Skip to Content
Merck
CN

808245

10,10′-dibromo-9,9′-bianthracene

Synonym(s):

10,10′-dibromo-9,9′-bianthryl, 10-bromo-9-(10-bromoanthracen-9-yl)anthracene

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Empirical Formula (Hill Notation):
C28H16Br2
CAS Number:
121848-75-7
Molecular Weight:
512.23
NACRES:
NA.23
PubChem Substance ID:
329769060
UNSPSC Code:
12352103
MDL number:
MFCD11045035

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

InChI

1S/C28H16Br2/c29-27-21-13-5-1-9-17(21)25(18-10-2-6-14-22(18)27)26-19-11-3-7-15-23(19)28(30)24-16-8-4-12-20(24)26/h1-16H

SMILES string

BrC1=C2C(C=CC=C2)=C(C3=C(C=CC=C4)C4=C(Br)C5=C3C=CC=C5)C6=CC=CC=C61

InChI key

NPNNLGXEAGTSRN-UHFFFAOYSA-N

assay

≥98% (HPLC)

form

powder

mp

348-352 °C

Quality Level

100

Related Categories

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCM5016

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Yen-Chia Chen et al.
Nature nanotechnology, 10(2), 156-160 (2015-01-13)
Bandgap engineering is used to create semiconductor heterostructure devices that perform processes such as resonant tunnelling and solar energy conversion. However, the performance of such devices degrades as their size is reduced. Graphene-based molecular electronics has emerged as a candidate
Surface-Assisted Reactions toward Formation of Graphene Nanoribbons on Au(110) Surface.
Lorenzo M, et al.
The Journal of Physical Chemistry C, 119(5), 2427-2437 (2015)
Akimitsu Narita et al.
Chemical record (New York, N.Y.), 15(1), 295-309 (2014-11-22)
In this article, we describe our chemical approach, developed over the course of a decade, towards the bottom-up synthesis of structurally well-defined graphene nanoribbons (GNRs). GNR synthesis can be achieved through two different methods, one being a solution-phase process based

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service