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Methyl 2,3,6,2',3',6'-hexa-O-benzyl-β-D-maltoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

19474-57-8

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19474-57-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19474-57-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,4,7 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 19474-57:
(7*1)+(6*9)+(5*4)+(4*7)+(3*4)+(2*5)+(1*7)=138
138 % 10 = 8
So 19474-57-8 is a valid CAS Registry Number.

19474-57-8Downstream Products

19474-57-8Relevant academic research and scientific papers

An efficient glycosylation reaction for the synthesis of asialo GM2 analogues

Sun, Bin,Pukin, Aliaksei V.,Visser, Gerben M.,Zuilhof, Han

, p. 7371 - 7374 (2007/10/03)

We investigated the coupling reaction of glycosyl donors N-trichloroethoxycarbonyl-galactosamine-O-trichloroacetimidate (2a) and N-p-nitrobenzyloxycarbonyl-galactosamine-O-trichloroacetimidate (2b) with the 4′-OH of lactose derivatives (3a-d) to synthesiz

SN2 displacement of carbohydrate triflates by 9-oximes of erythromycin a and of a tylosin derivative

Grandjean, Cyrille,Lukacs, Gabor

, p. 831 - 855 (2007/10/03)

The preparation of 9-O-glycosyloxime derivatives of erythromycin A (1) and tylosin (2) is reported. Access to this new class of macrolides was achieved from (E)-9-oxime of erythromycin A (3) and 9-oxime of tylosin 20-(1,3-dithiane) (4), by successful disp

Studies of the molecular recognition of synthetic methyl β-lactoside analogues by Ricinus communis agglutinin

Rivera-Sagredo,Jimenez-Barbero,Martin-Lomas,Solis,Diaz-Maurino

, p. 207 - 226 (2007/10/02)

The 2-, 3-, 6-, 2'-, 3'-, 4'-, and 6'-deoxy derivatives and the 3-O-methyl derivative of methyl β-lactoside have been synthesised and their binding to the galactose-specific agglutinin from Ricinus communis (RCA-120) has been investigated. The results ind

The substrate specificity of the enzyme amyloglucosidase (AMG). Part I. Deoxy derivatives.

Bock,Pedersen

, p. 617 - 628 (2007/10/02)

The eight possible monodeoxy derivatives of methyl beta-maltoside and two bisdeoxy derivatives have been synthesized. The unprotected glycosides have all been investigated by NMR (1H and 13C) spectroscopy in order to confirm their structures and to obtain

SYNTHESIS OF DI-, TRI-, AND TETRA-SACCHARIDES CORRESPONDING TO RECEPTOR STRUCTURES RECOGNISED BY Streptococcus pneumoniae

Dahmen, Jan,Gnosspelius, Goesta,Larsson, Ann-Charlott,Lave, Thomas,Noori, Ghazi,et al.

, p. 17 - 28 (2007/10/02)

Syntheses are described for methyl 2-acetamido-2-deoxy-4-O-β-D-galactopyranosyl-α-D-glucopyranoside, methyl 2-acetamido-2-deoxy-4-O-β-D-galactopyranosyl-β-D-glucopyranoside, methyl 3-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-β-D-galactopyranoside, methyl

SYNTHESIS OF THE TRISACCHARIDE MOIETY OF GANGLIOTRIOSYLCERAMIDE (ASIALO GM2)

Wessel, Hans-Peter,Iversen, Tommy,Bundle, David R.

, p. 5 - 22 (2007/10/02)

The synthesis of the trisaccharide methyl glycoside β-D-GalNAc-(1->4)-β-D-Gal-(1->4)-β-D-Glc-OMe, which corresponds to the carbohydrate portion of gangliotriosylceramide (asialo GM2), was accomplished by the reaction of 4-O-acetyl-3,6-di-O-benz

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