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

290330-40-4

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290330-40-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 290330-40-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,0,3,3 and 0 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 290330-40:
(8*2)+(7*9)+(6*0)+(5*3)+(4*3)+(3*0)+(2*4)+(1*0)=114
114 % 10 = 4
So 290330-40-4 is a valid CAS Registry Number.

290330-40-4Downstream Products

290330-40-4Relevant academic research and scientific papers

Highly regioselective synthesis of a 3-O-sulfonated arabino Lewisa asparagine building block suitable for glycopeptide synthesis

Roesch, Alexander,Kunz, Horst

, p. 1597 - 1608 (2007/10/03)

Using the stannylene method, the trisaccharide 2-acetamido-3-O-[6-O-benzyl-β-d-galactopyranosyl]-4-O-[2,3,4-tri-O-benzyl-β-d-arabinopyranosyl]-6-O-benzyl-2-deoxy-β-d-glucopyranosyl azide was regioselectively sulfonated and, after reduction of the anomeric

A Sialyl-Lewis A-asparagine building block for glycopeptide-synthesis

Peilst?cker, Karen,Kunz, Horst

, p. 820 - 822 (2007/10/03)

Using the azido group as the anomeric protection a Sialyl Lewis A tetrasaccharide was synthesized from N-acetylglucosamine via the type1 lactosamine and Lewis A intermediates. After reduction of the azido group, coupling with Fmoc α-allyl aspartate and Pd

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