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- Molecular formula
- C16H21ClN2O2S
- CAS Number
- 110448-33-4
- IUPAC Name
- N-(6-aminohexyl)-5-chloro-naphthalene-1-sulfonamide
- Molecular Weight
- 376.88g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.3500g/cm3
- Synonyms
- N-(6-AMINOHEXYL)-5-CHLORO-1-NAPHTHALENESULFONAMIDE
Identification
Interesting facts
Interesting Facts About N-(6-Aminohexyl)-5-chloro-naphthalene-1-sulfonamide
N-(6-Aminohexyl)-5-chloro-naphthalene-1-sulfonamide is an intriguing compound with a variety of chemical properties and potential applications. Here are some fascinating aspects of this compound:
- Pharmaceutical Relevance: This compound is part of a class of sulfonamides that have been extensively studied for their antimicrobial properties. Its structure suggests potential efficacy against various bacterial infections.
- Versatile Chemistry: The presence of both an amino group and a sulfonyl group in its structure allows for diverse chemical reactivity. This versatility can lead to significant implications in drug development.
- Structure-Activity Relationship (SAR): The specific arrangement of functional groups contributes to the compound's biological activity. Researchers often focus on SAR to modify compounds to enhance their effectiveness while reducing side effects.
- Environmental Science: This compound may be researched for its behavior in environmental contexts, particularly regarding its stability and degradation pathways, as sulfonamide antibiotics can impact ecosystems.
- Potential Industrial Applications: Beyond medicinal uses, N-(6-aminohexyl)-5-chloro-naphthalene-1-sulfonamide may find roles in the development of inhibitors in chemical processes, showcasing its multifunctional capabilities.
As a compound at the intersection of organic chemistry and pharmacology, N-(6-aminohexyl)-5-chloro-naphthalene-1-sulfonamide illustrates the complexity and potential of chemical research. Scientists continue to explore its properties, aiming to unlock further therapeutic applications and improve our understanding of sulfonamides.