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(E)-3'-Methoxy-2',3,4,4'-tetrahydroxychalcone is a naturally occurring flavonoid compound characterized by its unique chemical structure. It is a chalcone derivative, which means it is a type of flavonoid with an open-chain structure. This particular compound is distinguished by the presence of four hydroxyl groups (-OH) at positions 2', 3, 4, and 4', and a methoxy group (-OCH3) at the 3' position. These functional groups contribute to its antioxidant properties, which are beneficial for health. The compound is found in various plants and has been studied for its potential therapeutic effects, including anti-inflammatory and anticancer activities. Its chemical structure and biological activities make it a subject of interest in the field of natural product chemistry and pharmacology.

6542-59-2

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6542-59-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6542-59-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,4 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6542-59:
(6*6)+(5*5)+(4*4)+(3*2)+(2*5)+(1*9)=102
102 % 10 = 2
So 6542-59-2 is a valid CAS Registry Number.

6542-59-2Upstream product

6542-59-2Downstream Products

6542-59-2Relevant academic research and scientific papers

Convenient synthesis and physiological activities of flavonoids in Coreopsis lanceolata L. petals and their related compounds

Nakabo, Daisuke,Okano, Yuka,Kandori, Naomi,Satahira, Taisei,Kataoka, Naoya,Akamatsu, Junpei,Okada, Yoshiharu

, p. 1 - 25 (2018)

Chalcones, flavanones, and flavonols, including 8-methoxybutin isolated from Coreopsis lanceolata L. petals, were successfully synthesized with total yields of 2–59% from O-methylpyrogallols using the Horner–Wadsworth–Emmons reaction as a key reaction. Au

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