2,3-Diphenyloxirane
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- Molecular formula
- C14H12O
- CAS Number
- 3885-53-0
- IUPAC Name
- 2,3-diphenyloxirane
- Molecular Weight
- 196.25g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.1795g/cm3
- Synonyms
- Stilbene oxide
Identification
Interesting facts
Interesting Facts about 2,3-Diphenyloxirane
2,3-Diphenyloxirane is a fascinating compound that belongs to the family of epoxides, known for their unique three-membered cyclic ether structure. This compound is of particular interest in organic chemistry due to its potential applications and reactivity.
Key Features and Applications
- Reactivity: The oxirane ring in 2,3-diphenyloxirane is highly reactive, making it an excellent substrate for ring-opening reactions. This feature allows chemists to introduce a variety of functional groups, thus broadening its application scope.
- Synthetic Applications: It serves as an important intermediate in the synthesis of pharmaceuticals and agrochemicals, highlighting its utility in industrial chemistry.
- Chiral Synthesis: The compound can be used in asymmetric synthesis, which is crucial for developing chiral molecules in drug design.
Significance in Research
Researchers have noted several interesting aspects of this compound:
- Mechanistic Studies: The unique structure of 2,3-diphenyloxirane allows for investigations into reaction mechanisms, especially those involving electrophilic and nucleophilic additions.
- Material Science: Epoxides, including 2,3-diphenyloxirane, are studied for their properties in polymers and coatings, contributing to advancements in material science.
- Biological Activity: Initial studies suggest potential biological activity, which warrants further exploration into the compound’s pharmacological properties.
As you delve deeper into organic synthesis and mechanistic studies, 2,3-diphenyloxirane exemplifies the rich intersection of chemistry and its practical applications. Its diverse reactivity and relevance in both synthetic pathways and material science underscore its importance in the field.