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(2S,3R,4S,5S,6R)-2-(((2R,3S,4R,5R,6S)-4-acetoxy-2-(acetoxymethyl)-5-azido-6-((tertbutyldiphenylsilyl)oxy)tetrahydro-2H-pyran-3-yl)oxy)-6-(acetoxymethyl)tetrahydro-2H-pyran-3,4,5-triyl triacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

213591-31-2

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213591-31-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 213591-31-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,5,9 and 1 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 213591-31:
(8*2)+(7*1)+(6*3)+(5*5)+(4*9)+(3*1)+(2*3)+(1*1)=112
112 % 10 = 2
So 213591-31-2 is a valid CAS Registry Number.

213591-31-2Relevant academic research and scientific papers

One-Step TEMPO-Catalyzed and Water-Mediated Stereoselective Conversion of Glycals into 2-Azido-2-deoxysugars with a PIFA-Trimethylsilyl Azide Reagent System

Chennaiah, Ande,Vankar, Yashwant D.

supporting information, p. 2611 - 2614 (2018/05/17)

An unprecedented water-mediated and TEMPO-catalyzed, one-step, highly regiospecific and stereoselective functionalization of glycals to 2-azido-2-deoxysugars has been developed using a PIFA-Me3SiN3 reagent system in the presence of B

Synthesis of Neolacto ganglioside LM1

Tietze, Lutz F.,Janssen, Christian O.,Gewert, Jan-Arne

, p. 1887 - 1894 (2007/10/03)

The synthesis of the ganglioside LM1 (1) has been performed by glycosidation of 2 with azidosphingosine 3, followed by reduction of the azido group, acylation with stearine anhydride (4), and solvolysis. 2 was obtained from sialyl xanthate 5 and tetrasacc

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