D33454
1,3-Diphenyl-1,3-propanedione
98%
Sinónimos:
Dibenzoylmethane
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Fórmula lineal:
(C6H5CO)2CH2
Número CAS:
Peso molecular:
224.25
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-398-9
Beilstein/REAXYS Number:
514910
MDL number:
Assay:
98%
Form:
crystals
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Permítanos ayudarleNombre del producto
1,3-Diphenyl-1,3-propanedione, 98%
InChI key
NZZIMKJIVMHWJC-UHFFFAOYSA-N
InChI
1S/C15H12O2/c16-14(12-7-3-1-4-8-12)11-15(17)13-9-5-2-6-10-13/h1-10H,11H2
SMILES string
O=C(CC(=O)c1ccccc1)c2ccccc2
assay
98%
form
crystals
bp
219-221 °C/18 mmHg (lit.)
mp
77-79 °C (lit.)
Quality Level
Gene Information
human ... ACHE(43), BCHE(590), CES1(1066)
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Categorías relacionadas
Application
- A radical-anion chain mechanism following dissociative electron transfer reduction of the model prostaglandin endoperoxide, 1,4-diphenyl-2,3-dioxabicyclo[2.2.1]heptane.: This study explores the unique chemical properties of 1,3-Diphenyl-1,3-propanedione in the context of electron transfer reactions. The research unveils its potential in creating advanced prostaglandin models, crucial for pharmaceutical applications and drug synthesis. This application is especially significant in the context of prostaglandin biosynthesis, offering a pathway to new drug development strategies within the pharmaceutical industry and biochemical research (Magri & Workentin, 2008).
General description
1,3-Diphenyl-1,3-propanedione also known as Dibenzoylmethane, a symmetrical ß-diketone with the ability to form strong intra and intermolecular hydrogen bonds is commonly used to produces a Schiff base in reaction with benzidine.
Clase de almacenamiento
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Zhaogang Nie et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 72(3), 554-560 (2008-12-17)
Rare-earth complex Sm(DBM)(3)Phen-doped poly(methyl methacrylate) was synthesized and its absorption and luminescence spectra were studied. The relationship between the coordinate environment of rare-earth ions and the Judd-Ofelt intensity parameter Omega(2) was analyzed and the spectroscopic quality factor, Omega(4)/Omega(6), for this
Mojtaba Shamsipur et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 77(1), 319-323 (2010-07-17)
A highly sensitive ion-selective bulk optode membrane for sensing UO2(2+) ion based on plasticized poly(vinyl chloride) containing 6,7,9,10,12,13,15,16,23,24,25,26-dodecahydrodibenzo[n,v][1,4,7,10,13,17,20]pentaoxa-diazacyclotricosine-22,27-dione as ionophore, dibenzodylmethane as chromoionophore and sodium tetraphenylborate as an ionic additive was prepared. In addition to its high stability, reproducibility and
Ka Lung Cheung et al.
Carcinogenesis, 31(5), 880-885 (2009-12-05)
Previously, phenethyl isothiocyanate (PEITC) and dibenzoylmethane (DBM) had been shown to inhibit intestinal carcinogenesis in Apc(Min/+) mice. In this study, we investigated the chemopreventive efficacy of PEITC and DBM in the azoxymethane (AOM)-initiated and dextran sodium sulfate (DSS)-promoted colon cancer
Yuichi Masuda et al.
The journal of physical chemistry. A, 116(18), 4485-4494 (2012-04-19)
Despite the importance of ultrafast (time scale exceeding 10(-11) s) intramolecular proton transfer (PT) events between electronic ground states in solution, experimental determination of the rates of such reactions has not yet been accomplished because of the limitations of the
Brooks M Hybertson et al.
Antioxidants (Basel, Switzerland), 8(5) (2019-05-07)
Bioactive phytochemicals in Rosmarinus officinalis, Withania somnifera, and Sophora japonica have a long history of human use to promote health. In this study we examined the cellular effects of a combination of extracts from these plant sources based on specified
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