BCR337
Dibenzo[b,d]furan
BCR®, certified reference material
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About This Item
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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
BCR337
Legal Information
BCR is a registered trademark of European Commission
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
266.0 °F - closed cup
Flash Point(C)
130 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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
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
The effect of the substitution position of dibenzofuran on the photophysical and charge-transport properties of host materials for phosphorescent organic light-emitting diodes.
Chemistry (Weinheim an der Bergstrasse, Germany), 19(4), 1194-1198 (2012-12-21)
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
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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