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Glycidyl 2-methylphenyl ether

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

Liquid at room temperature.

Melting point (Celsius)
-24.00
Melting point (Kelvin)
249.15
Boiling point (Celsius)
252.00
Boiling point (Kelvin)
525.15
General information
Molecular weight
164.20g/mol
Molar mass
164.2020g/mol
Density
1.0620g/cm3
Appearence

Glycidyl 2-methylphenyl ether is typically a colorless or pale yellow liquid.

Comment on solubility

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

The solubility of 2-[(2-methylphenoxy)methyl]oxirane (often referred to as a glycidyl ether) can be influenced by various factors, including its molecular structure and the presence of functional groups within the compound.

Typically, 2-[(2-methylphenoxy)methyl]oxirane is expected to demonstrate the following solubility characteristics:

  • Polar Solvents: It is likely to be more soluble in polar solvents (e.g., water, methanol) due to potential hydrogen bonding interactions.
  • Non-polar Solvents: In contrast, it may have limited solubility in non-polar solvents (like hexane), given its polar functional groups.
  • Temperature Dependency: As with many organic compounds, increased temperature can enhance solubility due to greater molecular movement.

In practical applications, determining the exact solubility of C10H12O2 may require empirical testing, as solubility is influenced by factors such as interactions with other substances and the degree of purity.

Always consider that "solubility can vary widely," and experimental measurements are often crucial in assessing the behavior of compounds in specific environments.

Interesting facts

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

2-[(2-methylphenoxy)methyl]oxirane, commonly known as a type of epoxide, is a fascinating compound that showcases the versatility of organic chemistry. Here are some notable aspects of this intriguing compound:

  • Epoxide Structure: The oxirane ring, a three-membered cyclic ether, is known for its strain due to the angle between its atoms. This makes epoxides highly reactive and thus very useful in various applications.
  • Synthetic Utility: One of the key uses of 2-[(2-methylphenoxy)methyl]oxirane is in the synthesis of more complex molecules, demonstrating its role as a valuable building block in organic synthesis.
  • Biological Activity: Compounds like this one often exhibit interesting biological activities, including antimicrobial and antifungal properties, which are a subject of research in pharmaceuticals.
  • Polymer Chemistry: This compound can also be utilized in the formulation of epoxy resins, which are used extensively in coatings, adhesives, and materials science. Its reactivity enables the formation of tough and durable networks.
  • Environmental Considerations: As with many synthetic compounds, understanding the ecological impact of 2-[(2-methylphenoxy)methyl]oxirane is crucial. Researchers are exploring ways to mitigate any potential negative effects associated with its use.

Through the lens of a chemist, 2-[(2-methylphenoxy)methyl]oxirane is not just another compound but a gateway to a wide array of applications and studies that enhance our understanding of organic and polymer chemistry. The significance of this compound extends from its fundamental chemical properties to practical applications in the production of high-performance materials.

Synonyms
2210-79-9
O-CRESYL GLYCIDYL ETHER
2-[(2-Methylphenoxy)methyl]oxirane
Araldite DY 023
2-((2-Methylphenoxy)methyl)oxirane
((2-Methylphenoxy)methyl)oxirane
Oxirane, [(2-methylphenoxy)methyl]-
DTXSID8024862
1,2-Epoxy-3-(o-tolyoxy)propane
Oxirane, ((2-methylphenoxy)methyl)-
Heloxy 62
CCRIS 2636
o-Tolyl glycidyl ether
o-Tolyl epoxypropyl ether
EINECS 218-645-3
NSC-11571
NSC-20291
8Z744RD471
Propane, 1,2-epoxy-3-(o-tolyoxy)-
Cresol, o-epoxypropyl ether
BRN 0004585
AI3-13110
DTXCID604862
UNII-8Z744RD471
3-(2-Methylphenoxy)-1,2-epoxypropane
EC 218-645-3
4-17-00-00993 (Beilstein Handbook Reference)
oKresolglycidaether
Glycidyl otolyl ether
oCresol glycidyl ether
OCresyl glycidyl ether
Glycidyl omethylphenyl ether
2Methylphenyl glycidyl ether
Glycidyl 2methylphenyl ether
1,2Epoxy3(otolyoxy)propane
EPODIL 742
1,2Epoxy3(otolyloxy)propane
2,3-Epoxypropyl-o-tolyl ether
Propane, 1,2epoxy3(otolyoxy)
((2Methylphenoxy)methyl)oxirane
Propane, 1,2epoxy3(otolyloxy)
1(oMethylphenoxy)2,3epoxypropane
2((2Methylphenoxy)methyl)oxirane
1(2Methylphenoxy)2,3epoxypropane
1,2Epoxy3(2methylphenoxy)propane
218-645-3
26447-14-3
kfusxmdyopxkkt-uhfffaoysa-n
Glycidyl 2-methylphenyl ether
2-((o-tolyloxy)methyl)oxirane
o-Cresol glycidyl ether
Glycidyl o-tolyl ether
1,2-Epoxy-3-(2-methylphenoxy)propane
1-(2-Methylphenoxy)-2,3-epoxypropane
o-Kresol-glycidaether
2-Methylphenyl glycidyl ether
1-(o-Methylphenoxy)-2,3-epoxypropane
1,2-Epoxy-3-(o-tolyloxy)propane
Glycidyl o-methylphenyl ether
Propane, 1,2-epoxy-3-(o-tolyloxy)-
2-(2-Methylphenoxymethyl)oxirane
NSC 11571
NSC 20291
Oxirane, 2-[(methylphenoxy)methyl]-
(2-Methylphenoxymethyl)oxirane
1-(2,3-Epoxypropoxy)-2-methylbenzene
WLN: T3OTJ B1OR B1
Propane,2-epoxy-3-(o-tolyoxy)-
Propane,2-epoxy-3-(o-tolyloxy)-
Oxirane, 2-((2-methylphenoxy)methyl)-
Oxirane, 2-[(2-methylphenoxy)methyl]-
0-Cresyl glycidyl ether
Cresyl glycidyl ether, o-
Oxirane,2-[(2-methylphenoxy)methyl]-
2,3-Epoxypropyl o-tolyl ether
o-Kresol-glycidaether [German]
o-cresylglycidyl ether
SCHEMBL179950
CHEMBL1445408
CAA21079
NSC11571
NSC20291
Tox21_200885
MFCD00037847
AKOS000200353
AKOS016874461
1-(2-methylphenoxy)2,3-epoxy-propane
1-(o-methyl-phenoxy)-2,3-epoxypropane
2,3-Epoxy-1-(2-methylphenoxy)propane
NCGC00091378-01
NCGC00091378-02
NCGC00258439-01
1-(o-methyl-phenoxy)-2,3-epoxy-propane
LS-13793
CAS-2210-79-9
DB-125812
CS-0204435
NS00006365
EN300-09422
N11750
A852251
Q1964115
Glycidyl 2-methylphenyl ether, technical grade, 90%
Z56346888
F1995-0400