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362069

Sigma-Aldrich

1,3-Dibenzoylpropane

98%

Synonym(s):

1,5-Diphenyl-1,5-pentanedione

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About This Item

Linear Formula:
C6H5CO(CH2)3COC6H5
CAS Number:
6263-83-8
Molecular Weight:
252.31
MDL number:
MFCD00051401
UNSPSC Code:
12352100
PubChem Substance ID:
24862289
NACRES:
NA.22

Assay

98%

form

solid

mp

66-68 °C (lit.)

SMILES string

O=C(CCCC(=O)c1ccccc1)c2ccccc2

InChI

1S/C17H16O2/c18-16(14-8-3-1-4-9-14)12-7-13-17(19)15-10-5-2-6-11-15/h1-6,8-11H,7,12-13H2

InChI key

YOLLTWVIOASMFW-UHFFFAOYSA-N

Related Categories

General description

1,3-Dibenzoylpropane is a 1,3-diaroylpropane. 1,3-Dibenzoylpropane is formed during hydroxocobalt(III) Schiff base complexes catalyzed selective aldol reaction of dibenzoylmethanes with formaldehyde in methanol.

Application

1,3-Dibenzoylpropane may be used in the electrochemical synthesis of cis-1,2-diphenyl-1,2-cyclopentanediol, via reduction in acetonitrile.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Highly selective aldol reaction of dibenzoylmethanes with formaldehyde catalyzed by cobalt Schiff base complex under neutral conditions.
Maruyama K, et al.
Tetrahedron Letters, 36(31), 5609-5612 (1995)
Electrochemical cyclization: II. Intramolecular pinacolization of 1, 3-dibenzoylpropane in acetonitrile.
Ammar F, et al.
J. Electroanal. Chem. Interfac. Electrochem., 53(3), 407-416 (1974)

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