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4-Nitroiodobenzene

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Identification
Molecular formula
C6H4INO2
CAS number
636-98-6
IUPAC name
1-iodo-4-nitro-benzene
State
State

At room temperature, 4-nitroiodobenzene exists as a solid.

Melting point (Celsius)
171.00
Melting point (Kelvin)
444.15
Boiling point (Celsius)
305.00
Boiling point (Kelvin)
578.15
General information
Molecular weight
265.01g/mol
Molar mass
265.0120g/mol
Density
2.0330g/cm3
Appearence

4-Nitroiodobenzene appears as a light yellow to pale brown crystalline solid. It is known for its distinctive coloring, which may vary slightly depending on its purity and the conditions of observation.

Comment on solubility

Solubility of 1-iodo-4-nitro-benzene

1-iodo-4-nitro-benzene, with the chemical formula C6H4INO2, exhibits specific solubility characteristics due to its unique structure and functional groups. Understanding its solubility can be crucial for various applications in organic synthesis and chemical analysis.

Solubility Characteristics:

  • Polar vs. Nonpolar: 1-iodo-4-nitro-benzene is mainly a nonpolar compound because of its aromatic structure, which impacts its interactions with solvents.
  • Solvents:
    • Organic solvents: It is more soluble in organic solvents such as chloroform, ethyl acetate, and benzene.
    • Aqueous solutions: The solubility in water is quite limited due to the nonpolar characteristics, making it largely insoluble.
  • Functional Groups: The presence of the nitro group (-NO2) may impart some polar characteristics, but the dominant nonpolar properties seem to prevail.

In conclusion, one can summarize that 1-iodo-4-nitro-benzene is mainly soluble in nonpolar solvents and exhibits limited solubility in polar environments like water. When considering its application, understanding these solubility properties is vital for selecting the appropriate solvent systems.

Interesting facts

Exploring 1-Iodo-4-Nitro-Benzene

1-Iodo-4-nitro-benzene is a fascinating aromatic compound that presents intriguing opportunities for study and application in the field of chemistry. Known for its versatility, this compound holds significant importance in various chemical reactions and processes. Here are some interesting facts about it:

  • Nitro group influence: The presence of the nitro group (–NO2) not only modifies the electronic characteristics of the benzene ring but also enhances the compound's reactivity compared to non-nitro substituted benzenes.
  • Functional group synergy: The combination of the iodo (–I) and nitro (–NO2) groups allows for unique synthetic pathways. For instance, it can be used in nucleophilic substitution reactions, where the iodo group can easily be replaced by other nucleophiles.
  • Applications in synthesis: 1-Iodo-4-nitro-benzene serves as a vital intermediate in the synthesis of pharmaceuticals and agrochemicals. Its utility in creating biologically active compounds makes it a valuable building block in organic synthesis.
  • Research interest: This compound attracts attention in material science as well, particularly for developing materials with specific electronic or optical properties.

Scientific Remarks

As a chemist or a student, understanding the role of halogenated and nitro compounds like 1-iodo-4-nitro-benzene can broaden your perspective on chemical reactions. The interplay of various functional groups and their effects on reactivity flow enable innovative approaches to synthesizing complex molecules. In the words of renowned chemist Henry Ford: “The only real mistake is the one from which we learn nothing.” Every reaction involving this compound can lead to valuable insights and advancements in the field.


Overall, 1-iodo-4-nitro-benzene stands out for its chemical properties and wide-ranging applications, and it is a testament to the complexity and beauty of organic chemistry.

Synonyms
1-Iodo-4-nitrobenzene
4-IODONITROBENZENE
Benzene, 1-iodo-4-nitro-
NSC 9794
EINECS 211-272-7
AI3-08878
DTXSID7060914
pIodonitrobenzene
pNitroiodobenzene
4Iodonitrobenzene
4Nitroiodobenzene
pNitrophenyl iodide
Benzene, 1iodo4nitro
DTXCID1044019
211-272-7
inchi=1/c6h4ino2/c7-5-1-3-6(4-2-5)8(9)10/h1-4
scccfnjtcdslcy-uhfffaoysa-n
636-98-6
p-Iodonitrobenzene
p-Nitroiodobenzene
4-Nitroiodobenzene
p-Nitrophenyl iodide
30306-69-5
4-iodo-1-nitrobenzene
1-iodo-4-nitro-benzene
MFCD00007299
4-nitrophenyl iodide
4-Iodonitrobenzene-13C6
NSC-9794
4-iodo-nitrobenzene
para-nitro iodo-benzene
NSC9794
para-iodonitrobenzene
p-iodo-nitro-benzene
1-Nitro-4-iodobenzene
NH3N3MPW9D
SCHEMBL60337
ghl.PD_Mitscher_leg0.938
1-Iodo-4-nitrobenzene, 98%
SCHEMBL13578687
BCP14439
STR06257
STK335825
AKOS000120996
FI70119
AC-22935
DB-014512
I0064
NS00035530
1-iodo-4-nitro-benzen;4-Iodo-1-nitrobenzene
EN300-17392
A20880
Q63399511
Z56924538