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Merck
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주요 문서

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236373

Sigma-Aldrich

Dibenzofuran

98%

동의어(들):

Diphenylene oxide

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모든 사진(2)

About This Item

실험식(Hill 표기법):
C12H8O
CAS Number:
132-64-9
Molecular Weight:
168.19
Beilstein:
121100
EC Number:
205-071-3
MDL number:
MFCD00004968
UNSPSC 코드:
12352100
PubChem Substance ID:
24854168
NACRES:
NA.22

Quality Level

100

분석

98%

양식

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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관련 카테고리

일반 설명

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 Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

266.0 °F - closed cup

Flash Point (°C)

130 °C - closed cup

개인 보호 장비

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

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시험 성적서(COA)

Lot/Batch Number
MKCN1772
MKCL9861
MKCG3700
MKCD9952
MKBW2691V

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Sigma-Aldrich

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Acridine ≥96.5% (HPLC)

Sigma-Aldrich

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Acenaphthene 99%

Sigma-Aldrich

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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
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
José L Domingo et al.
Environment international, 50, 22-30 (2012-10-04)
The concentrations of polychlorinated dibenzo-p-dioxins and polychlorinated dibenzofurans (PCDD/Fs) were determined in a number of foodstuffs purchased in various locations near a hazardous waste incinerator (HWI) in Tarragona County (Catalonia, Spain). The dietary intake of PCDD/Fs by the population of
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