N-(5-aminopentyl)-5-chloro-naphthalene-2-sulfonamide
- Molecular formula
- C15H19ClN2O2S
- CAS Number
- 852227-78-2
- IUPAC Name
- N-(5-aminopentyl)-5-chloro-naphthalene-2-sulfonamide
- Molecular Weight
- 339.84g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.3500g/cm3
Identification
Interesting Facts about N-(5-Aminopentyl)-5-chloro-naphthalene-2-sulfonamide
N-(5-Aminopentyl)-5-chloro-naphthalene-2-sulfonamide is a fascinating compound that belongs to the class of sulfonamide antibiotics. Below are some intriguing aspects of this compound:
- Applications in Medicine: This compound is significant in medicinal chemistry, often investigated for its potential antimicrobial properties. The presence of the sulfonamide group is known to inhibit bacterial growth, making it a target for drug development.
- Genetic Studies: The compound is sometimes utilized in genetic research, particularly concerning the interactions of small molecules with enzymatic pathways. Researchers are keen to explore its role in gene regulation and expression.
- Unique Structure: The structure of this compound features a naphthalene moiety, which contributes to its hydrophobic nature, enhancing its interaction with biological membranes.
- Chloro Group Influence: The chlorine atom in the structure can significantly affect the compound's reactivity and biological activity, often allowing for diverse interactions within biological systems.
As one delves deeper into the study of N-(5-aminopentyl)-5-chloro-naphthalene-2-sulfonamide, it becomes apparent that understanding its properties not only contributes to the fields of biochemistry and pharmacology but also opens pathways for innovative therapies. Scientists often say, "The design of new molecules can lead to breakthroughs in our understanding of life itself."
Overall, the study of such compounds enriches the chemical sciences and inspires new directions in research.