54542-51-7

Basic information

• Product Name: QUERCETIN-3-O-BETA-D-GLUCOPYRANOSYL-6''-ACETATE
• Synonyms: QUERCETIN-3-O-B-D-GLUCOPYRANOSYL-6''-ACETATE;QUERCETIN-3-O-BETA-D-GLUCOPYRANOSYL-6''-ACETATE;QUERCETIN-3-O-D-GLUCOPYRANOSYL-6''-ACETATE;QUERCETIN-3-O-GLUCOSE-6''-ACETATE;6"-O-Acetylisoquercitrin
• CAS NO: 54542-51-7
• Molecular Formula: C₂₃H₂₂O₁₃
• Molecular Weight: 506.41
• Product Categories: Penta-substituted Flavones
• Mol File: 54542-51-7.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 848.3±65.0 °C(Predicted)
• Appearance: /
• Density: 1.77±0.1 g/cm3(Predicted)
• PKA: 6.17±0.40(Predicted)
• CAS DataBase Reference: QUERCETIN-3-O-BETA-D-GLUCOPYRANOSYL-6''-ACETATE(CAS DataBase Reference)
• NIST Chemistry Reference: QUERCETIN-3-O-BETA-D-GLUCOPYRANOSYL-6''-ACETATE(54542-51-7)
• EPA Substance Registry System: QUERCETIN-3-O-BETA-D-GLUCOPYRANOSYL-6''-ACETATE(54542-51-7)

Safety Data

• Hazardous Substances Data: 54542-51-7(Hazardous Substances Data)

Usage

General Description

QUERCETIN-3-O-BETA-D-GLUCOPYRANOSYL-6''-ACETATE is a chemical compound that belongs to the flavonoid group and is derived from plants. It is a glycoside, meaning it has a sugar molecule attached to it, and it contains the flavonol quercetin as its aglycone. QUERCETIN-3-O-BETA-D-GLUCOPYRANOSYL-6''-ACETATE has been studied for its potential health benefits, including its antioxidant and anti-inflammatory properties. It has also been investigated for its potential role in cancer prevention and treatment, as well as in the management of cardiovascular and neurodegenerative diseases. QUERCETIN-3-O-BETA-D-GLUCOPYRANOSYL-6''-ACETATE is commonly found in various fruits, vegetables, and herbs, and it is available as a dietary supplement for its potential health-promoting effects.

Upstream product

• 482-35-9 isoquercetin 
• 64-19-7 acetic acid 
• 108-05-4 vinyl acetate 
• 96862-01-0 quercetin 3-O-(6′′-O-malonyl)-β-glucopyranoside 

Downstream Products

• 18705-98-1 3',4',5,7-tetra-O-acetylquercetin 3-O-(2'',3'',4'',6''-tetra-O-acetyl-β-D-glucopyranoside) 

Relevant articles and documents

Isoquercitrin esters with mono- or dicarboxylic acids: Enzymatic preparation and properties

A series of isoquercitrin (quercetin-3-O-β-D-glucopyranoside) esters with mono- or dicarboxylic acids was designed to modulate hydro- and lipophilicity and biological properties. Esterification of isoquercitrin was accomplished by direct chemoenzymatic re

DECARBOXYLATION AND EXCHANGE REACTIONS IN FLAVONOID GLYCOSIDE MALONATES

Flavonoid malonylglycosides lose carbon dioxide and give the corresponding flavonoid acetylglycosides under conditions that are often used in determining their NMR spectra (DMSO-d6 at 80-100 deg C).If the solvent contains exchangeable deuterium the malonyl methylene protons may exchange and trideuterioacetyl derivatives form.The NMR spectra of these substances should be run initially at ambient temperature in the absence of solvents containing exchangeable deuterium.Key Word Index - Gerbera jamesonii; Compositae; Ipomoea tricolor; Convolvulaceae; NMR; decarboxylation; proton-deuterium exchange; flavonoid malonylglycosides.