Fortfahren mit
45775
Dibenzofuran
analytical standard
Synonym(e):
Diphenylenoxid
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Über diesen Artikel
Empirische Formel (Hill-System):
C12H8O
CAS-Nummer:
Molekulargewicht:
168.19
EC Number:
205-071-3
UNSPSC Code:
41116107
PubChem Substance ID:
Beilstein/REAXYS Number:
121100
MDL number:
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Unterstützung erhaltengrade
analytical standard
Quality Segment
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
bp
154-155 °C/20 mmHg (lit.)
mp
80-82 °C (lit.)
application(s)
environmental
format
neat
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
Application
Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
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Lagerklasse
11 - Combustible Solids
wgk
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
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral
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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
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