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196941-73-8

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  • Benzyl 2-Acetamido-2-deoxy-3-O-(2,3,4-tri-O-benzyl-α-L-fucopyranosyl)-4,6-benzylidene-α-D-glucopyranoside

    Cas No: 196941-73-8

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196941-73-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 196941-73-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,6,9,4 and 1 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 196941-73:
(8*1)+(7*9)+(6*6)+(5*9)+(4*4)+(3*1)+(2*7)+(1*3)=188
188 % 10 = 8
So 196941-73-8 is a valid CAS Registry Number.
InChI:InChI=1/C49H53NO10/c1-33-42(52-28-35-18-8-3-9-19-35)45(53-29-36-20-10-4-11-21-36)46(54-30-37-22-12-5-13-23-37)49(57-33)60-44-41(50-34(2)51)48(55-31-38-24-14-6-15-25-38)58-40-32-56-47(59-43(40)44)39-26-16-7-17-27-39/h3-27,33,40-49H,28-32H2,1-2H3,(H,50,51)/t33?,40?,41-,42+,43+,44?,45-,46-,47?,48-,49-/m0/s1

196941-73-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzyl 2-acetamido-4,6-O-benzylidene-2-deoxy-3-O-[(5ξ)-2,3,4-tri- O-benzyl-6-deoxy-β-D-lyxo-hexopyranosyl]-α-D-threo-hexopyranoside<wbr

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:196941-73-8 SDS

196941-73-8Relevant articles and documents

Synthesis of mono- and di-α-l-fucosylated 2-acetamido-2-deoxy-N-glycyl-β-d-glucopyranosylamines, spacered fragments of glycans of N-glycoproteins

Likhosherstov,Novikova,Malysheva,Piskarev

, p. 1134 - 1141 (2016/02/09)

α-l-Fucp-(1→3)-d-GlcNAc, α-l-Fucp-(1→6)-[α-l-Fucp-(1→3)]-d-GlcNAc, and β-d-Galp-(1→3)-[α-l-Fucp-(1→4)]-d-GlcNAc were converted into corresponding β-glycopyranosylamines by action of ammonium carbamate in aqueous boric acid, or in aqueous methanol in case

Processes for the synthesis of sialyl Lewisx compounds

-

, (2008/06/13)

Disclosed are processes for the chemical synthesis of sialyl Lewisx -Y compounds where Y is --OH, --NHR, --SH, --SR or --OR, and R is an aglycon of at least one carbon atom.

An economical synthesis of Lewis X, sialyl lewis X and their α-galactosyl analogues

Dekany, Gyula,Wright, Karen,Toth, Istvan

, p. 983 - 999 (2007/10/03)

Economical syntheses of the Lewis X trisaccharide 8 and sialyl Lewis X tetrasaccharide 18 epitopes and the syntheses of the α-galactosyl epimers 9 and 20 of these structures are described. Thioglycosides 2, 5, 11 and 15 were used as glycosyl donors to con

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