Skip to main content

2,3-Diphenyloxirane

ADVERTISEMENT
Identification
Molecular formula
C14H12O
CAS number
3885-53-0
IUPAC name
2,3-diphenyloxirane
State
State

At room temperature, 2,3-diphenyloxirane is typically a liquid.

Melting point (Celsius)
46.00
Melting point (Kelvin)
319.15
Boiling point (Celsius)
297.00
Boiling point (Kelvin)
570.15
General information
Molecular weight
196.25g/mol
Molar mass
196.2470g/mol
Density
1.1795g/cm3
Appearence

2,3-Diphenyloxirane appears as a colorless to pale yellow liquid. It is an aromatic epoxide characterized by its oxirane (epoxide) ring, which is linked to two phenyl groups.

Comment on solubility

Solubility of 2,3-Diphenyloxirane

The solubility of 2,3-diphenyloxirane can be particularly intriguing due to its unique structure and the presence of multiple aromatic rings. Generally, the solubility of organic compounds, such as this one, is influenced by several factors, including polarity, molecular weight, and the ability to form hydrogen bonds.

Here are some key considerations regarding the solubility of 2,3-diphenyloxirane:

  • Polarity: 2,3-diphenyloxirane is a relatively non-polar compound, which often leads to low solubility in polar solvents, such as water.
  • Solvent Compatibility: It tends to dissolve better in non-polar or slightly polar solvents like ethanol, ether, or benzene.
  • Temperature Effects: Higher temperatures may increase solubility in certain solvents due to enhanced molecular motion.

To sum it up, while 2,3-diphenyloxirane demonstrates limited solubility in polar solvents, it is much more soluble in non-polar environments. This property is essential for applications where solvent choice is crucial for effective use of the compound.

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.

Synonyms
Stilbene oxide
17619-97-5
Oxirane, 2,3-diphenyl-
L47V7XQ2XK
CHEBI:50006
NSC-155516
2,3-DIPHENYLOXIRANE
1,2-Diphenylethyleneoxide
2,3-DIPHENYL-OXIRANE
Bibenzyl, .alpha.,.alpha.'-epoxy-
MFCD00066627
UNII-L47V7XQ2XK
MFCD00064311
Oxirane, 2,3-diphenyl- (9CI)
Oxirane,3-diphenyl-
NSC 155516
2,3-Diphenyloxirane #
Bibenzyl,.alpha.'-epoxy-
NCIOpen2_001945
Oxirane,3-diphenyl-, cis-
SCHEMBL63809
ghl.PD_Mitscher_leg0.611
Bibenzyl, alpha,alpha'-epoxy-
SCHEMBL4058416
DTXSID20937561
Bibenzyl,.alpha.'-epoxy-, cis-
NSC133513
NSC155516
AKOS000167808
LS-14277
PD193349
Bibenzyl, .alpha.,.alpha.'-epoxy-, cis-
DB-288337
NS00044681
H39587
AD-266/40316974
Q27121647