D33454
1,3-Diphenyl-1,3-propanedione
98%
Synonyme(s) :
Dibenzoylmethane
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About This Item
Formule linéaire :
(C6H5CO)2CH2
Numéro CAS:
Poids moléculaire :
224.25
Numéro Beilstein :
514910
Numéro CE :
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22
Produits recommandés
Niveau de qualité
Pureté
98%
Forme
crystals
Point d'ébullition
219-221 °C/18 mmHg (lit.)
Pf
77-79 °C (lit.)
Chaîne SMILES
O=C(CC(=O)c1ccccc1)c2ccccc2
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
Clé InChI
NZZIMKJIVMHWJC-UHFFFAOYSA-N
Informations sur le gène
human ... ACHE(43) , BCHE(590) , CES1(1066)
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Description générale
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.
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).
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
Eyeshields, Gloves, type N95 (US)
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Abdou Saad El-Tabl et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 71(1), 90-99 (2008-02-05)
A new series of mono and binuclear Mn(II), Fe(III), Co(II), Ni(II), Cu(II), Zn(II), La(III), Ru(III), Hf(IV), ZrO(II) and UO2(II) complexes of phenylaminodibenzoylhydrazone have been synthesized and characterized by elementals analyses, IR UV-vis spectra, magnetic moments, conductances, thermal analyses (DTA and
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
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
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
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