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5-azidopentyl (2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-galactopyranosyl)-(1->4)-(2,6-di-O-benzyl-3-O-p-methoxybenzyl-β-D-galactopyranosyl)-(1->4)-2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

190247-79-1

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  • 5-azidopentyl (2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-galactopyranosyl)-(1->4)-(2,6-di-O-benzyl-3-O-p-methoxybenzyl-β-D-galactopyranosyl)-(1->4)-2-acetamido-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside

    Cas No: 190247-79-1

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190247-79-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 190247-79-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,0,2,4 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 190247-79:
(8*1)+(7*9)+(6*0)+(5*2)+(4*4)+(3*7)+(2*7)+(1*9)=141
141 % 10 = 1
So 190247-79-1 is a valid CAS Registry Number.

190247-79-1Upstream product

190247-79-1Relevant articles and documents

Synthesis of two analogues of the Sda determinant. Replacement of the sialic acid residue by a sulfate or a carboxymethyl group.

van Seeventer,Corsten,Sanders,Kamerling,Vliegenthart

, p. 171 - 179 (1997)

Two analogues of the Sda determinant tetrasaccharide have been synthesized in order to investigate the physiological role of this carbohydrate moiety. These saccharides, having two different anionic substitutes for the sialic acid residue, are: beta-D-GalpNAc-(1-->4)-3-O-SO3 H- beta-D-Galp-(1-->4)-beta-D-GlcpNAc-(1-->O)(CH2)5NH2 and beta-D-GalpNAc-(1-->4)-3-O- COOH-beta-D-Galp-(1-->4)-beta-D-GlcpNAc-(1-->O)(CH2)5NH2. 5-Azidopentyl (2,6-di-O- benzyl-beta-D-galactopyranosyl)-(1-->4)-3,6-di-O-benzyl-2-deoxy-2- phthalimido-beta-D-glucopyranoside served as a general building block. The trisaccharides were obtained after prior selective derivatization of HO-3' of the disaccharide derivative via a dibutyltin oxide mediated reaction, followed by coupling at HO-4' with 3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-beta-D-galactopyranosyl trichloroacetimidate, and processing of the formed trisaccharide derivatives into their free forms.

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