Skip to main content

Glycidyl 4-nitrophenyl ether

ADVERTISEMENT
Identification
Molecular formula
C9H9NO4
CAS number
13349-82-1
IUPAC name
2-[(4-nitrophenoxy)methyl]oxirane
State
State
Glycidyl 4-nitrophenyl ether is typically found in a liquid state at room temperature. However, it can crystallize into a solid form if exposed to lower temperatures or stored improperly.
Melting point (Celsius)
24.00
Melting point (Kelvin)
297.15
Boiling point (Celsius)
308.00
Boiling point (Kelvin)
581.15
General information
Molecular weight
195.18g/mol
Molar mass
195.1750g/mol
Density
1.2920g/cm3
Appearence

Glycidyl 4-nitrophenyl ether typically appears as a yellowish to light brown liquid. The compound may crystallize into solid form under certain conditions, showing its polymorphic capabilities. It is moderately viscous and is characterized by a faint aromatic odor.

Comment on solubility

Solubility of 2-[(4-nitrophenoxy)methyl]oxirane

The solubility of 2-[(4-nitrophenoxy)methyl]oxirane can be understood through a combination of its structural characteristics and the polarity of the molecule. This compound, also known as a glycidyl ether, features a nitrophenyl group, which can significantly influence its solubility in different solvents.

Key Factors Affecting Solubility:

  • Polarity: The presence of the –NO2 group in the nitrophenyl moiety increases the overall polarity of the molecule, enhancing its solubility in polar solvents.
  • Hydrogen Bonding: The ability of the oxirane ring to engage in hydrogen bonding with polar solvents, such as water, may increase its solubility under certain conditions.
  • Solvent Type: This compound is expected to show better solubility in organic solvents like acetone or ethanol, while its solubility in water might be limited compared to more polar compounds.

It is important to note that the solubility behavior of 2-[(4-nitrophenoxy)methyl]oxirane can vary depending on temperature and the presence of other chemicals. As a general rule, the following statement holds:

A compound's solubility is dictated by its interaction with the solvent's properties.

In summary, while 2-[(4-nitrophenoxy)methyl]oxirane may exhibit varying solubility in different media, the impacting factors primarily revolve around its molecular structure and the nature of the solvent. Therefore, experimentation and empirical data are essential to determine its exact solubility profile in practical applications.

Interesting facts

Interesting Facts about 2-[(4-nitrophenoxy)methyl]oxirane

2-[(4-nitrophenoxy)methyl]oxirane is a fascinating compound that demonstrates the intricate relationship between structure and function in organic chemistry. As a member of the epoxide family, this compound features a three-membered cyclic ether that is characterized by unique reactivity patterns. Below are some compelling insights into this compound:

  • Functional Groups: The presence of both the nitro group and the epoxide functionality makes this compound particularly interesting, as the nitro group can influence the reactivity and polarity of the molecule.
  • Reactivity: The epoxide group is strained and highly reactive, making it an excellent candidate for various chemical reactions, including nucleophilic attack which can lead to the formation of more complex structures.
  • Applications: Compounds like 2-[(4-nitrophenoxy)methyl]oxirane are often used in the synthesis of polymers, pharmaceuticals, and agrochemicals, showcasing their versatility in multiple fields.
  • Biodegradability: Some epoxides have been studied for their potential environmental impact, as they can undergo hydrolysis, which may lead to less harmful products in aquatic systems.
  • Structure-Activity Relationship (SAR): The incorporation of the nitrophenoxy moiety is of particular interest for medicinal chemistry, as variations in substituent groups can profoundly affect biological activity.

In conclusion, 2-[(4-nitrophenoxy)methyl]oxirane not only embodies the principles of organic reactivity but also highlights the significance of modifying chemical structures for improved functionality. As scientists continue to explore its properties, this compound serves as a reminder of the creative potential within chemical research.

Synonyms
1,2-epoxy-3-(4-nitrophenoxy)propane
2-[(4-Nitrophenoxy)methyl]oxirane
1,2-Epoxy-3-(p-nitrophenoxy)propane
Glycidyl 4-nitrophenyl ether
2-((4-nitrophenoxy)methyl)oxirane
Glycidyl p-nitrophenyl ether
Glycidylnitrophenyl ether
p-Nitrophenol glycidyl ether
1-(p-Nitrophenoxy)-2,3-epoxypropane
2,3-Epoxy-1-(p-nitrophenoxy)propane
p-Nitrophenylglycidyl ether
NSC 1733
Oxirane, [(4-nitrophenoxy)methyl]-
CCRIS 6429
((p-Nitrophenoxy)methyl)oxirane
((4-NITROPHENOXY)METHYL)OXIRANE
Propane, 1,2-epoxy-3-(p-nitrophenoxy)-
EINECS 226-057-3
Oxirane, ((4-nitrophenoxy)methyl)-
1,2-Epoxy-3(p-nitrophenoxy)-propane
CHEBI:508
NSC-1733
UNII-96071991U0
Oxirane, 2-((4-nitrophenoxy)methyl)-
Oxirane, 2-[(4-nitrophenoxy)methyl]-
4-nitrophenyl glycidyl ether
[(p-nitrophenoxy)methyl]oxirane
DTXSID60863512
96071991U0
DTXCID60214742
fpigobkndyaztp-uhfffaoysa-n
5255-75-4
EPNP
p-Nitrophenyl glycidyl ether
Nitrophenyl glycidyl ether
1,2-Epoxy-3-(4'-nitrophenoxy)propane
CHEMBL33775
Nitrophenyl glycidyl ether, p-
4-(2,3-Epoxypropoxy)nitrobenzene
MFCD00041845
SCHEMBL517975
NSC1733
2-(4-nitrophenoxymethyl)-oxirane
2-(4-nitro-phenoxymethyl)-oxirane
4-(2,3-epoxypropoxy) nitrobenzene
2-[(4-nitrophenoxy)methyl]-oxirane
BDBM50284985
STL582583
2-[(4-Nitrophenoxy)methyl]oxirane #
AKOS000149480
AKOS016843596
Propane,2-epoxy-3-(p-nitrophenoxy)-
1-(4-Nitrophenoxy)-2,3-epoxypropane
3-(4-nitrophenyloxy)-1,2-epoxypropane
1,2-Epoxy-3-(P-Nitrophenoxy)-Propane
1,2-Epoxy-3-(4''-nitrophenoxy)propane
FE152760
PD195113
PS-10361
4-(2,3-EPOXYPROPOXY)-NITROBENZENE
DB-025534
DB-339601
CS-0205886
NS00044123
C04274
G77588
Q27105305
125228-75-3