Glycidyl ethyl ether

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Identification

Molecular formula
C5H10O2
CAS Number
3121-43-3
IUPAC Name
2-(ethoxymethyl)oxirane
Molecular Weight
102.13g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
0.9367g/cm3
Synonyms
ETHYL GLYCIDYL ETHER
Interesting facts

Interesting Facts About 2-(ethoxymethyl)oxirane

2-(ethoxymethyl)oxirane, commonly known as a type of epoxide, is a fascinating compound due to its unique structural and chemical properties. As a versatile intermediate in organic synthesis, it has garnered the interest of chemists and industry professionals alike. Here are some intriguing aspects of this compound:

  • Reactivity: Epoxides are known for their strain in the three-membered ring structure, making them highly reactive. This reactivity facilitates various chemical transformations, allowing chemists to create a wide range of derivatives.
  • Applications: 2-(ethoxymethyl)oxirane plays a crucial role in the synthesis of pharmaceuticals, agricultural chemicals, and polymers. Its utility in forming complex molecules makes it invaluable in many research and industrial settings.
  • Versatility: The ethoxy group contributes to the compound's solubility and enhances its reactivity with nucleophiles. This versatility paves the way for the preparation of diverse chemical products.
  • Synthesis: The synthesis of epoxides, including 2-(ethoxymethyl)oxirane, can be achieved through various methods, such as the oxidation of alkenes or the reaction of halohydrins. Understanding these pathways is essential for effective chemical manufacturing.
  • Safety Considerations: Like many reactive compounds, handling epoxides requires caution. They can be irritants and pose risks if not managed properly in laboratory settings.

As chemists continue to explore the significant potential of 2-(ethoxymethyl)oxirane, its role in advancing chemical research and development is expected to grow. Truly, this compound exemplifies the dynamic nature of organic chemistry!

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