1-PHENYL-1,2-PROPANEDIONE

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

Structure Search

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

HIDE SMILES / InChI

Molecular Formula	C9H8O2
Molecular Weight	148.1586
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

PubMed

Title	Date	PubMed
In vitro photosensitization initiated by camphorquinone and phenyl propanedione in dental polymeric materials.	2010-09-02	20576444
A new in vitro method for identifying chemical sensitizers combining peptide binding with ARE/EpRE-mediated gene expression in human skin cells.	2010-09	20491607
Characterization of two aldo-keto reductases from Gluconobacter oxydans 621H capable of regio- and stereoselective alpha-ketocarbonyl reduction.	2010-07	20414648
Composition and stereochemistry of ephedrine alkaloids accumulation in Ephedra sinica Stapf.	2010-06	20417943
Chiral Pt/ZrO2 catalysts. Enantioselective hydrogenation of 1-phenyl-1,2-propanedione.	2010-05-12	20657492
Effect of different photo-initiators and light curing units on degree of conversion of composites.	2010-03-17	20877961
Effect of various visible light photoinitiators on the polymerization and color of light-activated resins.	2009-07	19721283
Alternative photoinitiator system reduces the rate of stress development without compromising the final properties of the dental composite.	2009-05	19111334
Experimental and theoretical analysis of asymmetric induction in heterogeneous catalysis: diastereoselective hydrogenation of chiral alpha-hydroxyketones over Pt catalyst.	2009-04-01	19260682
Characterization of a rat NADPH-dependent aldo-keto reductase (AKR1B13) induced by oxidative stress.	2009-03-16	18845131
Effect of co-initiator ratio on the polymer properties of experimental resin composites formulated with camphorquinone and phenyl-propanedione.	2009-03	18848352
A combined NMR, DFT, and X-ray investigation of some cinchona alkaloid O-ethers.	2008-09-05	18683975
Influence of photoinitiator type on the rate of polymerization, degree of conversion, hardness and yellowing of dental resin composites.	2008-09	18325583
Direct determination of ephedrine intermediate in a biotransformation reaction using infrared spectroscopy and PLS.	2008-05-30	18585178
Photopolymerization of N,N-dimethylaminobenzyl alcohol as amine co-initiator for light-cured dental resins.	2008-05	17804051
Developmental patterns of phenylpropylamino alkaloids accumulation in khat (Catha edulis, Forsk.).	2007-12-03	17928181
Photoinitiation chemistry affects light transmission and degree of conversion of curing experimental dental resin composites.	2007-07	16914191
The initiating radical yields and the efficiency of polymerization for various dental photoinitiators excited by different light curing units.	2006-06	16289725
Hep27, a member of the short-chain dehydrogenase/reductase family, is an NADPH-dependent dicarbonyl reductase expressed in vascular endothelial tissue.	2006-05	16685466
Effect of ultrasound in enantioselective hydrogenation of 1-phenyl-1,2-propanedione: comparison of catalyst activation, solvents and supports.	2006-01	16223690
Conformational flexibility, UV-induced decarbonylation, and FTIR spectra of 1-phenyl-1,2 propanedione in solid xenon and in the low temperature amorphous phase.	2005-06-30	16833887
Molecular probe for a fluorous medium: long-lived phosphorescence of alpha-diketones in perfluoromethylcyclohexane at room temperature.	2005-03	15790117
Influence of light-curing procedures and photo-initiator/co-initiator composition on the degree of conversion of light-curing resins.	2005-01	15754143
Utilisation of on-line acoustic irradiation as a means to counter-effect catalyst deactivation in heterogeneous catalysis.	2004-05	15081987
Novel laser-induced luminescence resulting from benzophenone/O-propylated p-tert-butylcalix[4]arene complexes. A diffuse reflectance study.	2003-10	14606755
Microbial degradation of illicit drugs, their precursors, and manufacturing by-products: implications for clandestine drug laboratory investigation and environmental assessment.	2003-06-24	12842360
Influence of composition on rate of polymerization contraction of light-curing resin composites.	2002-06	12166907
Intercalation of multiple carbon atoms between the carbonyls of alpha-diketones.	2001-10-05	11578223
SPME/GC-MS characterization of volatiles associated with methamphetamine: toward the development of a pseudomethamphetamine training material.	2001-09	11569539

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 20:15:29 GMT 2025` Edited by `admin` on `Mon Mar 31 20:15:29 GMT 2025`
Record UNII	ZB5XA3GD0I
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

1-PHENYL-1,2-PROPANEDIONE

Systematic Name

English

FEMA NO. 3226

Preferred Name

English

ACETYLBENZOYL

Common Name

English

1-PHENYL-2-OXOPROPAN-1-ONE

Systematic Name

English

3-PHENYL-2,3-PROPANEDIONE

Systematic Name

English

PYRUVOPHENONE

Systematic Name

English

METHYLPHENYLGLYOXAL

Systematic Name

English

1,2-PROPANEDIONE, 1-PHENYL-

Systematic Name

English

BENZOYL METHYL KETONE

Systematic Name

English

BENZOYLACETYL

Common Name

English

2-OXOPROPIOPHENONE

Systematic Name

English

1-PHENYL-1,2-PROPANEDIONE [FHFI]

Common Name

English

NSC-7643

Code

English

Classification Tree Code System Code

JECFA EVALUATION

1-PHENYL-1,2-PROPANEDIONE