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(4-Nitrophenyl)phenyliodonium

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Identification
Molecular formula
C12H9INO2
CAS number
.
IUPAC name
(4-nitrophenyl)-phenyl-iodonium
State
State

At room temperature, (4-Nitrophenyl)phenyliodonium is generally found in a solid state, often in the form of crystalline powder or shards, depending on storage conditions.

Melting point (Celsius)
111.00
Melting point (Kelvin)
384.15
Boiling point (Celsius)
291.00
Boiling point (Kelvin)
564.15
General information
Molecular weight
375.11g/mol
Molar mass
375.1300g/mol
Density
2.1200g/cm3
Appearence

(4-Nitrophenyl)phenyliodonium commonly appears as a solid substance that can be detailed as crystalline. The solid's color may vary depending on its purity and form.

Comment on solubility

Solubility of (4-nitrophenyl)-phenyl-iodonium

The solubility of (4-nitrophenyl)-phenyl-iodonium, with its unique structure and functional groups, provides some interesting insights:

  • Polarity: The presence of the nitro group (–NO2) often increases polarity, potentially enhancing solubility in polar solvents like water.
  • Solvent Interactions: Due to its ionic nature, this compound may exhibit higher solubility in polar aprotic solvents or suitable organic solvents compared to nonpolar solvents.
  • Temperature Effects: Generally, solubility can increase at elevated temperatures, thus it is advisable to consider heating the solvent to facilitate dissolution.
  • pH Sensitivity: The ionization state can change with pH adjustments, which can significantly affect solubility.

In essence, while the compound may show variable solubility depending on the solvent and conditions, it is critical to experiment under controlled conditions to ascertain the optimal solubility profile. Remember, “the right conditions yield the best results”.

Interesting facts

Interesting Facts about (4-nitrophenyl)-phenyl-iodonium

(4-nitrophenyl)-phenyl-iodonium is a fascinating compound that showcases the intricate world of organoiodine chemistry. This compound features a unique structural framework that can be explored through various chemical applications.

Key Properties and Applications

  • Photo-cationic polymerization: This compound is often utilized as a photoinitiator in the field of polymer chemistry, contributing to the synthesis of high-performance materials upon exposure to light.
  • Electrophilic reactivity: The presence of the iodonium moiety imparts significant electrophilic characteristics, allowing this compound to act effectively in various nucleophilic substitution reactions.
  • Drug discovery: Iodonium compounds like this one have been explored within pharmaceutical research, providing valuable insights into potential drug candidates and therapeutic agents.

Chemical Behavior

The rich chemistry of (4-nitrophenyl)-phenyl-iodonium stems from its ability to easily release reactive iodonium cations. As noted by researchers, *"its versatility in synthetic applications can lead to pathways less accessible through traditional reagents."* This characteristic makes it a preferred choice for chemists looking to leverage its properties in cutting-edge chemical reactions.

Environmental Considerations

As with many organoiodine compounds, the environmental impact of (4-nitrophenyl)-phenyl-iodonium deserves attention. Chemistry students and scientists often advocate for research into sustainable alternatives and strategies to minimize environmental harm while maximizing utility.

In summary, (4-nitrophenyl)-phenyl-iodonium represents a vital component in modern organic chemistry, with applications ranging from materials science to pharmacology. Its multifaceted nature captures the interest of both researchers and students alike, making it a compound worth exploring further!

Synonyms
NSC86354
SCHEMBL426370
(p-Nitrophenyl)phenyliodonium-
SCHEMBL3872162
(4-nitrophenyl)-phenyl-iodonium
CHEMBL2009430
Iodonium, (p-nitrophenyl)phenyl-
Iodonium, (4-nitrophenyl)phenyl-
NCI60_041908
Hydroxy(4-(phenyl-lambda~3~-iodanyl)phenyl)azane oxide