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3-Hydroxyflavone, 98+%, Thermo Scientific Chemicals

Catalog Number p-7023995
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Quantity:
1 g
5 g
This item is not returnable. View return policy
577-85-5
C15H10O3
238.24
MFCD00006832
HVQAJTFOCKOKIN-UHFFFAOYSA-N
3-hydroxyflavone, flavonol, 3-hydroxy-2-phenyl-4h-chromen-4-one, flavon-3-ol, 4h-1-benzopyran-4-one, 3-hydroxy-2-phenyl, flavone, 3-hydroxy, 3-hydroxy-2-phenylchromone, unii-ztg9lss5qh, flavone,3-hydroxy, 3-hf
11349
CHEBI:5078
3-hydroxy-2-phenylchromen-4-one
OC1=C(OC2=CC=CC=C2C1=O)C1=CC=CC=C1
This item is not returnable. View return policy
577-85-5
C15H10O3
238.24
MFCD00006832
HVQAJTFOCKOKIN-UHFFFAOYSA-N
3-hydroxyflavone, flavonol, 3-hydroxy-2-phenyl-4h-chromen-4-one, flavon-3-ol, 4h-1-benzopyran-4-one, 3-hydroxy-2-phenyl, flavone, 3-hydroxy, 3-hydroxy-2-phenylchromone, unii-ztg9lss5qh, flavone,3-hydroxy, 3-hf
11349
CHEBI:5078
3-hydroxy-2-phenylchromen-4-one
OC1=C(OC2=CC=CC=C2C1=O)C1=CC=CC=C1

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.
TRUSTED_SUSTAINABILITY
Melting Point 168°C to 172°C
Quantity 1 g
Beilstein 15789
Solubility Information Insoluble in water. Soluble in N,N-DMF and ethanol.
Formula Weight 238.25
Percent Purity ≥98%
Chemical Name or Material 3-Hydroxyflavone

RUO – Research Use Only

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