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1-Fluoro-4-iodobenzene

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Identification
Molecular formula
C6H4FI
CAS number
352-33-0
IUPAC name
1-fluoro-4-iodo-benzene
State
State

At room temperature, 1-Fluoro-4-iodobenzene is generally in a solid state. It can exist in crystalline form and is not typically encountered as a liquid unless heated above its melting point.

Melting point (Celsius)
39.00
Melting point (Kelvin)
312.15
Boiling point (Celsius)
205.00
Boiling point (Kelvin)
478.15
General information
Molecular weight
221.99g/mol
Molar mass
221.9920g/mol
Density
1.9179g/cm3
Appearence

1-Fluoro-4-iodobenzene typically appears as a pale yellow or yellowish crystalline solid. Its crystals can have a lustrous or shiny aspect, and the substance can appear more granular in its powdered form.

Comment on solubility

Solubility of 1-fluoro-4-iodo-benzene

The solubility of 1-fluoro-4-iodo-benzene (C6H4F I) is influenced by several factors, primarily its molecular structure and the presence of functional groups. Being an aromatic compound, it exhibits a degree of hydrophobicity, which typically results in lower solubility in water.

Here are some key points regarding its solubility:

  • Water Solubility: 1-fluoro-4-iodo-benzene is poorly soluble in water due to its hydrophobic aromatic ring and electron-withdrawing halogen atoms.
  • Organic Solvents: It shows good solubility in organic solvents such as ethanol, acetone, and benzene, where the nonpolar character can interact favorably.
  • Influence of Halogens: The presence of F and I introduces polar characteristics, which can slightly enhance solubility in some polar organic solvents compared to other fully non-polar compounds.

In summary, while 1-fluoro-4-iodo-benzene remains insoluble in water, it is more soluble in nonpolar and some polar organic solvents. Understanding these solubility characteristics can be crucial for its applications in synthesis and chemical reactions.

Interesting facts

Interesting Facts about 1-Fluoro-4-iodo-benzene

1-Fluoro-4-iodo-benzene is a fascinating aromatic halide that showcases the diverse functionalities of benzene derivatives. This compound integrates both fluorine and iodine substituents on the benzene ring, which introduces unique chemical properties and reactivity patterns. Here are some intriguing aspects of this molecule:

  • Halogen Chemistry: The presence of both fluorine and iodine creates a scenario of competitive reactivity, as these halogens exhibit different electronegativities and steric effects. Fluorine is highly electronegative, while iodine is relatively bulkier.
  • Pharmacological Applications: Compounds like 1-fluoro-4-iodo-benzene are of interest in medicinal chemistry. Their unique properties can influence how molecules interact in biological systems, making them potential candidates for drug design.
  • Material Science: This compound may also find applications in the development of polymers and materials. The presence of halogens can impart desirable characteristics such as flame resistance and enhanced thermal stability.
  • Synthesis Pathways: The synthesis of 1-fluoro-4-iodo-benzene typically involves nucleophilic substitution reactions that can yield diverse products, making it a valuable intermediate in organic synthesis.
  • Electronegativity Influence: The differing electronegativities of the fluorine and iodine atoms can result in interesting electronic effects, impacting the compound’s reactivity in electrophilic aromatic substitution reactions.

In summary, 1-fluoro-4-iodo-benzene embodies the intricate dance of chemistry where various factors interplay to yield compounds with significant applicability. As chemists continue to explore such derivatives, they contribute to advancements in fields like pharmaceuticals and materials science.

Synonyms
4-Fluoroiodobenzene
1-FLUORO-4-IODOBENZENE
352-34-1
p-Fluoroiodobenzene
Benzene, 1-fluoro-4-iodo-
4-Iodofluorobenzene
4-fluoro-1-iodobenzene
p-Iodofluorobenzene
1-IODO-4-FLUOROBENZENE
H2Z2C5X7RW
MFCD00001052
NSC-10280
benzene, 1-fluoro-4-iodo
1-fluoranyl-4-iodanyl-benzene
DTXSID7059854
1-Fluoro-4-iodobenzene (stabilized with Copper chip)
4-Fluoro-iodobenzene
1-fluoro-4-iodo-benzene
4-fluroiodobenzene
NSC4662
4-flouroiodobenzene
EINECS 206-522-7
4-iodo-fluorobenzene
NSC 10280
1-fluoro4-iodobenzene
1-Fluor-4-jod-benzol
4-fluoro-1-iodo-benzene
1-Iodo-4-fluoro-benzene
UNII-H2Z2C5X7RW
4-Fluoroiodobenzene, 99%
SCHEMBL1216
DTXCID0038960
CS-D1411
NSC-4662
NSC10280
AKOS005258233
AC-9717
GS-6799
SB66336
SY001127
DB-027416
F0237
NS00042105
EN300-54342
F0001-1020
206-522-7
Y8D