compounds known for their effectiveness as antibiotics and antibacterial agents.
  • Structure and Function: The unique naphthalene ring within the compound provides significant aromatic stability, which can enhance its biologically relevant properties.
  • Chlorine Substitution: The presence of chlorine in the molecular structure contributes to the compound's reactivity and can influence its biological activity, making it a subject of investigation in drug design.
  • Research Focus: Ongoing research often explores how modifications of the aminoethyl and sulfonamide groups affect the compound's pharmacological profile, potentially leading to novel therapeutic agents.
  • Historical Context: Sulfonamides made their mark in history as some of the first synthetic antibiotics. N-(2-aminoethyl)-5-chloro-naphthalene-1-sulfonamide continues this legacy, showing promise in modern medicinal chemistry.

In summary, N-(2-aminoethyl)-5-chloro-naphthalene-1-sulfonamide is a fascinating substance that bridges historical significance with contemporary scientific inquiry. Its complex structure and potential pharmacological applications make it a noteworthy topic for any chemistry enthusiast or professional.

ADVERTISEMENT