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Epoxypropyl p-tolyl ether

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Identification
Molecular formula
C10H12O2
CAS number
2210-74-4
IUPAC name
2-[(4-methylphenoxy)methyl]oxirane
State
State

At room temperature, epoxypropyl p-tolyl ether is a liquid.

Melting point (Celsius)
-15.00
Melting point (Kelvin)
258.20
Boiling point (Celsius)
240.50
Boiling point (Kelvin)
513.70
General information
Molecular weight
164.20g/mol
Molar mass
164.2040g/mol
Density
1.0800g/cm3
Appearence

Epoxypropyl p-tolyl ether appears as a colorless to light yellow liquid. It has a slight, characteristic odor.

Comment on solubility

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

The solubility of 2-[(4-methylphenoxy)methyl]oxirane can be intriguing due to its unique structural features. This compound, which includes an epoxide ring and a phenoxy group, displays varying solubility characteristics depending on the solvent used.

Generally, the solubility behavior can be summarized as follows:

  • In Polar Solvents: The presence of the epoxide functional group suggests a tendency for 2-[(4-methylphenoxy)methyl]oxirane to dissolve in polar solvents, such as water and alcohols, due to hydrogen bonding capabilities.
  • In Non-Polar Solvents: The phenoxy group may enhance its solubility in non-polar solvents, as it can engage in van der Waals interactions.
  • Temperature Effects: Like many organic compounds, solubility can increase with temperature, making it crucial to consider temperature influences when assessing solubility.

In summary, while 2-[(4-methylphenoxy)methyl]oxirane is likely to exhibit variable solubility in different solvents, its specific solubility can only be determined through experimental data. As noted, "the context of solubility is key" for organic compounds, thus underscoring the importance of testing in various conditions.

Interesting facts

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

2-[(4-methylphenoxy)methyl]oxirane, often referred to as a type of epoxide, is a fascinating compound in organic chemistry due to its unique structure and reactivity. This compound features an oxirane (epoxide) ring that is an intriguing area of study for chemists focused on ring-opening reactions and the development of new synthetic pathways.

Key Characteristics:

  • Reactivity: The strained three-membered oxirane ring is highly reactive, making it a valuable building block in organic synthesis.
  • Applications in Synthesis: It serves as a precursor for various chemical reactions, including the creation of alcohols, amines, and carboxylic acids.
  • Biological Activity: Compounds with similar structures are often investigated for their potential pharmaceutical applications, such as anti-inflammatory and anticancer properties.

In addition, the presence of the 4-methylphenoxy group contributes to its chemical properties, influencing solubility and reactivity, which can be tailored for specific applications. As noted in various studies, "the integration of functional groups allows for greater versatility and innovation in compound design."
This flexibility makes 2-[(4-methylphenoxy)methyl]oxirane an exciting topic for research and exploration in both academic and industrial contexts.

Overall, the compound’s functional characteristics and potential applications underscore the importance of understanding chemical structures and their implications in various fields such as materials science, pharmaceuticals, and agrochemicals.

Synonyms
2186-24-5
CRESYL GLYCIDYL ETHER
2-[(4-Methylphenoxy)methyl]oxirane
p-Cresyl glycidyl ether
26447-14-3
p-Methylphenyl glycidyl ether
CCRIS 2637
EINECS 218-574-8
BRN 0117187
p-Methylphenol glycidyl ether
2,3-Epoxypropyl p-tolyl ether
DTXSID3024863
5-17-03-00016 (Beilstein Handbook Reference)
2-((4-Methylphenoxy)methyl)oxirane
Cresylglycide ether
Tolyl glycidyl ether
Cresol glycidal ether
Cresol glycidyl ether
Glycidyl methylphenyl ether
((Methylphenoxy)methyl)oxirane
HSDB 251
1,2-Epoxy-3-(tolyloxy)propane
EINECS 247-711-4
Propane, 1,2-epoxy-3-(tolyloxy)-
Glycidyl ptolyl ether
pCresol glycidyl ether
EPIOL C
GLYCIDYL TOLYL ETHER
pMethylphenyl glycidyl ether
HELEX 62
Glycidyl 4methylphenyl ether
EPODIL 472
1,2Epoxy3(ptolyloxy)propane
TOLYL EPOXYPROPYL ETHER
DTXCID004863
((4Methylphenoxy)methyl)oxirane
CRESOL, EPOXYPROPYL ETHER
DY 023
4-METHYLPHENOL, GLYCIDYL ETHER
((METHYLPHENOXY)METHYL)-OXIRANE
P-HYDROXYTOLUENE, GLYCIDYL ETHER
cufxmpwhowynso-uhfffaoysa-n
oxirane, ((methylphenoxy)methyl)-
oxirane, [(methylphenoxy)methyl]-
2-P-TOLYLOXYMETHYL-OXIRANE
2-((p-Tolyloxy)methyl)oxirane
Glycidyl p-tolyl ether
p-Cresol glycidyl ether
Glycidyl 4-methylphenyl ether
((4-Methylphenoxy)methyl)oxirane
1,2-Epoxy-3-(p-tolyloxy)propane
NSC 112255
Propane, 1,2-epoxy-3-(p-tolyloxy)-
1-p-(Tolyloxy)-2,3-epoxypropane
Oxirane, ((4-methylphenoxy)methyl)-
Oxirane, [(4-methylphenoxy)methyl]-
((p-Tolyloxy)methyl)oxirane
MFCD00046991
SCHEMBL187051
2,3-Epoxypropyl-p-tolyl ether
CHEMBL3249573
NSC112255
2-[(4-Methylphenoxy)methyl]-oxirane
AKOS000200286
AKOS016051063
AB02014
FC40360
NSC-112255
AS-10315
DB-046956
DB-066646
CS-0307861
NS00083710
EN300-09213
N12247
Z57046213