Skip to main content

Iodophenyltrimethylnorbornylammonium chloride hydroiodide

ADVERTISEMENT
Identification
Molecular formula
C20H28INCl
CAS number
63589-46-8
IUPAC name
(4-iodophenyl)methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride;hydroiodide
State
State

At room temperature, it exists as a crystalline solid. It is typically stable and should be handled with care to prevent exposure to moisture or air as it might degrade further, particularly the iodide component, under such conditions.

Melting point (Celsius)
180.00
Melting point (Kelvin)
453.15
Boiling point (Celsius)
350.00
Boiling point (Kelvin)
623.15
General information
Molecular weight
455.50g/mol
Molar mass
455.5000g/mol
Density
2.7000g/cm3
Appearence

The compound typically appears as a white to off-white crystalline solid. The presence of both chloride and hydroiodide salts can sometimes impart a slightly yellowish or brownish hue depending on the specific conditions of purification and crystallization.

Comment on solubility

Solubility of (4-iodophenyl)methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride;hydroiodide

The solubility of (4-iodophenyl)methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride;hydroiodide is influenced by a variety of factors due to its complex structure. Understanding its solubility can be essential for various applications in both academic research and industrial processes.

Factors Affecting Solubility:

  • Polarity: The presence of an ammonium group tends to enhance solubility in polar solvents such as water.
  • Ionic Nature: As a quaternary ammonium salt, it typically exhibits good solubility in ionic solutions, particularly in those containing chloride ions.
  • Temperature: Like many compounds, solubility often increases with temperature, allowing for better dissolution in solvents.
  • Hydrophobic Regions: The trimethyl norbornane moiety may introduce hydrophobic characteristics that can limit solubility in purely aqueous environments.

In summary, while (4-iodophenyl)methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride;hydroiodide is likely to exhibit solubility in polar solvents, its overall behavior can vary significantly depending on environmental conditions. This highlights the intricate balance between polar and non-polar interactions at play within its structure.

Interesting facts

Exploring (4-iodophenyl)methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride;hydroiodide

(4-iodophenyl)methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride;hydroiodide, primarily known for its complex structure, presents a fascinating case for chemists interested in the interplay between organic chemistry and medicinal applications. This compound melds various structural elements that contribute to its unique properties and behaviors.

Key Features of the Compound:

  • Functional Groups: The presence of the 4-iodophenyl group significantly enhances the compound’s reactivity due to iodine’s capacity for participating in electrophilic substitution reactions.
  • Norbornane Framework: The 1,7,7-trimethylnorbornan-2-yl section introduces a bicyclic structure, making it important for studying stereochemistry and strain in organic molecules.
  • Quaternary Ammonium Nature: As a quaternary ammonium compound, this structure exhibits interesting ionic characteristics, which can influence its solubility and interaction with biological membranes.

This compound showcases the importance of both iodine and quaternary nitrogen in drug design, particularly in developing agents with antimicrobial and antiviral properties. According to recent studies, quaternary ammonium compounds often exhibit significant antibacterial activity, indicating that this compound might be of interest in pharmaceutical research.

Moreover, the presence of hydroiodide enhances the compound's stability and can influence its effectiveness in various applications. Researchers continually explore compounds like this one for their potential roles in sustainable chemistry and material science, particularly as we seek to create greener alternatives in chemical synthesis. The application of such compounds can stretch into industries ranging from pharmaceuticals to agriculture, making them a topic of continuous investigation and intrigue.

In conclusion, the multidimensional aspects of (4-iodophenyl)methyl-(1,7,7-trimethylnorbornan-2-yl)ammonium;chloride;hydroiodide render it a compound worth studying, promising to unveil further insights into potent new materials and applications.

Synonyms
(+-)-endo-N-(p-Iodobenzyl)-2-bornanamine hydrochloride
24652-90-2
2-BORNANAMINE, N-(p-IODOBENZYL)-, HYDROCHLORIDE, endo-(+-)-
RefChem:256681