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4-Hydroxy-3-iodo-5-nitrobenzonitrile

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Identification
Molecular formula
C7H3IN2O3
CAS number
261951-54-0
IUPAC name
4-hydroxy-3-iodo-5-nitro-benzonitrile
State
State

At room temperature, this compound is typically in a solid state.

Melting point (Celsius)
202.00
Melting point (Kelvin)
475.15
Boiling point (Celsius)
0.00
Boiling point (Kelvin)
0.00
General information
Molecular weight
319.01g/mol
Molar mass
319.0210g/mol
Density
2.1000g/cm3
Appearence

4-Hydroxy-3-iodo-5-nitrobenzonitrile typically appears as a solid compound. Its color ranges from off-white to light yellow, depending on impurities and the specific batch. The solid form can be either crystalline or powdery.

Comment on solubility

Solubility of 4-Hydroxy-3-iodo-5-nitro-benzonitrile

The solubility of 4-hydroxy-3-iodo-5-nitro-benzonitrile can be characterized by several key factors that influence its ability to dissolve in various solvents. It is important to consider the following aspects:

  • Polarity: This compound contains several functional groups, notably hydroxyl (–OH) and nitro (–NO2), which enhance its polarity. Polar solvents such as water may offer limited solubility, though the presence of the aromatic ring may restrict complete dissolution.
  • Hydrogen Bonding: The –OH group can participate in hydrogen bonding, which may influence solubility in polar environments. This can make the compound more soluble in hydrogen-bonding solvents, such as alcohols.
  • Temperature Effects: Solubility often increases with temperature. Thus, heating a solution could improve the dissolution of 4-hydroxy-3-iodo-5-nitro-benzonitrile in appropriate solvents.
  • Choice of Solvent: While it may show some solubility in water, organic solvents such as ethanol, acetone, or dimethyl sulfoxide (DMSO) could prove more effective due to their compatibility with both the polar and non-polar portions of the molecule.

In conclusion, the solubility of 4-hydroxy-3-iodo-5-nitro-benzonitrile is significantly influenced by its functional groups, the medium used, and environmental conditions. Understanding these characteristics is crucial for applications in chemical synthesis and formulation. As the saying goes, “like dissolves like,” and this encapsulates the essence of how solubility works for this compound.

Interesting facts

Interesting Facts about 4-Hydroxy-3-iodo-5-nitro-benzonitrile

4-Hydroxy-3-iodo-5-nitro-benzonitrile, often abbreviated as HINB, is a fascinating chemical compound with applications in various fields of research and industry. Here are some intriguing insights into this compound:

  • Aromatic Compound: HINB belongs to the family of aromatic compounds, which means it has a stable ring structure that imparts unique reactivity and stability characteristics.
  • Importance of Functional Groups: The presence of the hydroxyl group (-OH) and the nitro group (-NO2) suggests this compound can participate in hydrogen bonding and serve as a potential electrophile in chemical reactions, making it valuable in synthesis.
  • Medicinal Chemistry: Compounds like HINB with nitro and iodine functionalities have been studied for their biological activities. These substitutions can alter their pharmacological properties, leading to potential therapeutic applications.
  • Colorimetric Reactions: Due to the presence of the nitro group, HINB can engage in colorimetric reactions, which could be useful in analytical chemistry as a detectable marker or indicator in various chemical assays.
  • In Environment Studies: The study of such compounds also extends into environmental chemistry, where their stability and reactivity can influence environmental toxicity and degradation in ecosystems.
  • Research Applications: HINB can serve as a precursor in the game of organic synthesis, offering routes to create more complex structures that are essential for developing new materials or pharmaceuticals.

In summary, 4-hydroxy-3-iodo-5-nitro-benzonitrile is not just a chemical entity; it embodies the intricate relationship between molecular structure and function, opening doors to further research and application possibilities in multiple scientific domains.

Synonyms
Nitroxynil
Nitroxinil
Nitroxinilo
Nitroxinil [INN]
Nitroxinilum
Deldrax
Nitroxinilum [INN-Latin]
Nitroxinilo [INN-Spanish]
CCRIS 5743
Nitroxinil [INN:BAN]
EINECS 216-884-8
Nitroxinil (INN)
Deldrax (TN)
UNII-9L0EXQ7125
BRN 2213717
9L0EXQ7125
NITROXYNIL [MI]
NITROXINIL [MART.]
Trodax [veterynary] (TN)
DTXSID9075117
Nitroxinilum (INN-Latin)
Nitroxinilo (INN-Spanish)
NITROXINIL (MART.)
Trodax (veterynary)
DTXCID4035413
216-884-8
sgkgvabhdaqajo-uhfffaoysa-n
1689-89-0
4-Hydroxy-3-iodo-5-nitrobenzonitrile
BENZONITRILE, 4-HYDROXY-3-IODO-5-NITRO-
Dovenix
MFCD00070776
C7H3IN2O3
4-cyano-2-iodo-6-nitrophenol
4-Hydroxy-3-iodo-5-nitro-benzonitrile
MLS006011503
SCHEMBL166956
CHEMBL2104730
ALBB-028654
BCP13892
AKOS000276265
AKOS040755614
AC-9329
FN31895
HY-W049875
KS-1307
SMR000797772
SY110145
Nitroxynil 1000 microg/mL in Acetonitrile
CS-0102838
NS00014213
EN300-55806
D08278
Nitroxinil, VETRANAL(TM), analytical standard
AS-871/43475540
SR-01000944912
Q2680251
SR-01000944912-1
BRD-K23850772-001-01-0
Z839048042