3-Hydroxyflavone, 98+%
3-Hydroxyflavone, 98+%
3-Hydroxyflavone, 98+%
3-Hydroxyflavone, 98+%
Thermo Scientific Chemicals

3-Hydroxyflavone, 98+%

CAS: 577-85-5 | C15H10O3 | 238.24 g/mol
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1 g
5 g
Catalog number A18110.03
also known as A18110-03
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Quantity:
1 g
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Price (EUR)
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Chemical Identifiers
CAS577-85-5
SpecificationsSpecification SheetSpecification Sheet
Melting Point (clear melt)168.0-174.0°C
Appearance (Color)White to yellow or pale cream
Assay (HPLC)≥98.0%
FormPowder
3-Hydroxyflavone is a reactant involved in studies of photochemically-induced dioxygenase-type CO-release reactivity; phase-transfer protection and deprotection of hydroxychromones; and O-methylation with di-Me carbonate. As a reactant it is involved in the synthesis of biologically active molecules including 2-chloropyridine derivatives for studies of antitumor agents and telomerase inhibitors; dihydrochromenopyrazines and chromenoquinoxalines. It is also involved in studies of its electrochemical properties using voltammetric methodologies.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
3-Hydroxyflavone is a reactant involved in studies of photochemically-induced dioxygenase-type CO-release reactivity; phase-transfer protection and deprotection of hydroxychromones; and O-methylation with di-Me carbonate. As a reactant it is involved in the synthesis of biologically active molecules including 2-chloropyridine derivatives for studies of antitumor agents and telomerase inhibitors; dihydrochromenopyrazines and chromenoquinoxalines. It is also involved in studies of its electrochemical properties using voltammetric methodologies.

Solubility
Insoluble in water. Soluble in N,N-DMF and ethanol.

Notes
Stable under recommended storage conditions. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. Katarzyna Grubel; Brynna J.Laughlin; Thora R.Maltais; Rhett C.Smith; Atta M.Arif, Lisa M.Berreau. Photochemically-induced dioxygenase-type CO-release reactivity of group 12 metal flavonolate complexes. Chemical Communications. 2011, 47,(37), 10431-10433.
  2. Xin-Hua Liu; Hui-Feng Liu; Xu Shen; Bao-An Song; Pinaki S.Bhadury; Hai-Liang Zhu; Jin-Xing Liu; Xing-Bao Qi. Synthesis and molecular docking studies of novel 2-chloro-pyridine derivatives containing flavone moieties as potential antitumor agents. Bioorganic & Medicinal Chemistry Letters. 2010, 20,(14), 4163-4167.