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1-Chloro-3-iodobenzene

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Identification
Molecular formula
C6H4ClI
CAS number
625-99-0
IUPAC name
1-chloro-3-iodo-benzene
State
State

At room temperature, 1-chloro-3-iodobenzene is in a liquid state.

Melting point (Celsius)
6.00
Melting point (Kelvin)
279.15
Boiling point (Celsius)
247.00
Boiling point (Kelvin)
520.15
General information
Molecular weight
221.45g/mol
Molar mass
221.4490g/mol
Density
1.9420g/cm3
Appearence

1-Chloro-3-iodobenzene is a colorless to pale yellow liquid. It appears as a liquid at room temperature and is known for its aromatic odor due to the benzene ring structure.

Comment on solubility

Solubility of 1-Chloro-3-iodo-benzene

1-Chloro-3-iodo-benzene, with the chemical formula C6H4ClI, is an aromatic compound characterized by the presence of both a chlorine and an iodine atom attached to the benzene ring. When discussing its solubility, we note the following key points:

  • Polar vs. Nonpolar: The presence of halogen atoms (Cl and I) introduces some polarity; however, the overall structure remains predominantly nonpolar due to the large benzene ring.
  • Solvent Compatibility: 1-Chloro-3-iodo-benzene does not dissolve well in polar solvents such as water but is more soluble in organic, nonpolar solvents like benzene, toluene, and chloroform.
  • Hydrophobic Interactions: The hydrophobic nature of the benzene ring contributes to lower solubility in polar environments. It is important to choose a solvent that minimizes these interactions for effective dissolution.

In summary, while 1-chloro-3-iodo-benzene exhibits limited solubility in polar solvents, it finds greater compatibility with nonpolar organic solvents, making it a compound of interest in synthetic organic chemistry where such solubility characteristics can be exploited.


Interesting facts

Interesting Facts about 1-Chloro-3-iodo-benzene

1-Chloro-3-iodo-benzene is a fascinating compound that belongs to the family of aromatic halogenated compounds. Here are some key points that highlight its significance:

  • Structural Diversity: The presence of both chlorine and iodine atoms on the benzene ring allows for diverse reactivity patterns. This makes it a valuable intermediate in the synthesis of various organic compounds.
  • Applications: 1-chloro-3-iodo-benzene is commonly utilized in the production of pharmaceuticals, agrochemicals, and specialized dyes, showcasing its versatility in multiple industries.
  • Reactivity: The halogen substituents significantly influence the electronic properties of the compound, leading to unique reaction pathways. For example, it exhibits reactivity in nucleophilic substitution reactions due to the polar nature of the C-X bonds.
  • Mechanism Insights: The bromination or iodination mechanism can provide insights into electrophilic aromatic substitution, illustrating the effects of electron-withdrawing and electron-donating groups on reactivity.
  • Environmental Concerns: With the growing emphasis on green chemistry, understanding the degradation pathway of halogenated compounds like 1-chloro-3-iodo-benzene is crucial, as they can pose environmental and health risks if not handled properly.

In conclusion, studying this compound not only enhances our understanding of organic reactions but also opens pathways to developing safer and more effective products in various fields.


Synonyms
1-Chloro-3-iodobenzene
Benzene, 1-chloro-3-iodo-
EINECS 210-920-6
NSC 32861
AI3-22030
DTXSID4060810
DTXCID2043379
210-920-6
inchi=1/c6h4cli/c7-5-2-1-3-6(8)4-5/h1-4
jmlwxcjxoydxrn-uhfffaoysa-n
625-99-0
3-CHLOROIODOBENZENE
m-Chloroiodobenzene
3-Iodochlorobenzene
3-Chloro-1-iodobenzene
m-Chlorophenyl iodide
1-Chloro-3-iodo-benzene
MFCD00001046
metachloroiodobenzene
NSC32861
m-chloro iodobenzene
3-chloro-iodobenzene
3-iodo-chlorobenzene
Chloro-3-iodobenzene
1-iodo-3-chloro-benzene
3-Chloroiodobenzene, 98%
SCHEMBL139812
1-chloranyl-3-iodanyl-benzene
NSC-32861
AKOS005254984
CS-W007365
BP-20201
DS-14649
FC139705
SY001074
DB-019124
NS00035089
EN300-131191
O10397
A833875
Z381540752