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4-Methoxy-2-nitrophenol

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Identification
Molecular formula
C7H7NO4
CAS number
500-57-4
IUPAC name
4-methoxy-2-nitro-phenol
State
State

At room temperature, 4-Methoxy-2-nitrophenol is typically found in a solid state. Its crystalline form makes it stable under standard conditions, though it should be stored in a cool, dry place to maintain its integrity.

Melting point (Celsius)
84.00
Melting point (Kelvin)
357.15
Boiling point (Celsius)
315.80
Boiling point (Kelvin)
588.95
General information
Molecular weight
169.14g/mol
Molar mass
169.1480g/mol
Density
1.3330g/cm3
Appearence

4-Methoxy-2-nitrophenol appears as a crystalline solid. It has a pale yellow color typical of nitro compounds, and it may reflect light, giving it a slightly lustrous appearance. The compound can also exhibit slight hygroscopic characteristics, absorbing moisture from the environment.

Comment on solubility

Solubility of 4-methoxy-2-nitro-phenol

4-methoxy-2-nitro-phenol, with the chemical formula C7H7N1O4, exhibits interesting solubility characteristics that are important for its applications in various chemical processes.

Key points about its solubility:

  • In general, 4-methoxy-2-nitro-phenol is moderately soluble in organic solvents, such as ethanol and ether.
  • Its solubility in water is limited; however, it can be influenced by factors such as temperature and pH.
  • Due to the presence of both a methoxy group and a nitro group, the compound may engage in hydrogen bonding, which impacts its interaction with solvents.

In summary, while 4-methoxy-2-nitro-phenol shows a preference for organic solvents, its behavior in aqueous environments can vary, making it a fascinating compound for studies regarding solubility dynamics.

Interesting facts

Interesting Facts about 4-methoxy-2-nitro-phenol

4-methoxy-2-nitro-phenol, also known as 4-nitro-o-cresol, is a fascinating compound in the realm of organic chemistry that belongs to the class of nitrophenols. Here are some compelling facts about this compound:

  • Functional Groups: This compound contains both nitro (–NO2) and methoxy (–OCH3) functional groups, which contribute to its unique reactivity and properties.
  • Applications: It is widely studied for its utility in synthesizing various chemicals, particularly in the production of herbicides and insecticides. Additionally, it serves as an intermediate in the manufacture of dyes and pharmaceuticals.
  • Toxicity: As with many nitrophenols, 4-methoxy-2-nitro-phenol exhibits acute toxicity and environmental concerns, emphasizing the importance of handling it with care in laboratory settings.
  • Research Insights: Studies have suggested that the electronic structure of this compound makes it an interesting subject for exploring electron-sharing mechanisms and reactivity patterns in organic reactions.
  • Historical Significance: Nitrophenols have a long history in chemical research, including studies of their effects on biological systems, which paved the way for advances in both organic chemistry and toxicology.

Understanding the properties and applications of 4-methoxy-2-nitro-phenol not only enriches our knowledge of aromatic compounds but also underscores the intricate balance between chemical utility and safety in the field of chemistry.

Synonyms
1568-70-3
Phenol, 4-methoxy-2-nitro-
DTXSID80166133
DTXCID0088624
ybugoacxdpduir-uhfffaoysa-n
4-METHOXY-2-NITROPHENOL
4-Hydroxy-3-nitroanisole
MFCD00024247
2-Nitro-4-methoxyphenol
4-methoxy-2-nitro-phenol
4-Methoxy-2-nitrophenol #
SCHEMBL182941
SCHEMBL8225900
4-Methoxy-2-nitrophenol, 98%
BAA56870
STL280178
AKOS000120535
CS-W017725
AC-25987
PS-10589
SY024430
DB-043332
M1257
EN300-20943