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1,6-Anhydro-2,3-di-O-benzyl-β-D-galactopyranose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

61074-29-1

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61074-29-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 61074-29-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,0,7 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 61074-29:
(7*6)+(6*1)+(5*0)+(4*7)+(3*4)+(2*2)+(1*9)=101
101 % 10 = 1
So 61074-29-1 is a valid CAS Registry Number.

61074-29-1Downstream Products

61074-29-1Relevant academic research and scientific papers

SYNTHESIS OF 1,6-ANHYDRO-2,3-DI-O-FARNESYL-5-O-(PHOSPHINYL>METHYL)-α-D-GALACTOFURANOSE: A ZARAGOZIC ACID - PRESQUALENE PYROPHOSPHATE HYBRID

Valentijn, A. R. P. M.,Broxterman, H. J. G.,Marel, G. A. van der,Cohen, L. H.,Boom, J. H. van

, p. 737 - 750 (2007/10/02)

A multi-step synthesis of a new potential inhibitor (i.e., compound 2) of squalene synthase is described, starting from D-galactose.The title compound is a hybrid of presqualene pyrophosphate and the recently discovered zaragozic acids, which are picomola

α-Glucosidase Inhibitors, 6. - Synthesis of 1,6-Anhydro-D-glucose and -D-galactose Derivatives - Preparation of 1-Deoxynojirimycin

Schmidt, Richard R.,Michel, Josef,Ruecker, Ernst

, p. 423 - 428 (2007/10/02)

Methyl 2,3-di-O-benzyl-D-glucopyranoside (2) is transformed in the presence of p-toluenesulfonic acid and 2,2,2-trichloro- or 2,2,2-trifluoroethanol into the 4-O-unprotected 1,6-anhydropyranose 4.The amount of 1,6-anhydrofuranose 5, formed as a byproduct of this reaction, can be increased by longer reaction times.Similarly, from methyl 2,3-di-O-benzyl-D-galactopyranoside (9) the corresponding 1,6-anhydro compounds 10 and 12 were obtained. 1-Deoxynojirimycin (31) is obtained from the 5-O-unprotected 1,6-anhydroglucofuranose 5 in a few steps.The stereoselectiveintroduction of nitrogen at C-5 is reached by inversion of the configuration of the 5-OH group through oxidation and reduction and subsequent triflate activation for the invertive azide group introduction

Bausteine von Oligosacchariden, XXXII. Synthese der verzweigten Pentasaccharid-Einheit der O-spezifischen Seitenkette des Lipopolysaccharides von Shigella Dysenteriae

Paulsen, Hans,Buensch, Hellmut

, p. 3126 - 3145 (2007/10/02)

The branched pentasaccharide sequence 43 was synthesized.This is the repeating-unit of the O-specific side chain belonging to the lipopolysaccharide obtained from Shigella Dysenteriae of serotype two.A trisaccharide halide block, obtained from three 2-azi

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