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FLAVONE

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FLAVONE Basic information

Product Name:
FLAVONE
Synonyms:
  • Cromaril
  • DA6034
  • Flavon
  • Phenylchromone
  • Flavone(2-Phenylchromone)
  • 2-Phenyl-γ-benzopyrone
  • 4H-1-Benzopyran-4-one, 2-phenyl-
  • 4H-1-Benzopyran-4-one,2-phenyl-
CAS:
525-82-6
MF:
C15H10O2
MW:
222.24
EINECS:
208-383-8
Product Categories:
  • Building block
  • Biochemistry
  • Flavonoids
  • Inhibitors
  • Elisa Kit-plant ELISA Kit
Mol File:
525-82-6.mol
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FLAVONE Chemical Properties

Melting point:
94-97 °C (lit.)
Boiling point:
185 °C / 1mmHg
Density 
1.1404 (rough estimate)
refractive index 
1.6600 (estimate)
storage temp. 
Sealed in dry,Room Temperature
solubility 
>38.3 mg/mL in EtOH; >52.3 mg/mL in DMSO
form 
Crystalline Powder
color 
White
Water Solubility 
Soluble in acetone (25 mg/ml), methanol, alcohol, and chloroform. Insoluble in water.
Merck 
14,4092
BRN 
157598
LogP
3.560
CAS DataBase Reference
525-82-6(CAS DataBase Reference)
EPA Substance Registry System
Flavone (525-82-6)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
2
RTECS 
DJ3100630
Hazard Note 
Irritant
TSCA 
Yes
HS Code 
29329990

MSDS

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FLAVONE Usage And Synthesis

Chemical Properties

white crystalline powder

Uses

Flavone is a potentially useful biochemical for cytochrome P450 studies.

Definition

One of a group of flavonoid plant pigments existing as colorless needles, that are insoluble in water and melting at 100C. It fluoresces violet in concentrated sulfuric acid. It can be synthesized. Treatment with alcoholic alkali yields flavanone. The fla

Synthesis Reference(s)

Journal of the American Chemical Society, 79, p. 689, 1957 DOI: 10.1021/ja01560a050
The Journal of Organic Chemistry, 44, p. 497, 1979 DOI: 10.1021/jo01318a005
Tetrahedron Letters, 31, p. 4073, 1990 DOI: 10.1016/S0040-4039(00)94503-9

Purification Methods

Dissolve it in dilute aqueous NaOH, filter and precipitate it by adding dilute (1:1) HCl. The process is repeated twice more, and the fluorescein is dried at 100o. Alternatively, it has been crystallised from acetone by allowing the solution to evaporate at 37o in an open beaker. It has also been recrystallised from EtOH and dried in a vacuum oven. [Beilstein 19 I 721, 19 II 248, 19 III/IV 2904, 19/8 V 456.]

FLAVONESupplier

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