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Glycidyl 4-methoxyphenyl ether

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Identification
Molecular formula
C10H12O3
CAS number
56718-71-9
IUPAC name
2-[(4-methoxyphenoxy)methyl]oxirane
State
State

At room temperature, Glycidyl 4-methoxyphenyl ether is typically a liquid. Its low melting point allows it to remain in liquid form under most typical laboratory conditions.

Melting point (Celsius)
-44.00
Melting point (Kelvin)
229.15
Boiling point (Celsius)
275.00
Boiling point (Kelvin)
548.15
General information
Molecular weight
180.20g/mol
Molar mass
180.2010g/mol
Density
1.1160g/cm3
Appearence

Glycidyl 4-methoxyphenyl ether appears as a colorless to pale yellow liquid. It is often characterized by its clear appearance and its tendency to become more viscous as temperature decreases.

Comment on solubility

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

2-[(4-methoxyphenoxy)methyl]oxirane, a complex organic compound, exhibits intriguing solubility characteristics that are influenced by its molecular structure. The presence of both an oxirane ring and a methoxyphenoxy group contributes to its behavior in different solvents. Here are some key points regarding its solubility:

  • Solvent Affinity: This compound typically shows better solubility in organic solvents rather than in water, owing to its non-polar characteristics brought about by the aromatic methoxy group.
  • Hydrophilic and Hydrophobic Balance: The dual nature of the structure, with both hydrophobic (aromatic) and potentially hydrophilic (ether) sections, can lead to variable solubility in mixed solvent systems.
  • Temperature Influence: Like many organic compounds, the solubility of 2-[(4-methoxyphenoxy)methyl]oxirane may increase with temperature, helping it dissolve more readily in chosen solvents.
  • Interactions with Solvents: The solubility can also be significantly affected by hydrogen bonding and van der Waals forces in various solvent environments.

In conclusion, while 2-[(4-methoxyphenoxy)methyl]oxirane may not be highly soluble in polar solvents like water, its solubility in non-polar or organic solvents makes it a compound of interest, especially for applications requiring organic reactions. Understanding these solubility behaviors is crucial for practical applications in chemical synthesis and product formulation.

Interesting facts

Interesting Facts About 2-[(4-methoxyphenoxy)methyl]oxirane

2-[(4-methoxyphenoxy)methyl]oxirane, commonly known as a glycidyl ether, is a versatile compound with several noteworthy characteristics that intrigue both chemists and students alike.

Key Highlights:

  • Structure and Reactivity: 2-[(4-methoxyphenoxy)methyl]oxirane contains an epoxide functional group, which is known for its high reactivity. This property makes the compound a valuable intermediate in organic synthesis, opening pathways for creating various derivatives.
  • Applications: Due to its unique chemical structure, this compound finds applications in several fields, such as:
    • Polymer chemistry - It can act as a building block for epoxy resins.
    • Pharmaceuticals - Its reactive nature allows for the modification of drug molecules, potentially improving efficacy.
    • Material science - Used in formulations requiring surface coatings or adhesives.
  • Toxicology and Safety: Precautions are necessary when handling this compound, as with many epoxides, due to potential health hazards like skin irritation. Proper laboratory practices are essential for safety.
  • Synthetic Pathways: 2-[(4-methoxyphenoxy)methyl]oxirane can be synthesized through various methods, typically involving the reaction of phenolic compounds with epichlorohydrin. Understanding these pathways is crucial for chemists looking to innovate in synthetic methods.

Conclusion

With its reactivity and applicability across multiple scientific domains, 2-[(4-methoxyphenoxy)methyl]oxirane serves as an excellent example of how a single compound can bridge different aspects of chemistry. As we continue to explore its properties and uses, the possibilities remain vast and promising.

Synonyms
2,3-Epoxypropyl 4'-methoxyphenyl ether
218-653-7
2211-94-1
2-[(4-Methoxyphenoxy)methyl]oxirane
Glycidyl 4-methoxyphenyl ether
2,3-Epoxypropyl-4-methoxyphenyl ether
2-((4-Methoxyphenoxy)methyl)oxirane
p-Methoxyphenyl glycidyl ether
Methoxyphenyl glycidyl ether
Glycidyl p-methoxyphenyl ether
2-(p-Methoxyphenoxymethyl)oxirane
((4-Methoxyphenoxy)methyl)oxirane
Anisole, p-(2,3-epoxypropoxy)-
Benzene, 1-(2,3-epoxypropoxy)-4-methoxy-
MFCD00005135
NSC 26796
2,3-Epoxypropyl p-methoxyphenyl ether
NSC 126709
Oxirane, [(4-methoxyphenoxy)methyl]-
NSC-26796
NSC-126709
Oxirane, ((4-methoxyphenoxy)methyl)-
2,3-Epoxypropyl para-methoxyphenyl ether
26744-15-0
[(4-methoxyphenoxy)methyl]oxirane
EINECS 218-653-7
2,3-Epoxypropyl 4-methoxyphenyl ether
BRN 0128888
4-methoxyphenoxymethyloxirane
JY25P7XTV5
SCHEMBL410250
4-methoxyphenyl glycidyl ether
2-(4-methoxyphenoxymethyl)oxirane
DTXSID201305536
NSC26796
NSC126709
STK802523
(+/-)-O-(4-Methoxyphenyl)glycidol
Glycidyl 4-methoxyphenyl ether, 99%
AKOS000122886
AKOS016037122
1,2-epoxy-3-(4-methoxyphenoxy)propane
1-(p-Methoxyphenoxy)-2,3-epoxypropane
2-[(4-Methoxyphenoxy)methyl]oxirane #
1-(4-Methoxyphenoxy)-2,3-epoxypropane
3-(4-Methoxyphenoxy)-1,2-epoxypropane
Oxirane, 2-[(4-methoxyphenoxy)methyl]-
SY078798
DB-045800
CS-0197032
NS00049584
EN300-22425
1,2-EPOXY-3-(P-METHOXYPHENOXY)PROPANE
6N-803
E78142
5-17-03-00025 (Beilstein Handbook Reference)
Z147642770