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F2003

Sigma-Aldrich

Flavone

≥99.0%

Synonym(s):

2-Phenyl-4H-1-benzopyran-4-one, 2-Phenylchromone

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About This Item

Empirical Formula (Hill Notation):
C15H10O2
CAS Number:
525-82-6
Molecular Weight:
222.24
Beilstein:
157598
EC Number:
208-383-8
MDL number:
MFCD00006825
UNSPSC Code:
12352100
PubChem Substance ID:
57654180
NACRES:
NA.22

Assay

≥99.0%

form

powder

mp

94-97 °C (lit.)

SMILES string

O=C1C=C(Oc2ccccc12)c3ccccc3

InChI

1S/C15H10O2/c16-13-10-15(11-6-2-1-3-7-11)17-14-9-5-4-8-12(13)14/h1-10H

InChI key

VHBFFQKBGNRLFZ-UHFFFAOYSA-N

Gene Information

human ... ADORA3(140) , ANPEP(290) , CYP1A2(1544)
mouse ... Hexa(15211)
rat ... Adora1(29290) , Adora2a(25369) , Ar(24208) , Gabra2(29706)

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Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 2

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Sigma-Aldrich

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The kinetics for the reactions of hypoiodous acid (HOI) with various phenols (phenol, 4-nitrophenol, 4-hydroxybenzoic acid), 3-oxopentanedioic acid (3-OPA) and flavone were investigated in the pH range of 6.0-11.0. The apparent second order rate constants for the reactions of HOI
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Gray leaf spot (GLS) disease in maize, caused by the fungus Cercospora zeina, is a threat to maize production globally. Understanding the molecular basis for quantitative resistance to GLS is therefore important for food security. We developed a de novo
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