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BCR337

Dibenzo[b,d]furan

BCR®, certified reference material

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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:
41116107
PubChem Substance ID:
329773822
NACRES:
NA.24

grade

certified reference material

agency

BCR®

manufacturer/tradename

JRC

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

format

neat

storage temp.

2-8°C

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

Analysis Note

For more information please see:
BCR337

Legal Information

BCR is a registered trademark of European Commission

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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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
Juan A Conesa et al.
Chemosphere, 91(2), 118-123 (2012-12-13)
Combustion runs at 700 °C in a horizontal laboratory furnace were carried out on two different electric wires (PVC and halogen-free wire). Tests were performed in the presence and in the absence of the metal conductor of the wires. The
Jürgen Wittsiepe et al.
Journal of toxicology and environmental health. Part A, 75(8-10), 423-428 (2012-06-13)
Levels of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/F) were determined in 23 blood samples of exposed workers from a transformer recycling plant in Dortmund, Germany. Compared to the most recent studies on German background levels of adults, elevated concentrations of up
The effect of the substitution position of dibenzofuran on the photophysical and charge-transport properties of host materials for phosphorescent organic light-emitting diodes.
Chil Won Lee et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 19(4), 1194-1198 (2012-12-21)
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
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