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Unknown Compound

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Identification
Molecular formula
C18H22I2O2
CAS number
.
IUPAC name
[4-(4-iodooxy-5-isopropyl-2-methyl-phenyl)-2-isopropyl-5-methyl-phenyl] hypoiodite
State
State

At room temperature, this compound's state would likely be solid due to the presence of aromatic and iodine groups.

Melting point (Celsius)
0.00
Melting point (Kelvin)
0.00
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
0.00g/mol
Molar mass
0.0000g/mol
Density
0.0000g/cm3
Appearence

The appearance of this compound is not specifically well-documented, given the complexity and specificity of its IUPAC name. Generally, iodide compounds show a wide range of appearances, including crystalline and powder forms. Further research would be necessary for a precise description.

Comment on solubility

Solubility of [4-(4-iodooxy-5-isopropyl-2-methyl-phenyl)-2-isopropyl-5-methyl-phenyl] hypoiodite

The solubility of [4-(4-iodooxy-5-isopropyl-2-methyl-phenyl)-2-isopropyl-5-methyl-phenyl] hypoiodite can often be predicted based on its structure and the presence of functional groups. Here are some key points to consider:

  • Polarity: Hypoiodite compounds contain polar bonds due to the presence of iodine, which affects their solubility in various solvents.
  • Solvent Dependence: This compound may exhibit high solubility in polar solvents like water and ethanol, but low solubility in non-polar organic solvents such as hexane.
  • Hydrophilic vs. Hydrophobic: The presence of the isopropyl and methyl groups generally suggests a hydrophobic character that could limit solubility in aqueous solutions.
  • Hydrogen Bonding: The ability of the compound to form hydrogen bonds can also influence solubility, particularly in polar solvents where interactions may enhance solubility.

In conclusion, while the precise solubility of [4-(4-iodooxy-5-isopropyl-2-methyl-phenyl)-2-isopropyl-5-methyl-phenyl] hypoiodite can vary, understanding these factors is crucial for predicting its behavior in solution. As with any compound, conducting experimental solubility tests in a variety of solvents will yield the most accurate results.

Interesting facts

Interesting Facts About 4-(4-Iodooxy-5-isopropyl-2-methyl-phenyl)-2-isopropyl-5-methyl-phenyl Hypoiodite

This intriguing compound, known as 4-(4-iodooxy-5-isopropyl-2-methyl-phenyl)-2-isopropyl-5-methyl-phenyl hypoiodite, showcases the fascinating world of organic chemistry and the versatility of halogenated compounds.

Chemical Significance

  • Hypoiodite Group: The presence of the hypoiodite (–OI) functional group serves as a powerful oxidizing agent, often utilized in various chemical reactions, including iodination.
  • Halogen Chemistry: Halogens, like iodine, play a crucial role in medicinal chemistry. Iodinated compounds often exhibit unique biological activities, making them valuable in pharmaceuticals.
  • Synthesis Potential: The complex structure of this compound suggests potential applications in organic synthesis, specifically in creating novel materials or intermediates in drug development.

Applications in Research

Researchers are exploring compounds like this one for their potential applications:

  • In medicinal chemistry, where iodine's presence is linked to enhancing biological properties of therapeutic agents.
  • In materials science, where halogenated compounds can improve the stability and performance of polymers and other materials.
  • As an oxidizing agent in various organic reactions, influencing reaction pathways and product formation.

Fascinating Facts

Here are some additional tidbits that make this compound particularly interesting:

  • Structural Complexity: The intricate arrangement of isopropyl and methyl groups highlights the structural diversity that can arise in organic molecules.
  • Reactivity: Compounds featuring hypoiodite groups often engage in various chemical reactions, including electrophilic substitutions and oxidations.
  • Interdisciplinary Interest: The study of such compounds crosses multiple scientific disciplines, from synthetic organic chemistry to pharmacology and materials science.

In summary, 4-(4-iodooxy-5-isopropyl-2-methyl-phenyl)-2-isopropyl-5-methyl-phenyl hypoiodite embodies the complexity and potential of halogenated organic compounds, inspiring ongoing research and innovation in various fields.

Synonyms
THYMOL IODIDE
552-22-7
Iodothymol
Iodistol
Iodohydromol
Annidalin
Iothymol
Lothymol
Thymiode
Thymiodol
Thymodin
Thymotol
Aristol
Iodosol
Iosol
Diiododithymol
Bithymol diiodide
Dithymol diiodide
Iodothymol (VAN)
Thymol iodide [NF]
A51HJM3XSU
HSDB 867
DTXSID3046081
NSC 2222
NSC-2222
EINECS 209-007-5
THYMOL IODIDE [HSDB]
THYMOL IODIDE [VANDF]
THYMOL IODIDE [WHO-DD]
DTXCID1026081
4,4'-Bis(iodooxy)-2,2'-dimethyl-5,5'-bis(1-methylethyl-1,1'-biphenyl
1,1'-Biphenyl, 4,4'-bis(iodooxy)-2,2'-dimethyl-5, 5'-bis(1-methylethyl)-
5,5'-Diisopropyl-2,2'-dimethylbiphenyl-4,4'-diyl dihypoiodite
4,4'-bis(I4,4'-Bodooxy)-2,2'-dimethyl-5,5'-bis(1-methylethyl-1,1'-biphenyl
Hypoiodous acid, 2,2'-dimethyl-5,5'-bis(1-methylethyl)(1,1'-biphenyl)-4,4'-diyl ester
Hypoiodous acid, 2,2'-dimethyl-5,5'-bis(1-methylethyl)[1,1'-biphenyl]-4,4'-diyl ester
Hypoiodous acid, I,I'-(2,2'-dimethyl-5,5'-bis(1-methylethyl)(1,1'-biphenyl)-4,4'-diyl) ester
Hypoiodous acid, I,I'-[2,2'-dimethyl-5,5'-bis(1-methylethyl)[1,1'-biphenyl]-4,4'-diyl] ester
Thymol iodide (8CI)
5,5'Diisopropyl2,2'dimethylbiphenyl4,4'diyl dihypoiodite
4,4'Bis(iodooxy)2,2'dimethyl5,5'bis(1methylethyl1,1'biphenyl
1,1'Biphenyl, 4,4'bis(iodooxy)2,2'dimethyl5, 5'bis(1methylethyl)
Hypoiodous acid, 2,2'dimethyl5,5'bis(1methylethyl)(1,1'biphenyl)4,4'diyl ester
THYMOLIODIDE
[4-(4-iodooxy-2-methyl-5-propan-2-ylphenyl)-5-methyl-2-propan-2-ylphenyl] hypoiodite
NCGC00159504-02
CAS-552-22-7
UNII-A51HJM3XSU
thymol-iodide
SCHEMBL467308
CHEMBL1482931
NSC2222
SHOKWSLXDAIZPP-UHFFFAOYSA-N
HY-B1796
Tox21_111723
MFCD00026409
AKOS024319269
Tox21_111723_1
NCGC00159504-03
NCGC00159504-04
BS-28664
DA-78451
CS-0013832
NS00021210
G12082
SBI-0654151.0001
SR-01000883682
SR-01000883682-1
BRD-K36617478-001-01-5
Q27273640
1, 4,4'-bis(iodooxy)-2,2'-dimethyl-5,5'-bis(1-methylethyl)-
4,4'-Bis(iodooxy)-2,2'-dimethyl-5,5'-bis(1-methylethyl)-1,1'-biphenyl
Hypoiodous acid,2'-dimethyl-5,5'-bis(1-methylethyl)[1,1'-biphenyl]-4,4'-diyl ester