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N-(5-aminopentyl)-5-chloro-naphthalene-2-sulfonamide

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Identification
Molecular formula
C15H19ClN2O2S
CAS number
852227-78-2
IUPAC name
N-(5-aminopentyl)-5-chloro-naphthalene-2-sulfonamide
State
State

At room temperature, N-(5-aminopentyl)-5-chloro-naphthalene-2-sulfonamide exists in a solid state. It is typically stable at standard temperature and pressure, with a slight odor characteristic of organic sulfonamides.

Melting point (Celsius)
160.00
Melting point (Kelvin)
433.15
Boiling point (Celsius)
395.90
Boiling point (Kelvin)
669.05
General information
Molecular weight
339.84g/mol
Molar mass
339.8350g/mol
Density
1.3500g/cm3
Appearence

The compound N-(5-aminopentyl)-5-chloro-naphthalene-2-sulfonamide typically appears as a crystalline solid. The crystals are often white to off-white in color, and the compound may be provided as a powder for ease of handling. In its pure form, it is not hygroscopic, maintaining its solid structure under room temperature conditions.

Comment on solubility

Solubility of N-(5-aminopentyl)-5-chloro-naphthalene-2-sulfonamide (C15H19ClN2O2S)

The solubility of chemical compounds can significantly affect their practical applications, including pharmaceuticals and chemical synthesis. For N-(5-aminopentyl)-5-chloro-naphthalene-2-sulfonamide, several factors contribute to its solubility profile:

  • Polarity: The presence of functional groups such as sulfonamide and amino groups suggests that this compound may have some degree of polarity.
  • Hydrogen Bonding: The amino and sulfonamide groups could enable hydrogen bonding with solvent molecules, which generally increases solubility in polar solvents like water.
  • Hydrophobic Interactions: The naphthalene ring structure is largely hydrophobic, which might limit solubility in highly polar solvents.

In general terms:

  • Such compounds are often sparingly soluble in water.
  • They might show higher solubility in organic solvents such as ethanol or dichloromethane.

In conclusion, while specific solubility data for N-(5-aminopentyl)-5-chloro-naphthalene-2-sulfonamide may not be readily available, understanding the chemical structure and functional groups offers valuable insights into its expected solubility behavior.

Interesting facts

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.