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N-(8-aminooctyl)-5-iodo-naphthalene-1-sulfonamide

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Identification
Molecular formula
C18H23IN2O2S
CAS number
93620-07-6
IUPAC name
N-(8-aminooctyl)-5-iodo-naphthalene-1-sulfonamide
State
State

At room temperature, N-(8-aminooctyl)-5-iodo-naphthalene-1-sulfonamide exists in a solid state. It is not a volatile compound under normal conditions, making it suitable for handling and use in laboratory applications related to biochemical and molecular research.

Melting point (Celsius)
185.00
Melting point (Kelvin)
458.15
Boiling point (Celsius)
383.50
Boiling point (Kelvin)
656.65
General information
Molecular weight
559.35g/mol
Molar mass
559.3500g/mol
Density
1.5600g/cm3
Appearence

N-(8-aminooctyl)-5-iodo-naphthalene-1-sulfonamide generally appears as a solid under standard conditions. The compound is often characterized by its crystalline form, which may vary in color depending on its purity and specific form. As a synthetic organic compound, it is typically used in research settings, hence its appearance is often described in terms of its crystalline or powdered state.

Comment on solubility

Solubility of N-(8-aminooctyl)-5-iodo-naphthalene-1-sulfonamide

The solubility of N-(8-aminooctyl)-5-iodo-naphthalene-1-sulfonamide (C18H23IN2O2S) can be influenced by several factors, including its chemical structure and the presence of specific functional groups. Here are some key points to consider regarding its solubility:

  • Polarity: The molecule contains both hydrophobic (naphthalene ring and octyl chain) and hydrophilic (sulfonamide group and amino group) characteristics. This dual nature often results in moderate to low water solubility.
  • Solvent Interaction: The solubility may vary significantly depending on the solvent used. For instance, it could show better solubility in organic solvents like dichloromethane or ethanol, which can help to dissolve the hydrophobic parts of the molecule.
  • Temperature Effects: Generally, higher temperatures can enhance solubility. Therefore, testing the solubility at different temperatures could yield varied results.
  • Potential Applications: Understanding the solubility is fundamental for practical applications, especially in drug formulation where solubility impacts bioavailability.

In summary, the solubility of N-(8-aminooctyl)-5-iodo-naphthalene-1-sulfonamide is a complex interplay of its structural features, solvent characteristics, and environmental conditions. Investigating these factors can provide valuable insights for its applications in various fields.

Interesting facts

Interesting Facts About N-(8-aminooctyl)-5-iodo-naphthalene-1-sulfonamide

N-(8-aminooctyl)-5-iodo-naphthalene-1-sulfonamide, also known as a sulfonamide compound, is a fascinating molecule with diverse applications in the field of medicinal chemistry and biotechnology. Here are some interesting insights:

  • Structure and Function: This compound features a naphthalene ring system, which is significant in the development of pharmaceuticals and dyes. The presence of an iodine atom adds to its *biological relevance* as halogenated compounds often exhibit unique reactivity and interactions with biological targets.
  • Biological Activity: Sulfonamides have been widely studied for their antibacterial properties. This compound's unique side chain may enhance its ability to interact with certain biological pathways or molecules, making it a candidate for developing novel therapies.
  • Application in Imaging: The iodo substituent can also be utilized for imaging applications, such as in *radiodiagnostics*. Compounds with iodine are often used in medical imaging due to iodine's effective absorption of X-rays.
  • Receptor Interaction: The presence of the amine group allows for potential interactions with various receptors in the body, which could lead to the development of compounds aimed at targeting specific diseases or conditions.
  • Research Implications: Scientists continue to explore *N-(8-aminooctyl)-5-iodo-naphthalene-1-sulfonamide* and similar compounds for their potential in developing targeted drug delivery systems, cancer therapies, and innovative imaging techniques.

In summary, N-(8-aminooctyl)-5-iodo-naphthalene-1-sulfonamide stands out not only for its complex structure but also for its promising applications in medicinal chemistry and diagnostics. The interplay of its *chemical architecture* and biological capabilities makes it an intriguing subject for research, paving the way for future advances in healthcare.

Synonyms
N-(8-Aminooctyl)-5-iodonaphthalene-1-sulfonamide
103771-14-8
N-(8-Aminooctyl)-5-Iodo-1-Naphthalenesulfonamide
DTXSID20146050
1-NAPHTHALENESULFONAMIDE, N-(8-AMINOOCTYL)-5-IODO-
DTXCID8068541
SCHEMBL17565626