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236373

Sigma-Aldrich

Dibenzofuran

98%

Synonym(s):

Diphenylene oxide

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$71.60
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10 G
$71.60
50 G
$237.00

About This Item

Empirical Formula (Hill Notation):
C12H8O
CAS Number:
132-64-9
Molecular Weight:
168.19
Beilstein/REAXYS Number:
121100
EC Number:
205-071-3
MDL number:
MFCD00004968
UNSPSC Code:
12352100
PubChem Substance ID:
24854168
NACRES:
NA.22

$71.60

Available to ship onApril 29, 2025Details

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Quality Level

100

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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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[1]. Biodegradation of dibenzofuran (DF) and its structural analogs by a newly isolated Agrobacterium sp. PH-08 has been reported[2].

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKCW3845
MKCN1772
MKCL9861
MKCG3700
MKCD9952

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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
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
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
Ulrika Nordlöf et al.
The Science of the total environment, 438, 166-173 (2012-09-25)
Concentrations of polychlorinated dibenzo-p-dioxins (PCDD), polychlorinated dibenzofurans (PCDF), and dioxin-like non-ortho-PCBs were measured in white-tailed sea eagle (WTSE) eagle eggs collected along the Swedish coast of the Baltic Sea during the period 1992-2004. The eggs represent two different subpopulations with
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