Wszystkie zdjęcia(3)
Key Documents
D33454
1,3-Diphenyl-1,3-propanedione
98%
Synonim(y):
Dibenzoylmethane
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About This Item
Wzór liniowy:
(C6H5CO)2CH2
Numer CAS:
Masa cząsteczkowa:
224.25
Beilstein:
514910
Numer WE:
Numer MDL:
Kod UNSPSC:
12352100
Identyfikator substancji w PubChem:
NACRES:
NA.22
Polecane produkty
Poziom jakości
Próba
98%
Postać
crystals
tw
219-221 °C/18 mmHg (lit.)
mp
77-79 °C (lit.)
ciąg 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
Klucz InChI
NZZIMKJIVMHWJC-UHFFFAOYSA-N
informacje o genach
human ... ACHE(43) , BCHE(590) , CES1(1066)
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Opis ogólny
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.
Zastosowanie
- 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).
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Kod klasy składowania
11 - Combustible Solids
Klasa zagrożenia wodnego (WGK)
WGK 3
Temperatura zapłonu (°F)
Not applicable
Temperatura zapłonu (°C)
Not applicable
Środki ochrony indywidualnej
Eyeshields, Gloves, type N95 (US)
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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.
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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