Skip to main content

4-Iododiphenyl

ADVERTISEMENT
Identification
Molecular formula
C12H9I
CAS number
1136-83-6
IUPAC name
1-iodo-4-phenyl-benzene
State
State

Solid at room temperature.

Melting point (Celsius)
84.00
Melting point (Kelvin)
357.15
Boiling point (Celsius)
297.00
Boiling point (Kelvin)
570.15
General information
Molecular weight
280.11g/mol
Molar mass
280.1070g/mol
Density
1.7470g/cm3
Appearence

White to off-white crystalline powder.

Comment on solubility

Solubility of 1-iodo-4-phenyl-benzene

1-iodo-4-phenyl-benzene, with its complex aromatic structure, exhibits interesting solubility characteristics. This compound is predominantly non-polar due to the extensive delocalization of electrons in its aromatic rings. Therefore, its solubility tends to favor non-polar solvents.

Solvent Preferences:

  • Non-polar solvents: 1-iodo-4-phenyl-benzene is more soluble in solvents such as hexane, toluene, and other hydrocarbons.
  • Polar solvents: Its solubility in polar solvents like water is very low, as the lack of polar functional groups in its structure hinders interaction with water molecules.

In summary, we can expect the solubility behavior of 1-iodo-4-phenyl-benzene to follow a general rule of thumb: like dissolves like. The non-polar nature of this compound means it does not mix well with polar solvents, and this can significantly limit its practical applications in aqueous environments.

Interesting facts

Exploring 1-Iodo-4-phenyl-benzene

1-Iodo-4-phenyl-benzene, also known as p-iodo biphenyl, is a fascinating organic compound that highlights the intricate world of aromatic chemistry. This compound is characterized by the presence of both an iodo substituent and a phenyl group on a biphenyl backbone, which opens up a variety of interesting applications and studies.

Key Features

  • Polarity: The iodine atom, being more electronegative, introduces a unique dipole in the molecular structure, influencing its reactivity and interactions with other substances.
  • Reactivity: The presence of the iodine atom makes this compound a potential precursor for further chemical synthesis, allowing for the formation of more complex structures.
  • Application in Materials Science: Compounds like 1-iodo-4-phenyl-benzene can serve as building blocks for organic semiconductors, which are crucial in fields like electronics and photonics.

Chemical Behavior

One of the most intriguing aspects of 1-iodo-4-phenyl-benzene is its reactivity in electrophilic substitution reactions. As it retains the stability of the biphenyl system, it offers pathways for various chemical modifications:

  • Halogenation: The compound can undergo halogenation to introduce additional halogen atoms.
  • Nucleophilic Substitution: Its iodine substituent can be easily replaced by nucleophiles, allowing for the introduction of different functional groups.

In Conclusion

In summary, 1-iodo-4-phenyl-benzene is a compound that not only showcases the beauty of aromatic chemistry but also serves as an important tool in synthetic organic chemistry. Its unique properties and reactivity make it a subject of interest for chemists seeking to develop new compounds with novel functionalities.

Synonyms
4-IODOBIPHENYL
1591-31-7
1,1'-Biphenyl, 4-iodo-
p-Iodobiphenyl
4-Biphenyl iodide
p-Phenyliodobenzene
4-Iododiphenyl
Biphenyl, 4-iodo-
AI3-15372
NSC 3791
EINECS 216-469-1
DTXSID7061807
Biphenyl, 4-iodo-(8CI)
DTXCID4035122
216-469-1
4-Iodo-1,1'-biphenyl
1-iodo-4-phenylbenzene
Monoiodobiphenyl
MFCD00019028
NSC-3791
4-Biphenylyl iodide
4-IODO-BIPHENYL
4-Iodobiphenyl, 97%
6AN2BA2TAV
1, 4-iodo-
1-iodanyl-4-phenyl-benzene
SCHEMBL45621
NXYICUMSYKIABQ-UHFFFAOYSA-
NSC3791
BCP06698
BBL002447
CX1310
STK325713
AKOS000275836
CS-W002119
FI10763
GS-3356
AC-22940
SY014973
I0785
NS00025181
EN300-18000
M24750
A810002
AE-848/30708050
InChI=1/C12H9I/c13-12-8-6-11(7-9-12)10-4-2-1-3-5-10/h1-9H