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5 G
RM 512.00
About This Item
Empirical Formula (Hill Notation):
C9H6O2
CAS Number:
Molecular Weight:
146.14
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Assay:
99%
Recommended Products
Quality Level
Assay
99%
mp
55-60 °C (lit.)
functional group
ketone
SMILES string
O=C1C=COc2ccccc12
InChI
1S/C9H6O2/c10-8-5-6-11-9-4-2-1-3-7(8)9/h1-6H
InChI key
OTAFHZMPRISVEM-UHFFFAOYSA-N
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General description
The compounds with chromone skeleton exhibits antiradical activities that provide protection against oxidative stress[1].
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
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The interaction between leukocytes and the vascular endothelial cells (EC) via cellular adhesion molecules plays an important role in various inflammatory and immune diseases. The molecules that block these interactions have been targeted as potential therapeutic targets for acute and
Aleksandra Kładna et al.
Luminescence : the journal of biological and chemical luminescence, 29(7), 846-853 (2014-02-01)
Recent reviews evidence that the naturally occurring compounds containing the chromone skeleton exhibit antiradical activities, providing protection against oxidative stress. The antioxidant activities of 13 new synthesized chromonyl-2,4-thiazolidinediones, chromonyl-2,4-imidazolidinediones and chromonyl-2-thioxoimidzolidine-4-ones were evaluated using in vitro antioxidant assays, including superoxide
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Scientific reports, 10(1), 13457-13457 (2020-08-12)
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