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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 of 1-PHENYL-1,2-PROPANEDIONE

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

Approval Year

PubMed

PubMed

TitleDatePubMed
Intercalation of multiple carbon atoms between the carbonyls of alpha-diketones.
2001 Oct 5
Influence of composition on rate of polymerization contraction of light-curing resin composites.
2002 Jun
Microbial degradation of illicit drugs, their precursors, and manufacturing by-products: implications for clandestine drug laboratory investigation and environmental assessment.
2003 Jun 24
Novel laser-induced luminescence resulting from benzophenone/O-propylated p-tert-butylcalix[4]arene complexes. A diffuse reflectance study.
2003 Oct
Utilisation of on-line acoustic irradiation as a means to counter-effect catalyst deactivation in heterogeneous catalysis.
2004 May
Influence of light-curing procedures and photo-initiator/co-initiator composition on the degree of conversion of light-curing resins.
2005 Jan
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 Jun 30
Molecular probe for a fluorous medium: long-lived phosphorescence of alpha-diketones in perfluoromethylcyclohexane at room temperature.
2005 Mar
Effect of ultrasound in enantioselective hydrogenation of 1-phenyl-1,2-propanedione: comparison of catalyst activation, solvents and supports.
2006 Jan
The initiating radical yields and the efficiency of polymerization for various dental photoinitiators excited by different light curing units.
2006 Jun
Hep27, a member of the short-chain dehydrogenase/reductase family, is an NADPH-dependent dicarbonyl reductase expressed in vascular endothelial tissue.
2006 May
Developmental patterns of phenylpropylamino alkaloids accumulation in khat (Catha edulis, Forsk.).
2007 Dec 3
Photopolymerization of N,N-dimethylaminobenzyl alcohol as amine co-initiator for light-cured dental resins.
2008 May
Direct determination of ephedrine intermediate in a biotransformation reaction using infrared spectroscopy and PLS.
2008 May 30
A combined NMR, DFT, and X-ray investigation of some cinchona alkaloid O-ethers.
2008 Sep 5
Effect of various visible light photoinitiators on the polymerization and color of light-activated resins.
2009 Jul
Alternative photoinitiator system reduces the rate of stress development without compromising the final properties of the dental composite.
2009 May
Composition and stereochemistry of ephedrine alkaloids accumulation in Ephedra sinica Stapf.
2010 Jun
A new in vitro method for identifying chemical sensitizers combining peptide binding with ARE/EpRE-mediated gene expression in human skin cells.
2010 Sep
In vitro photosensitization initiated by camphorquinone and phenyl propanedione in dental polymeric materials.
2010 Sep 2
Patents

Patents

Name Type Language
1-PHENYL-1,2-PROPANEDIONE
FHFI  
Systematic 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
FEMA NO. 3226
Code 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
Created by admin on Fri Dec 15 20:55:11 GMT 2023 , Edited by admin on Fri Dec 15 20:55:11 GMT 2023
Code System Code Type Description
JECFA MONOGRAPH
834
Created by admin on Fri Dec 15 20:55:11 GMT 2023 , Edited by admin on Fri Dec 15 20:55:11 GMT 2023
PRIMARY
CHEBI
63552
Created by admin on Fri Dec 15 20:55:11 GMT 2023 , Edited by admin on Fri Dec 15 20:55:11 GMT 2023
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EPA CompTox
DTXSID3060372
Created by admin on Fri Dec 15 20:55:11 GMT 2023 , Edited by admin on Fri Dec 15 20:55:11 GMT 2023
PRIMARY
ECHA (EC/EINECS)
209-435-2
Created by admin on Fri Dec 15 20:55:11 GMT 2023 , Edited by admin on Fri Dec 15 20:55:11 GMT 2023
PRIMARY
FDA UNII
ZB5XA3GD0I
Created by admin on Fri Dec 15 20:55:11 GMT 2023 , Edited by admin on Fri Dec 15 20:55:11 GMT 2023
PRIMARY
NSC
7643
Created by admin on Fri Dec 15 20:55:11 GMT 2023 , Edited by admin on Fri Dec 15 20:55:11 GMT 2023
PRIMARY
CAS
579-07-7
Created by admin on Fri Dec 15 20:55:11 GMT 2023 , Edited by admin on Fri Dec 15 20:55:11 GMT 2023
PRIMARY
PUBCHEM
11363
Created by admin on Fri Dec 15 20:55:11 GMT 2023 , Edited by admin on Fri Dec 15 20:55:11 GMT 2023
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