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2-Iodoethylbenzene

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Identification
Molecular formula
C8H9I
CAS number
3240-34-4
IUPAC name
2-iodoethylbenzene
State
State

At room temperature, 2-iodoethylbenzene is in a liquid state.

Melting point (Celsius)
-31.00
Melting point (Kelvin)
242.15
Boiling point (Celsius)
228.00
Boiling point (Kelvin)
501.15
General information
Molecular weight
232.06g/mol
Molar mass
232.0630g/mol
Density
1.7050g/cm3
Appearence

2-Iodoethylbenzene is a colorless to pale yellow liquid. It is typically clear and can vary slightly in shade depending on the purity of the sample.

Comment on solubility

Solubility of 2-iodoethylbenzene

2-iodoethylbenzene, known for its intriguing chemical properties, exhibits unique solubility characteristics that can significantly influence its use in various applications. Here's a deeper look at the solubility of this compound:

  • Solvent Compatibility: 2-iodoethylbenzene is typically more soluble in organic solvents such as acetone, ethanol, and ether. This is largely due to its hydrophobic nature from the benzene ring and the iodine substituent.
  • Water Solubility: In contrast, the solubility of 2-iodoethylbenzene in water is minimal. The compound's structure does not favor interactions with polar water molecules, making it poorly soluble in aqueous solutions.
  • Effect of Temperature: It is worth noting that the solubility of organic compounds like 2-iodoethylbenzene can be affected by temperature. Generally, an increase in temperature may enhance solubility in organic solvents.
  • Applications: Understanding the solubility of 2-iodoethylbenzene is crucial for its application in synthesis and extraction processes within organic chemistry, as solubility determines its reactivity and usefulness in various reactions.

In summary, while 2-iodoethylbenzene is not water-soluble, it shows a favorable solubility profile in organic solvents, allowing for diverse applications in the field of chemistry.

Interesting facts

Interesting Facts about 2-Iodoethylbenzene

2-Iodoethylbenzene, a fascinating organic compound, belongs to the family of aryl halides. This compound features an iodo group and an ethyl group attached to a benzene ring, making it quite unique in its structure. Here are some intriguing aspects of 2-iodoethylbenzene:

  • Chemical Reactivity: The presence of the iodine atom makes 2-iodoethylbenzene a valuable intermediate in organic synthesis. Iodine is a good leaving group, facilitating nucleophilic substitution reactions.
  • Applications in Synthesis: This compound is often utilized in the synthesis of various pharmaceuticals and agrochemicals. Its distinctive structure allows for the incorporation of more complex biological molecules.
  • Drug Discovery: The compound and its derivatives are of great interest in medicinal chemistry. Research has shown that certain iodoalkylbenzenes exhibit antitumor and anti-inflammatory properties.
  • Scientific Importance: 2-Iodoethylbenzene serves as a model compound in studies regarding nucleophilic aromatic substitution, helping scientists to explore reaction mechanisms and kinetics.
  • Environmental Considerations: As with many halogenated compounds, there is ongoing research into the environmental impact of 2-iodoethylbenzene, including its persistence and potential for bioaccumulation.

In summary, 2-iodoethylbenzene is not just another chemical compound; it plays a crucial role in organic synthesis and medicinal chemistry, making it a significant subject of study in the field of chemistry. Its versatility and reactivity open doors to numerous applications, keeping it relevant in scientific research.

Synonyms
Benzene, (2-iodoethyl)-
AI3-52406
(2-IODOETHYL)BENZENE
17376-04-4
2-Iodoethylbenzene
2-Phenylethyl iodide
Phenethyl iodide
Iodoethyl benzene
MFCD00039408
(2-iodoethyl) benzene
(2-Iodoethyl)-benzene
.beta.-Phenethyl iodide
DTXSID5025447
phenethyliodide
p-iodoethylbenzene
phenylethyl iodide
4-iodoethylbenzene
(2-iodo-ethyl)benzene
.beta.-Phenylethyl iodide
(2-Iodoethyl)benzene, 97%
SCHEMBL172979
DTXCID305447
SCHEMBL2891655
CHEMBL1472377
Tox21_200053
AKOS009157873
CS-W012940
NCGC00091564-01
NCGC00091564-02
NCGC00257607-01
(2-Iodoethyl)benzene, stabilized over Cu
AS-57952
SY050349
CAS-17376-04-4
DB-043958
I0521
NS00096234
D70924