D33454
1,3-Diphenyl-1,3-propanedione
98%
Synonym(s):
Dibenzoylmethane
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About This Item
Linear Formula:
(C6H5CO)2CH2
CAS Number:
Molecular Weight:
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
Quality Segment
assay
98%
form
crystals
bp
219-221 °C/18 mmHg (lit.)
mp
77-79 °C (lit.)
SMILES string
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
InChI key
NZZIMKJIVMHWJC-UHFFFAOYSA-N
Gene Information
human ... ACHE(43), BCHE(590), CES1(1066)
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.
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).
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Storage Class
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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