Glycidyl 2-methylphenyl ether
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- Molecular formula
- C10H12O2
- CAS Number
- 2210-74-4
- IUPAC Name
- 2-[(2-methylphenoxy)methyl]oxirane
- Molecular Weight
- 164.20g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.0620g/cm3
- Synonyms
- 2210-79-9
Identification
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.