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3',4',5,7-tetra-O-acetylquercetin 3-O-(2'',3'',4'',6''-tetra-O-acetyl-β-D-glucopyranoside) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18705-98-1

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18705-98-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18705-98-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,7,0 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 18705-98:
(7*1)+(6*8)+(5*7)+(4*0)+(3*5)+(2*9)+(1*8)=131
131 % 10 = 1
So 18705-98-1 is a valid CAS Registry Number.

18705-98-1Downstream Products

18705-98-1Relevant academic research and scientific papers

Isolation and measurement of quercetin glucosides in flower buds of Japanese butterbur (Petasites japonicus subsp. gigantea Kitam.)

Matsuura, Hideyuki,Amano, Midori,Kawabata, Jun,Mizutani, Junya

, p. 1571 - 1575 (2002)

Three quercetin glucosides were isolated from flower buds of Japanese butterbur (Petasites japonicus subsp. gigantea Kitam.) together with caffeic acid as the ingredients that had DPPH radical scavenging activity, using the DPPH-HPLC method for measuring

Direct stereochemical assignmenet of hexose and pentose residues in flavonoid O-glycosides by fast atom bombardment and electrospray ionization mass spectrometry

Cuyckens, Filip,Shahat, Abdelaaty A.,Pieters, Luc,Claeys, Magda

, p. 1272 - 1279 (2007/10/03)

Mass spectrometric methods have been developed which allow the direct stereochemical assignment of terminal monosaccharide residues in flavonoid O-glycosides without the need for chemical hydrolysis. Standards containing a glucose, galactose, mannose, xylose, arabinose or apiose residue were examined because these monosaccharides are by far the most commonly encountered in flavonoid glycosides. Following acetylation, the major peracetylated sugar related fragments, generated by fast atom bombardment (FAB) or electrospray ionization (ESI), were selected for collisional activation employing a broad range of collision energies. Both FAB and ESI proved to be useful as ionization techniques. Stereoselective fragmentation was achieved and allowed us clearly to differentiate and characterize isomeric monosaccharide residues. The method developed was successfully applied to an unknown flavonoid containing a terminal pentose and hexose residue which was isolated from Farsetia aegyptia. Copyright

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