Glycidyl 4-nitrophenyl ether

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Identification

Molecular formula
C9H9NO4
CAS Number
13349-82-1
IUPAC Name
2-[(4-nitrophenoxy)methyl]oxirane
Molecular Weight
195.18g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.2920g/cm3
Synonyms
1, 2-epoxy-3-(4-nitrophenoxy)propane
Interesting facts

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

2-[(4-nitrophenoxy)methyl]oxirane is a fascinating compound that demonstrates the intricate relationship between structure and function in organic chemistry. As a member of the epoxide family, this compound features a three-membered cyclic ether that is characterized by unique reactivity patterns. Below are some compelling insights into this compound:

  • Functional Groups: The presence of both the nitro group and the epoxide functionality makes this compound particularly interesting, as the nitro group can influence the reactivity and polarity of the molecule.
  • Reactivity: The epoxide group is strained and highly reactive, making it an excellent candidate for various chemical reactions, including nucleophilic attack which can lead to the formation of more complex structures.
  • Applications: Compounds like 2-[(4-nitrophenoxy)methyl]oxirane are often used in the synthesis of polymers, pharmaceuticals, and agrochemicals, showcasing their versatility in multiple fields.
  • Biodegradability: Some epoxides have been studied for their potential environmental impact, as they can undergo hydrolysis, which may lead to less harmful products in aquatic systems.
  • Structure-Activity Relationship (SAR): The incorporation of the nitrophenoxy moiety is of particular interest for medicinal chemistry, as variations in substituent groups can profoundly affect biological activity.

In conclusion, 2-[(4-nitrophenoxy)methyl]oxirane not only embodies the principles of organic reactivity but also highlights the significance of modifying chemical structures for improved functionality. As scientists continue to explore its properties, this compound serves as a reminder of the creative potential within chemical research.

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