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B56609

9-Bromoanthracene

Name: 9-Bromoanthracene
Brand: ALDRICH

94%

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About This Item

Empirical Formula (Hill Notation):

C₁₄H₉Br

CAS Number:

1564-64-3

Molecular Weight:

257.13

UNSPSC Code:

12352100

NACRES:

NA.22

PubChem Substance ID:

24891852

EC Number:

216-359-3

Beilstein/REAXYS Number:

1869747

MDL number:

MFCD00001243

Assay:

94%

Form:

crystals

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Properties

Quality Level

100

assay

94%

form

crystals

mp

97-100 °C (lit.)

SMILES string

Brc1c2ccccc2cc3ccccc13

InChI

1S/C14H9Br/c15-14-12-7-3-1-5-10(12)9-11-6-2-4-8-13(11)14/h1-9H

InChI key

ZIRVQSRSPDUEOJ-UHFFFAOYSA-N

Description

Storage Class

11 - Combustible Solids

wgk

WGK 2

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

pictograms

GHS09

signalword

Warning

hcodes

H410

pcodes

P273 - P391 - P501

Hazard Classifications

Aquatic Acute 1 - Aquatic Chronic 1

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Photophysical properties of symmetrically substituted diarylacetylenes and diarylbuta-1,3-diynes.

Irena Bylińska et al.

Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 15(1), 45-56 (2015-12-01)

A series of symmetrically substituted diarylacetylenes and diaryl-1,3-butadiynes were prepared and studied with an emphasis on their spectral and photophysical properties. The photophysical characteristics of these compounds were studied in relation to their structures and the influence of solvent or

Synthesis and properties of blue luminescent bipolar materials constructed with carbazole and anthracene units with 4-cyanophenyl substitute at the 9-position of the carbazole unit.

Pengbo Xie et al.

Luminescence : the journal of biological and chemical luminescence, 33(3), 604-610 (2018-01-30)

With carbazole and p-cyanobromobenzene as raw materials, 4-(3,6-di (anthracen-9-yl)-9H-carbazol-9-yl)benzonitrile (DACB) and 4-(3,6-bis(anthracene -9-ylethynyl)-9H-carbazol-9-yl)benzonitrile (BACB) were synthesized through the Suzuki coupling reaction and the Sonogashira coupling reaction, respectively. These structures were characterized using 1 H nuclear magnetic resonance (NMR), elemental analysis

Congener-specific determination of ultratrace levels of chlorinated and brominated polycyclic aromatic hydrocarbons in atmosphere and industrial stack gas by isotopic dilution gas chromatography/high resolution mass spectrometry method.

Rong Jin et al.

Journal of chromatography. A, 1509, 114-122 (2017-06-18)

Isotopic dilution gas chromatography combined with high resolution mass spectrometry (GC/HRMS) has overwhelming advantages with respect to the accuracy of congener-specific ultratrace analysis of complex persistent organic pollutants (POPs) in environmental matrices. However, an isotopic dilution GC/HRMS method for analysis

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Global Trade Item Number

SKU	GTIN
B56609-5G	04061833434048
B56609-25G	04061833434031