Interesting facts
Interesting Facts about 2,4,6-Triiodophenol
2,4,6-Triiodophenol is a fascinating compound in the world of organic chemistry, renowned for its unique properties and applications. Here are some intriguing aspects of this compound:
- Structure and Stability: The compound contains three iodine atoms attached to the benzene ring, which significantly influences its chemical behavior and stability. The high electronegativity of iodine can confer special properties that make this compound very interesting for further study.
- Electron Donor Properties: The iodine atoms can act as electron-withdrawing groups, enhancing the compound's reactivity in various chemical reactions. It’s a prime example of how substituents influence the behavior of aromatic compounds.
- Applications in Research: 2,4,6-Triiodophenol is often used in research as a reagent in organic synthesis and as a color indicator. Its vibrant coloration makes it useful in various analytical applications.
- Antimicrobial Activity: Various studies suggest that 2,4,6-triiodophenol exhibits antimicrobial properties, making it a potential candidate for developing new antiseptic agents.
- Environmental Considerations: Given its iodine content, there are ongoing studies regarding the environmental impact and biodegradability of this compound. Understanding its fate in various ecosystems is essential for assessing safety.
- Historical Significance: This compound has a significant place in the historical development of synthetic organic chemistry, showcasing how scientists have leveraged halogenated compounds for functional innovations.
In summary, 2,4,6-triiodophenol serves multiple roles in science, from its structural importance in organic synthesis to its potential applications in medicine and environmental science. Its unique characteristics offer a rich field of study for chemists and researchers alike.
Synonyms
2,4,6-TRIIODOPHENOL
609-23-4
Phenol, 2,4,6-triiodo-
2,4,6-Trijodfenol
2,4,6-Trijodfenol [Czech]
NSC 2594
EINECS 210-186-7
BRN 2046861
9RB2R81A7U
DTXSID8022080
NSC-2594
DTXCID602080
Bobel 24
Bobel-24
2,4,6-TIP
210-186-7
inchi=1/c6h3i3o/c7-3-1-4(8)6(10)5(9)2-3/h1-2,10
TRIIODOPHENOL
2,4,6-Triiodo-phenol
MFCD00002179
CHEMBL81721
2,4,6-Triiodo-phenol(TIP)
UNII-9RB2R81A7U
2,6-Triiodophenol
Phenol,4,6-triiodo-
WLN: QR BI DI FI
SCHEMBL338137
2,4,6-Triiodophenol, 97%
NSC2594
AM-24
Tox21_303909
BDBM50301374
AKOS009031508
HY-W073687
NCGC00356970-01
AC-22931
AS-57147
CAS-609-23-4
FT158932
SY048671
DB-050519
CS-0106873
NS00006379
T0452
EN300-19379
D76670
BRD-K59013864-001-01-1
Q27272970
F8889-6052
Z104473672
2,4,6-Triiodophenol, certified reference material, TraceCERT(R)
Solubility of 2,4,6-Triiodophenol
2,4,6-triiodophenol, with the chemical formula C6H4I3O, exhibits some interesting solubility characteristics:
Overall, when discussing the solubility of this compound, it is essential to remember that its interactions with solvents can be influenced by various factors, making it important to consider the specific conditions of your experiment. As evidenced, the solvent environment plays a crucial role in determining how well this compound can be dissolved, calling for careful consideration in practical applications.