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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/REAXYS Number:
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

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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)
Structurally-defined, sulfo-phenylated, oligophenylenes and polyphenylenes.
Skalski T J, et al.
Journal of the American Chemical Society, 137(38), 12223-12226 (2015)
Triphenylene-based polymers for blue polymeric light emitting diodes.
Saleh M, et al.
Macromolecules, 43(1), 137-143 (2009)
Fluoranthene derivatives as blue fluorescent materials for non-doped organic light-emitting diodes.
Kumar S, et al.
J. Mater. Sci., 4(1), 193-200 (2016)
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