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BCR272

Coronen

BCR®, certified reference material

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About This Item

Empirische Formel (Hill-System):
C24H12
CAS-Nummer:
Molekulargewicht:
300.35
Beilstein:
658468
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
41116107
PubChem Substanz-ID:
NACRES:
NA.24

Qualität

certified reference material

Agentur

BCR®

Hersteller/Markenname

JRC

Methode(n)

HPLC: suitable
gas chromatography (GC): suitable

bp

525 °C (lit.)

mp (Schmelzpunkt)

428 °C (lit.)

Format

neat

Lagertemp.

2-8°C

SMILES String

c1cc2ccc3ccc4ccc5ccc6ccc1c7c2c3c4c5c67

InChI

1S/C24H12/c1-2-14-5-6-16-9-11-18-12-10-17-8-7-15-4-3-13(1)19-20(14)22(16)24(18)23(17)21(15)19/h1-12H

InChIKey

VPUGDVKSAQVFFS-UHFFFAOYSA-N

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Hinweis zur Analyse

For more information please see:
BCR272

Rechtliche Hinweise

BCR is a registered trademark of European Commission

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)


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Analysenzertifikate (COA)

Lot/Batch Number

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Long Chen et al.
Journal of the American Chemical Society, 134(43), 17869-17872 (2012-10-16)
Here we report hexathienocoronenes (HTCs), fully thiophene-annelated coronenes in which six double bonds in the periphery are thieno-fused. The derivatives tetrasubstituted with hexyl and dodecyl chains show a phase formation that strongly depends on the chain length. HTCs are remarkably
Marco Franceschin et al.
ChemMedChem, 7(12), 2144-2154 (2012-10-26)
Based on previous work on both perylene and coronene derivatives as G-quadruplex binders, a novel chimeric compound was designed: N,N'-bis[2-(1-piperidino)-ethyl]-1-(1-piperidinyl)-6-[2-(1-piperidino)-ethyl]-benzo[ghi]perylene-3,4:9,10-tetracarboxylic diimide (EMICORON), having one piperidinyl group bound to the perylene bay area (positions 1, 12 and 6, 7 of the
A versatile Fréchet-dendron compound unifies host-guest and templated heterogeneous self-assembly.
Kathrin Gruber et al.
Advanced materials (Deerfield Beach, Fla.), 23(19), 2195-2198 (2011-04-07)
Anna M Hiszpanski et al.
ACS nano, 7(1), 294-300 (2012-12-12)
The structuring in organic electrically active thin films critically influences the performance of devices comprising them. Controlling film structure, however, remains challenging and generally requires stringent deposition conditions or modification of the substrate. To this end, we have developed post-deposition
Seok Ju Kang et al.
Angewandte Chemie (International ed. in English), 51(34), 8594-8597 (2012-07-19)
"Ball and socket" motif: The contorted dibenzotetrathienocoronene (6-DBTTC) forms a complex with the C(70) fullerene PC(70) BM embedded in an amorphous phase of PC(70) BM. The materials are processable into organic solar cells in solution. The power conversion efficiency is

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