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D204609

Sigma-Aldrich

1,3-Diphenyl-2-propanone

99%

Synonym(s):

1,3-Diphenylacetone, Dibenzyl ketone

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About This Item

Linear Formula:
(C6H5CH2)2CO
CAS Number:
102-04-5
Molecular Weight:
210.27
Beilstein:
974767
EC Number:
203-000-0
MDL number:
MFCD00004795
UNSPSC Code:
12352100
PubChem Substance ID:
24893606
NACRES:
NA.22

Assay

99%

form

solid

bp

330 °C (lit.)

mp

32-34 °C (lit.)

SMILES string

O=C(Cc1ccccc1)Cc2ccccc2

InChI

1S/C15H14O/c16-15(11-13-7-3-1-4-8-13)12-14-9-5-2-6-10-14/h1-10H,11-12H2

InChI key

YFKBXYGUSOXJGS-UHFFFAOYSA-N

Gene Information

human ... EPHX2(2053)
mouse ... Ephx2(13850)

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Application

1,3-Diphenyl-2-propanone is used as a precursor to synthesize structurally defined, fluorescent polyphenylene dendrimers as light emitters for organic light emitting diodes. It is also used in the synthesis of several other polycyclic aromatic hydrocarbons and conjugated polymers.

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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New hyperbranched conjugated polymers containing hexaphenylbenzene and oxadiazole units: convenient synthesis and efficient deep blue emitters for PLEDs application.
Li Z A, et al.
The Journal of Physical Chemistry B, 114(28), 9101-9108 (2010)
Polytriphenylene Dendrimers: A Unique Design for Blue?Light?Emitting Materials.
Qin T, et al.
Angewandte Chemie (Weinheim an der Bergstrasse, Germany), 120(43), 8416-8420 (2008)
Configurationally stable longitudinally twisted polycyclic aromatic compounds.
Walters R S, et al.
Journal of the American Chemical Society, 130(48), 16435-16441 (2008)
Triphenylene-based polymers for blue polymeric light emitting diodes.
Saleh M, et al.
Macromolecules, 43(1), 137-143 (2009)
Structurally-defined, sulfo-phenylated, oligophenylenes and polyphenylenes.
Skalski T J, et al.
Journal of the American Chemical Society, 137(38), 12223-12226 (2015)
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