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Documenti fondamentali

236373

Sigma-Aldrich

Dibenzofuran

98%

Sinonimo/i:

Diphenylene oxide

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About This Item

Formula empirica (notazione di Hill):
C12H8O
Numero CAS:
Peso molecolare:
168.19
Beilstein:
121100
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prezzi e disponibilità al momento non sono disponibili

Livello qualitativo

Saggio

98%

Stato

solid

P. ebollizione

154-155 °C/20 mmHg (lit.)

Punto di fusione

80-82 °C (lit.)

Solubilità

acetic acid: soluble(lit.)
benzene: soluble(lit.)
diethyl ether: soluble(lit.)
ethanol: soluble(lit.)
water: insoluble(lit.)

Stringa SMILE

c1ccc2c(c1)oc3ccccc23

InChI

1S/C12H8O/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8H
TXCDCPKCNAJMEE-UHFFFAOYSA-N

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Descrizione generale

Dibenzofuran has been converted to a vacuum-sublimable, electron-transporting host material for blue-green electrophosphorescent molecule, iridium (III) bis(4,6-(di-fluorophenyl)pyridinato-N,C2′)picolinate[1]. Biodegradation of dibenzofuran (DF) and its structural analogs by a newly isolated Agrobacterium sp. PH-08 has been reported[2].

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

266.0 °F - closed cup

Punto d’infiammabilità (°C)

130 °C - closed cup

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Certificati d'analisi (COA)

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Sigma-Aldrich

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Fluorene 98%

Sigma-Aldrich

128333

Fluorene

Acridine ≥96.5% (HPLC)

Sigma-Aldrich

A23609

Acridine

Acenaftene 99%

Sigma-Aldrich

215376

Acenaftene

Paul A Vecchi et al.
Organic letters, 8(19), 4211-4214 (2006-09-08)
Dibenzofuran (DBF) is converted to a vacuum-sublimable, electron-transporting host material via 2,8-substitution with diphenylphosphine oxide moieties. Close pi-pi stacking and the inductive influence of P=O moieties impart favorable electron-transport properties without lowering the triplet energy. A maximum external quantum efficiency
T T Le et al.
Journal of applied microbiology, 116(3), 542-553 (2013-11-28)
To demonstrate the biodegradation of dibenzofuran (DF) and its structural analogs by a newly isolated Agrobacterium sp. PH-08. To assess the biodegradation potential of newly isolated Agrobacterium sp. PH-08, various substrates were evaluated as sole carbon sources in growth and
Markus Hauck et al.
Annals of botany, 103(1), 13-22 (2008-11-04)
Many species of lichen-forming fungi contain yellow or orange extracellular pigments belonging to the dibenzofurans (usnic acid), anthraquinones (e.g. parietin) or pulvinic acid group. These pigments are all equally efficient light screens, leading us to question the potential ecological and
D Zacs et al.
Chemosphere, 91(2), 179-186 (2013-01-23)
Seventeen polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDD/PCDFs) of the highest priority as well as twelve dioxin-like polychlorinated biphenyls (dl-PCBs) were analyzed in the muscle tissues of the following freshwater fish species sampled from eleven Latvian freshwater lakes: perch (Perca flavescens)
Jing Pan et al.
Bulletin of environmental contamination and toxicology, 89(6), 1240-1246 (2012-09-26)
The concentrations of polychlorinated dibenzo-p-dioxins/dibenzofurans (PCDD/Fs), dioxin-like polychlorinated biphenyls (PCBs), and polychlorinated naphthalenes (PCNs) were measured in two sediment cores collected from Jiaozhou Bay. The concentrations of PCDD/Fs, dioxin-like PCBs, and PCNs in the cores were in the range of

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