| Weight | 210.276 g/mol |
|---|---|
| Formula | C15H14O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 2 |
| Rotatable Bonds | 4 |
1,3-Diphenylacetone (102-04-5)
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- Reactions of 3-acylchromones with dimethyl 1,3-acetonedicarboxylate and 1,3-diphenylacetone: one-pot synthesis of functionalized 2-hydroxybenzophenones, 6H-benzo[c]chromenes and benzo[c]coumarins (Organic and Biomolecular Chemistry, 2012)
- A study on the doubleMannich reaction with 1,3-diphenylacetone (Monatshefte Fur Chemie, 1984)
- Cooperative effect of surface sites on the laser flash photolysis of 1,1-diphenylacetone and1,1,3,3-tetraphenylacetone adsorbed on layered clays. Generation of radicals and carbocations (The Journal of Physical Chemistry, 1994)
- (S,S)1,3Bis[(2methoxyethoxy)methoxy]1,3diphenylacetone A New Chiral Ketone with C2 Symmetry (Chemische Berichte, 1989)
- Analysis of the infrared and Raman spectra of the symmetrically substituted 1,3-diphenylurea and 1,3-diphenylacetone (dibenzyl ketone). (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2012)
- Convenient Laboratory Method forthe Synthesis of Symmetrical 1,3-Diphenylacetone Derivatives (Synthesis, 2011)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)CC(=O)CC2=CC=CC=C2
-
InChIKeyYFKBXYGUSOXJGS-UHFFFAOYSA-N
- Pubchem - 1,3-Diphenylacetone
- Wikipedia - 1,3-diphenyl-2-propanone
Dibenzyl ketone, or 1,3-diphenylacetone, is an organic compound composed of two benzyl groups attached to a central carbonyl group. This results in the central carbonyl carbon atom being electrophilic and the two adjacent carbon atoms slightly nucleophilic. For this reason, dibenzyl ketone is frequently used in an aldol condensation reaction with benzil (a dicarbonyl) and base to create tetraphenylcyclopentadienone.
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1,3-Diphenylacetone
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