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D33454

Sigma-Aldrich

1,3-Diphenyl-1,3-propanedione

98%

Synonyme(s) :

Dibenzoylmethane

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About This Item

Formule linéaire :
(C6H5CO)2CH2
Numéro CAS:
120-46-7
Poids moléculaire :
224.25
Numéro Beilstein :
514910
Numéro CE :
204-398-9
Numéro MDL:
MFCD00003085
Code UNSPSC :
12352100
ID de substance PubChem :
24893746
Nomenclature NACRES :
NA.22

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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Catégories apparentées

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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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
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
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
Preetha Anand et al.
Biochemical pharmacology, 82(12), 1901-1909 (2011-09-20)
Curcumin, a diferuloylmethane, has been shown to exhibit anti-inflammatory and anti-proliferative activities. Whereas curcumin has both a Michael acceptor and a Michael donor units, its analogues dibenzoylmethane (DBM, a component of licorice) and dibenzoylpropane (DBP) have a Michael donor but
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