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4',7-di-O-benzyl-3-O-(β-D-glucopyranosyl)quercetin is a complex organic compound derived from quercetin, a naturally occurring flavonoid found in various fruits, vegetables, and herbs. This specific derivative features two benzyl groups attached to the 4' and 7 positions of the quercetin molecule, and a β-D-glucopyranosyl group linked to the 3 position. The benzyl groups are phenylmethyl moieties that contribute to the compound's lipophilicity, potentially enhancing its bioavailability and stability. The β-D-glucopyranosyl group is a sugar molecule that can influence the compound's solubility and interaction with biological systems. This chemical modification of quercetin is often pursued for pharmaceutical or research purposes to study the effects of these structural changes on the molecule's biological activity, such as its antioxidant properties or potential therapeutic applications.

6743-87-9

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6743-87-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6743-87-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,4 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6743-87:
(6*6)+(5*7)+(4*4)+(3*3)+(2*8)+(1*7)=119
119 % 10 = 9
So 6743-87-9 is a valid CAS Registry Number.

6743-87-9Downstream Products

6743-87-9Relevant academic research and scientific papers

Synthesis of quercetin 3-O-[6"-O-(trans-p-coumaroyl)]-β-D- Glucopyranoside

Ren, Xuhong,Shen, Liu-Lan,Muraoka, Osamu,Cheng, Maosheng

, p. 119 - 131 (2012/01/13)

This report describes the efficient synthesis of quercetin 3-O-[6"-O-(trans-pcoumaroyl)]- β-D-glucopyranoside 1 (isoquercitrin coumarate), an acylated quercetin glycoside possessing antihypertensive, antidiabetic, and tyrosinase inhibitory activities. The synthesis is initiated from commercially available quercetin via regioselective benzylation of quercetin to produce 4', 7-di-O-benzylquercetin (4). Through 4, 1 was successfully achieved via selective β-glycosylation of the 3-OH, acylation of 6"-OH, and finally debenzylation via catalytic transfer hydrogenation. Taylor & Francis Group, LLC.

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