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O-(4-O-acetyl-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-(1->4)-3,6-di-O-benzyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl azide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

161315-67-9

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161315-67-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 161315-67-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,3,1 and 5 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 161315-67:
(8*1)+(7*6)+(6*1)+(5*3)+(4*1)+(3*5)+(2*6)+(1*7)=109
109 % 10 = 9
So 161315-67-9 is a valid CAS Registry Number.

161315-67-9Relevant academic research and scientific papers

Chemoselective ligation applied to the synthesis of a biantennary N-linked glycoform of CD52

Pratt, Matthew R.,Bertozzi, Carolyn R.

, p. 6149 - 6159 (2007/10/03)

We report here a strategy for the synthesis of N-linked glycopeptide analogues that replace the glycosidic linkages extending from the core pentasaccharide with thioethers amenable to construction by chemoselective ligation. The key building block, a pent

Synthesis of a core trisaccharide as a versatile building block for N-glycans and glycoconjugates

Unverzagt, Carlo

, p. 1369 - 1376 (2007/10/03)

N-Linked oligosaccharides from glycoproteins (N-glycans) can be conveniently assembled with a building block approach. A protected form of the core trisaccharide (β-mannosyl chitobiose) was identified as a key building block. The chitobiose part of the co

A new strategy for the synthesis of the core trisaccharide of asparagine-linked sugar chains

Matsuo, Ichiro,Isomura, Megumi,Walton, Richard,Ajisaka, Katsumi

, p. 8795 - 8798 (2007/10/03)

The core trisaccharide common to all asparagine-linked glycoprotein olisosaccharides was synthesized using two novel processes: 1) regioselective acetylation using lipase, and 2) inversion of the C-2 hydroxyl group of the glucose residue in a glucosyl chi

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