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T25801

Sigma-Aldrich

Tetraphenylcyclopentadienone

98%

Synonym(s):

2,3,4,5-Tetraphenyl-2,4-cyclopentadien-1-one, 2,3,4,5-Tetraphenylcyclopenta-2,4-dienone, 2,3,4,5-Tetraphenylcyclopentadienone, Cyclone

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About This Item

Empirical Formula (Hill Notation):
C29H20O
CAS Number:
479-33-4
Molecular Weight:
384.47
Beilstein:
683115
EC Number:
207-530-3
MDL number:
MFCD00001407
UNSPSC Code:
12352100
PubChem Substance ID:
24900046
NACRES:
NA.22

Assay

98%

mp

217-220 °C (lit.)

SMILES string

O=C1C(c2ccccc2)=C(c3ccccc3)C(c4ccccc4)=C1c5ccccc5

InChI

1S/C29H20O/c30-29-27(23-17-9-3-10-18-23)25(21-13-5-1-6-14-21)26(22-15-7-2-8-16-22)28(29)24-19-11-4-12-20-24/h1-20H

InChI key

PLGPSDNOLCVGSS-UHFFFAOYSA-N

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Related Categories

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)

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Journal of the American Chemical Society, 129(15), 4595-4605 (2007-03-24)
Two routes for the introduction of highly fluorescent peryleneimide chromophores into the scaffolding of polyphenylene dendrimers via iterative Diels-Alder cycloadditions are presented. The key intermediates for the divergent dendrimer buildup were two cyclopentadienone branching units carrying two peryleneimides and two
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Chemistry (Weinheim an der Bergstrasse, Germany), 22(39), 14013-14021 (2016-08-10)
A new class of ruthenium(II) polypyridine complexes with a series of D-π-A-π-D type (D=donor, A=acceptor) ligands was synthesized and characterized by

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