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2′-Hydroxy-3′-methoxyflavone is a naturally occurring flavonoid compound characterized by the presence of a hydroxyl group at the 2′ position and a methoxy group at the 3′ position on its flavone backbone. Flavonoids are a class of polyphenolic compounds widely found in plants, and they are known for their diverse biological activities, including antioxidant, anti-inflammatory, and anticancer properties. 2′-Hydroxy-3′-methoxyflavone, in particular, has been studied for its potential health benefits, such as its ability to modulate cellular signaling pathways and protect against oxidative stress. 2′-hydroxy-3′-methoxyflavone is typically extracted from plant sources and can be found in various parts of plants, including leaves, flowers, and fruits. Its chemical structure and biological activities make it a subject of interest in the fields of pharmacology and nutrition.

2570-32-3

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2570-32-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2570-32-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,7 and 0 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2570-32:
(6*2)+(5*5)+(4*7)+(3*0)+(2*3)+(1*2)=73
73 % 10 = 3
So 2570-32-3 is a valid CAS Registry Number.

2570-32-3Downstream Products

2570-32-3Relevant academic research and scientific papers

Synthesis and anti-platelet, anti-inflammatory and anti- allergic activities of methoxyisoflavanquinone and related compounds

Chang, Chiung-Yun,Huang, Li-Jiau,Wang, Jih-Pyang,Teng, Che-Ming,Chen, Sheng-Chih,Kuo, Sheng-Chu

, p. 964 - 973 (2007/10/03)

In a continuation of our search for novel anti-platelet agents, isoflavone quinone and isoflavanquinone were selected as lead compounds and the synthesis of their methoxy derivatives was carried out. Among them, the 4'- and 7-methoxy derivatives were successfully prepared, whereas the attempt to obtain 3'-methoxy derivatives resulted in their isomers, 3'-methoxyflavone quinone and 3'-methoxyflavanquinone, instead. After screening for their anti-platelet, anti-inflammatory and anti-allergic activities, a preliminary structure-activity relationship was established. Compounds 6c, 7a - c, 8c and 9a - c were found to exhibit significant activities. In particular, compound 7c demonstrated very potent anti-platelet, anti-inflammatory and anti-allergic activities and was then recommended for further pharmacological investigation.

Regiospecific demethylation-sulfonation of 2',3'-dimethoxyflavones

Habsaoui, Amar,Cami, Jose Luis Franquet,Wallet, Jean Claude,Gaydou, Emile M.

, p. 1759 - 1767 (2007/10/03)

By a careful control of the temperature at 85°C, the selective demethylation of 2',3'-dimethoxyflavones with sulfuric acid occurs at the 2'-hindered methoxy group followed by para sulfonation. At higher temperature, demethylation is complete.

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