| Weight | 196.249 g/mol |
|---|---|
| Formula | C14H12O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 2 |
2,2-Diphenyloxirane (882-59-7)
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- Enantiodifferentiating cis-trans photoisomerizations of 1,2-diarylcyclopropanes and 2,3-diphenyloxirane sensitized by chiral aromatic esters (Journal of Organic Chemistry, 1993)
- Single route to chiral syn- and anti-2-amino-1,2-diphenylethanols via a new stereodivergent opening of trans-1,2-diphenyloxirane. (Journal of Organic Chemistry, 2003)
- Orbital Symmetry Control in the Photochemistry of trans-2,3-Diphenyloxirane. (Journal of Organic Chemistry, 1997)
- Reductive ring opening of cis- and trans-2,3-diphenyloxirane: a common intermediate (Tetrahedron, 2005)
- Medium Effects on Stereochemistry of Acid-Catalyzed Ethanolysis of trans-2,3-Diphenyloxirane (Bulletin of the Chemical Society of Japan, 1978)
- The oxidation potentials of cis- and trans-1,2-diphenylcyclopropane and cis- and trans-2,3-diphenyloxirane (Canadian Journal of Chemistry, 1979)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1C(O1)(C2=CC=CC=C2)C3=CC=CC=C3
-
InChIKeyPRLJMHVNHLTQJJ-UHFFFAOYSA-N
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Alternate Names
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Synthesis
benzene
+
Reactant
(Friedel-Crafts alkylation)
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