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BCR272

Coronene

BCR®, certified reference material

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About This Item

Empirical Formula (Hill Notation):
C24H12
CAS Number:
191-07-1
Molecular Weight:
300.35
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
329773805
EC Number:
205-881-7
Beilstein/REAXYS Number:
658468
MDL number:
MFCD00004134

Key Documents

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InChI key

VPUGDVKSAQVFFS-UHFFFAOYSA-N

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

SMILES string

c1cc2ccc3ccc4ccc5ccc6ccc1c7c2c3c4c5c67

grade

certified reference material

agency

BCR®

manufacturer/tradename

JRC

technique(s)

HPLC: suitable, gas chromatography (GC): suitable

bp

525 °C (lit.)

mp

428 °C (lit.)

format

neat

storage temp.

2-8°C

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Analysis Note

For more information please see:
BCR272

Legal Information

BCR is a registered trademark of European Commission

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

Certificates of Analysis (COA)

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Di Wu et al.
The Journal of organic chemistry, 77(24), 11319-11324 (2012-11-29)
The construction of coronenes using simple building blocks is a challenging task. In this work, triphenylene was used as a building block to construct functionalized coronenes, and their solid structures and optoelectronic properties were investigated. The single crystal structures showed
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
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)
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
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