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2,6-Diiodo-4-nitrophenol

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Identification
Molecular formula
C6H3I2NO3
CAS number
6631-99-0
IUPAC name
2,6-diiodo-4-nitro-phenol
State
State

At room temperature, 2,6-diiodo-4-nitrophenol is typically found as a solid. It is somewhat volatile and can sublimate, especially under reduced pressure.

Melting point (Celsius)
135.00
Melting point (Kelvin)
408.15
Boiling point (Celsius)
354.00
Boiling point (Kelvin)
627.15
General information
Molecular weight
408.92g/mol
Molar mass
408.9180g/mol
Density
3.0590g/cm3
Appearence

2,6-Diiodo-4-nitrophenol is typically a crystalline solid. The crystals are usually a yellow to pale orange color, reflecting the presence of the nitro group which often imparts color to organic compounds.

Comment on solubility

Solubility of 2,6-diiodo-4-nitro-phenol

When discussing the solubility of 2,6-diiodo-4-nitro-phenol, several key points come to mind:

  • Polar vs Non-Polar: 2,6-diiodo-4-nitro-phenol is generally categorized as a polar compound due to the presence of the nitro group and hydroxyl group, which tend to interact favorably with polar solvents such as water.
  • Water Solubility: While its polar characteristics imply a certain degree of water solubility, the presence of bulky iodine atoms can hinder this, leading to limited solubility in water.
  • Solubility in Organic Solvents: This compound tends to exhibit greater solubility in organic solvents like ethanol or dichloromethane, owing to its hydrophobic regions, primarily introduced by the iodine substituents.
  • Temperature Influence: The solubility may also vary with temperature; typically, increasing the temperature can enhance solubility in organic solvents.
  • Practical Implications: Such solubility characteristics are crucial for applications in synthesis and extraction, making knowledge of its behavior in different solvents essential for chemists.

The complexity of solubility in 2,6-diiodo-4-nitro-phenol illustrates the intricate balance between functional groups and molecular structure. Therefore, understanding this compound's solubility aids in its effective utilization in various chemical processes.

Interesting facts

Interesting Facts about 2,6-Diiodo-4-nitro-phenol

2,6-Diiodo-4-nitro-phenol is a fascinating compound known for its unique chemical structure and properties. Here are some intriguing facts about this compound:

  • Novelty in Nature: This compound is a derivative of phenol, featuring both nitro and iodo substituents on the aromatic ring, which significantly enhances its reactivity and makes it a potential candidate for further synthetic applications.
  • Potential Applications: Its unique combination of functional groups may allow it to act as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, showcasing its versatility in chemistry.
  • Research Interest: Scientists are increasingly interested in studying compounds like 2,6-diiodo-4-nitro-phenol due to their potential role in understanding environmental impacts and biological interactions. Compounds with halogen substitutions are often studied for their antibacterial and antifungal properties.
  • Environmental Impact: The presence of iodine in its structure suggests that it may have implications for environmental chemistry. Iodinated phenolic compounds can behave differently in biological systems compared to their non-iodinated counterparts.
  • Structural Complexity: The distribution of the nitro and iodo groups provides insight into electronic effects within the compound. The electron-withdrawing nitro group can influence the overall reactivity and stability of the compound's aromatic system.

The study of 2,6-diiodo-4-nitro-phenol exemplifies the rich interplay of organic chemistry and its applications in synthetic methods. As researchers delve deeper, who knows what new applications or properties may be uncovered!

Synonyms
2,6-Diiodo-4-nitrophenol
305-85-1
DISOPHENOL
Phenol, 2,6-diiodo-4-nitro-
Diisophenol
Syngamix
Ancylol
Disofen
Iodofen
Iodophen
2,6-diiod-4-nitrophenol
2,6-diiodo-4-nitro-phenol
EINECS 206-170-4
39S5ZJ6SYN
BRN 2052233
DISOPHEN
DTXSID4046573
DISOPHENOL [MI]
2,6-Diiod-4-nitrophenol [IUPAC]
NSC-94733
DISOPHENOL [MART.]
DTXCID2026573
CHEBI:81727
4-06-00-01368 (Beilstein Handbook Reference)
NSC 94733
NCGC00166241-01
DISOPHENOL (MART.)
2,6-Diiod-4-nitrophenol (IUPAC)
C6H3I2NO3
UNII-39S5ZJ6SYN
Devonea
MFCD00007335
4-nitro-2,6-diiodophenol
Phenol,6-diiodo-4-nitro-
WLN: WNR DQ CI EI
SCHEMBL205059
CHEMBL1361334
2,6-DIIDO-4-NITROPHENOL
NSC94733
Tox21_112367
STL573814
AKOS005263743
NCGC00166241-02
AS-55199
CAS-305-85-1
DB-005895
CS-0186524
NS00028944
C18393
EN300-395906
Y11298
SR-01000883707
SR-01000883707-1
Q27155583
InChI=1/C6H3I2NO3/c7-4-1-3(9(11)12)2-5(8)6(4)10/h1-2,10
206-170-4