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B56609

9-Bromoanthracene

Name: 9-Bromoanthracene
Brand: ALDRICH

94%

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About This Item

Formula empirica (notazione di Hill):

C₁₄H₉Br

Numero CAS:

1564-64-3

Peso molecolare:

257.13

Beilstein:

1869747

Numero CE:

216-359-3

Numero MDL:

MFCD00001243

Codice UNSPSC:

12352100

ID PubChem:

24891852

NACRES:

NA.22

Saggio

94%

Forma fisica

crystals

Punto di fusione

97-100 °C (lit.)

Stringa SMILE

Brc1c2ccccc2cc3ccccc13

InChI

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

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Categorie correlate

Building block organici

Chimica e biochimica

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

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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

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

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

Cumulative health risk assessment of halogenated and parent polycyclic aromatic hydrocarbons associated with particulate matters in urban air.

Jian-Lin Sun et al.

Ecotoxicology and environmental safety, 113, 31-37 (2014-12-09)

Halogenated polycyclic aromatic hydrocarbons (HPAHs) have been reported to occur widely in urban air. Nevertheless, knowledge about the human health risk associated with inhalation exposure to HPAHs is scarce so far. In the present study, nine HPAHs and 16 PAHs

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