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BCR272

晕苯

BCR®, certified reference material

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About This Item

经验公式（希尔记法）:
C24H12
CAS号:
191-07-1
分子量:
300.35
Beilstein:
658468
EC 号:
205-881-7
MDL编号:
MFCD00004134
UNSPSC代码:
41116107
PubChem化学物质编号:
329773805
NACRES:
NA.24

等级

certified reference material

Agency

BCR®

制造商/商品名称

JRC

技术

HPLC: suitable
gas chromatography (GC): suitable

沸点

525 °C (lit.)

mp

428 °C (lit.)

包装形式

neat

储存温度

2-8°C

SMILES字符串

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

InChI key

VPUGDVKSAQVFFS-UHFFFAOYSA-N

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分析说明

For more information please see:
BCR272

法律信息

BCR is a registered trademark of European Commission

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, type N95 (US)

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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红荧烯 sublimed grade, 99.99% trace metals basis

Sigma-Aldrich

551112

红荧烯

多环芳烃 (PAH) 校准混标 TraceCERT®, certified reference material, 10 μg/mL each component in acetonitrile

Supelco

CRM47940

多环芳烃 (PAH) 校准混标

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
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
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
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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