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(3-trifluoroacetamidopropyl)-2-acetamido-3-O-acetyl-6-O-benzyl-2-deoxy-4-O-{2,4-di-O-acetyl-6-O-benzyl-3-O-[2-acetamido-3-O-acetyl-6-O-benzyl-2-deoxy-4-O-(2,3,4-tri-O-acetyl-6-O-benzyl-β-D-galactopyranosyl)-β-D-glucopyranosyl]-β-D-galactopyranosyl}-β-D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1155352-43-4

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1155352-43-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1155352-43-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,5,3,5 and 2 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1155352-43:
(9*1)+(8*1)+(7*5)+(6*5)+(5*3)+(4*5)+(3*2)+(2*4)+(1*3)=134
134 % 10 = 4
So 1155352-43-4 is a valid CAS Registry Number.

1155352-43-4Downstream Products

1155352-43-4Relevant academic research and scientific papers

The synthesis of linear trilactosamine

Pazynina,Severov,Bovin

experimental part, p. 625 - 631 (2009/04/11)

TrilactosamineGalβ1-4GlcNAcβ1-3Galβ1-4GlcNAcβ1- 3Galβ1-4GlcNAcβ-sp, where sp = O(CH2)3NH 2 is a spacer, was synthesized. The tetrasaccharide fragment Galβ1-4GlcNAcβ1-3Galβ1-4GlcNAcβ-sp was obtained by successive glycosylation using elongation by one monosaccharide residue at a time; and the tetrasaccharide was then transformed into a hexasaccharide with a disaccharide glycosyl donor. A 2,2,2-trichloroethoxycarbonyl group was used for the protection of the glucosamine amino group.

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