Details
Stereochemistry | ACHIRAL |
Molecular Formula | C9H8O2 |
Molecular Weight | 148.1586 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
CC(=O)C(=O)C1=CC=CC=C1
InChI
InChIKey=BVQVLAIMHVDZEL-UHFFFAOYSA-N
InChI=1S/C9H8O2/c1-7(10)9(11)8-5-3-2-4-6-8/h2-6H,1H3
Approval Year
PubMed
Title | Date | PubMed |
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Influence of photoinitiator type on the rate of polymerization, degree of conversion, hardness and yellowing of dental resin composites. | 2008 Sep |
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A combined NMR, DFT, and X-ray investigation of some cinchona alkaloid O-ethers. | 2008 Sep 5 |
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Effect of co-initiator ratio on the polymer properties of experimental resin composites formulated with camphorquinone and phenyl-propanedione. | 2009 Mar |
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Characterization of a rat NADPH-dependent aldo-keto reductase (AKR1B13) induced by oxidative stress. | 2009 Mar 16 |
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Effect of different photo-initiators and light curing units on degree of conversion of composites. | 2010 Jul-Sep |
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Chiral Pt/ZrO2 catalysts. Enantioselective hydrogenation of 1-phenyl-1,2-propanedione. | 2010 May 12 |
Patents
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Classification Tree | Code System | Code | ||
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JECFA EVALUATION |
1-PHENYL-1,2-PROPANEDIONE
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834
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63552
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DTXSID3060372
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209-435-2
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ZB5XA3GD0I
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7643
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579-07-7
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11363
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SUBSTANCE RECORD