579-07-7 | 1-Phenyl-1,2-propanedione

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$15.00	$10.00
10g	98%	in stock	$26.00	$18.00
25g	98%	in stock	$49.00	$34.00
100g	98%	in stock	$145.00	$102.00
500g	98%	in stock	$518.00	$362.00

Description

• Catalog Number: AB54096
• Chemical Name: 1-Phenyl-1,2-propanedione
• CAS Number: 579-07-7
• Molecular Formula: C9H8O2
• Molecular Weight: 148.1586
• MDL Number: MFCD00008755
• SMILES: O=C(c1ccccc1)C(=O)C
• NSC Number: 7643

Computed Properties

• Complexity: 166
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• XLogP3: 1.7

Literature

• Benzaldehyde is a precursor of phenylpropylamino alkaloids as revealed by targeted metabolic profiling and comparative biochemical analyses in Ephedra spp.

  Phytochemistry 20120901

• Photo-crosslinkable cyanoacrylate bioadhesive: shrinkage kinetics, dynamic mechanical properties, and biocompatibility of adhesives containing TMPTMA and POSS nanostructures as crosslinking agents.

  Journal of biomedical materials research. Part A 20111101

• Requirements for mammalian carboxylesterase inhibition by substituted ethane-1,2-diones.

  Bioorganic & medicinal chemistry 20110801

• Can phenyl-propanedione influence Knoop hardness, rate of polymerization and bond strength of resin composite restorations?

  Journal of dentistry 20110601

• Light-curing of dental resins with GaN violet laser diode: the effect of photoinitiator on mechanical strength.

  Lasers in medical science 20110501

• Expressed sequence tag analysis of khat (Catha edulis) provides a putative molecular biochemical basis for the biosynthesis of phenylpropylamino alkaloids.

  Genetics and molecular biology 20110101

• In vitro photosensitization initiated by camphorquinone and phenyl propanedione in dental polymeric materials.

  Journal of photochemistry and photobiology. B, Biology 20100902

• A new in vitro method for identifying chemical sensitizers combining peptide binding with ARE/EpRE-mediated gene expression in human skin cells.

  Cutaneous and ocular toxicology 20100901

• Characterization of two aldo-keto reductases from Gluconobacter oxydans 621H capable of regio- and stereoselective alpha-ketocarbonyl reduction.

  Applied microbiology and biotechnology 20100701

• Composition and stereochemistry of ephedrine alkaloids accumulation in Ephedra sinica Stapf.

  Phytochemistry 20100601

• Chiral Pt/ZrO2 catalysts. Enantioselective hydrogenation of 1-phenyl-1,2-propanedione.

  Molecules (Basel, Switzerland) 20100512

• Effect of different photo-initiators and light curing units on degree of conversion of composites.

  Brazilian oral research 20100101

• Effect of various visible light photoinitiators on the polymerization and color of light-activated resins.

  Dental materials journal 20090701

• Alternative photoinitiator system reduces the rate of stress development without compromising the final properties of the dental composite.

  Dental materials : official publication of the Academy of Dental Materials 20090501

• Experimental and theoretical analysis of asymmetric induction in heterogeneous catalysis: diastereoselective hydrogenation of chiral alpha-hydroxyketones over Pt catalyst.

  Journal of the American Chemical Society 20090401

• Characterization of a rat NADPH-dependent aldo-keto reductase (AKR1B13) induced by oxidative stress.

  Chemico-biological interactions 20090316

• Effect of co-initiator ratio on the polymer properties of experimental resin composites formulated with camphorquinone and phenyl-propanedione.

  Dental materials : official publication of the Academy of Dental Materials 20090301

• A combined NMR, DFT, and X-ray investigation of some cinchona alkaloid O-ethers.

  The Journal of organic chemistry 20080905

• Influence of photoinitiator type on the rate of polymerization, degree of conversion, hardness and yellowing of dental resin composites.

  Dental materials : official publication of the Academy of Dental Materials 20080901

• Direct determination of ephedrine intermediate in a biotransformation reaction using infrared spectroscopy and PLS.

  Talanta 20080530

• Photopolymerization of N,N-dimethylaminobenzyl alcohol as amine co-initiator for light-cured dental resins.

  Dental materials : official publication of the Academy of Dental Materials 20080501

• Developmental patterns of phenylpropylamino alkaloids accumulation in khat (Catha edulis, Forsk.).

  Journal of ethnopharmacology 20071203

• Photoinitiation chemistry affects light transmission and degree of conversion of curing experimental dental resin composites.

  Dental materials : official publication of the Academy of Dental Materials 20070701

• The initiating radical yields and the efficiency of polymerization for various dental photoinitiators excited by different light curing units.

  Dental materials : official publication of the Academy of Dental Materials 20060601

• Hep27, a member of the short-chain dehydrogenase/reductase family, is an NADPH-dependent dicarbonyl reductase expressed in vascular endothelial tissue.

  Cellular and molecular life sciences : CMLS 20060501

• Effect of ultrasound in enantioselective hydrogenation of 1-phenyl-1,2-propanedione: comparison of catalyst activation, solvents and supports.

  Ultrasonics sonochemistry 20060101

• Conformational flexibility, UV-induced decarbonylation, and FTIR spectra of 1-phenyl-1,2 propanedione in solid xenon and in the low temperature amorphous phase.

  The journal of physical chemistry. A 20050630

• Identification and characterization of novel benzil (diphenylethane-1,2-dione) analogues as inhibitors of mammalian carboxylesterases.

  Journal of medicinal chemistry 20050421

• Molecular probe for a fluorous medium: long-lived phosphorescence of alpha-diketones in perfluoromethylcyclohexane at room temperature.

  Analytical sciences : the international journal of the Japan Society for Analytical Chemistry 20050301

• Influence of light-curing procedures and photo-initiator/co-initiator composition on the degree of conversion of light-curing resins.

  Journal of materials science. Materials in medicine 20050101

• Utilisation of on-line acoustic irradiation as a means to counter-effect catalyst deactivation in heterogeneous catalysis.

  Ultrasonics sonochemistry 20040501

• Novel laser-induced luminescence resulting from benzophenone/O-propylated p-tert-butylcalix[4]arene complexes. A diffuse reflectance study.

  Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology 20031001

• Microbial degradation of illicit drugs, their precursors, and manufacturing by-products: implications for clandestine drug laboratory investigation and environmental assessment.

  Forensic science international 20030624

• Influence of composition on rate of polymerization contraction of light-curing resin composites.

  Acta odontologica Scandinavica 20020601

• Intercalation of multiple carbon atoms between the carbonyls of alpha-diketones.

  The Journal of organic chemistry 20011005

• SPME/GC-MS characterization of volatiles associated with methamphetamine: toward the development of a pseudomethamphetamine training material.

  Journal of forensic sciences 20010901