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Documentos

236373

Sigma-Aldrich

Dibenzofuran

98%

Sinónimos:

Diphenylene oxide

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About This Item

Fórmula empírica (notación de Hill):
C12H8O
Número de CAS:
132-64-9
Peso molecular:
168.19
Beilstein/REAXYS Number:
121100
EC Number:
205-071-3
MDL number:
MFCD00004968
UNSPSC Code:
12352100
PubChem Substance ID:
24854168
NACRES:
NA.22

assay

98%

form

solid

bp

154-155 °C/20 mmHg (lit.)

mp

80-82 °C (lit.)

solubility

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

SMILES string

c1ccc2c(c1)oc3ccccc23

InChI

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

InChI key

TXCDCPKCNAJMEE-UHFFFAOYSA-N

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Categorías relacionadas

General description

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. Biodegradation of dibenzofuran (DF) and its structural analogs by a newly isolated Agrobacterium sp. PH-08 has been reported.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

266.0 °F - closed cup

flash_point_c

130 °C - closed cup

ppe

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

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Sigma-Aldrich

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Sigma-Aldrich

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Fluorene

Acridine ≥96.5% (HPLC)

Sigma-Aldrich

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Acenafteno 99%

Sigma-Aldrich

215376

Acenafteno

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
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
Ruud P M Dings et al.
The Journal of pharmacology and experimental therapeutics, 344(3), 589-599 (2012-12-13)
Galectin-1 (gal-1), which binds β-galactoside groups on various cell surface receptors, is crucial to cell adhesion and migration, and is found to be elevated in several cancers. Previously, we reported on 6DBF7, a dibenzofuran (DBF)-based peptidomimetic of the gal-1 antagonist
Jannie Christensen et al.
Chemistry, an Asian journal, 8(3), 648-652 (2012-12-15)
An intramolecular, organocatalyzed Michael addition has been developed to obtain biologically important 2,3-disubstituted cis-2,3-dihydrobenzofurans. By using mandelic acid salts of primary aminocatalysts, derived from cinchona alkaloids, the intramolecular cyclization reaction has been developed to proceed in high yield, with moderate
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
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