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139459-55-5

139459-55-5

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  • 4-Nitrophenyl 2-acetamido-6-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-3-O-(β-D-galactopyranosyl)-2-deoxy-α-D-galactopyranoside

    Cas No: 139459-55-5

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  • 4-Nitrophenyl 2-Acetamido-6-O-(2-acetamido-2-deoxy-b-D-glucopyranosyl) -3-O-(b-D-galactopyranosyl)-2-deoxy-a- D-galactopyranoside

    Cas No: 139459-55-5

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  • 4-Nitrophenyl 2-Acetamido-6-O-(2-acetamido-2-deoxy-b-D-glucopyranosyl) -3-O-(b-D-galactopyranosyl)-2-deoxy-a-D-galactopyranoside

    Cas No: 139459-55-5

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139459-55-5 Usage

Chemical Properties

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4-Nitrophenyl 2-Acetamido-6-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl) -3-O-(β-D-galactopyranosyl)-2-deoxy-α-D-galactopyranoside (cas# 139459-55-5) is a compound useful in organic synthesis.

Check Digit Verification of cas no

The CAS Registry Mumber 139459-55-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,9,4,5 and 9 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 139459-55:
(8*1)+(7*3)+(6*9)+(5*4)+(4*5)+(3*9)+(2*5)+(1*5)=165
165 % 10 = 5
So 139459-55-5 is a valid CAS Registry Number.
InChI:InChI=1/C28H41N3O18/c1-10(34)29-17-22(39)19(36)14(7-32)46-26(17)44-9-16-21(38)25(49-28-24(41)23(40)20(37)15(8-33)47-28)18(30-11(2)35)27(48-16)45-13-5-3-12(4-6-13)31(42)43/h3-6,14-28,32-33,36-41H,7-9H2,1-2H3,(H,29,34)(H,30,35)

139459-55-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Nitrophenyl 2-acetamido-6-O-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-3-O-(β-D-galactopyranosyl)-2-deoxy-α-D-galactopyranoside

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

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More Details:139459-55-5 SDS

139459-55-5Relevant articles and documents

Synthesis of mucin O-glycan core structures as their p-nitro- and p-aminophenyl glycosides

Hollinger, Martin,Abraha, Fana,Oscarson, Stefan

experimental part, p. 1454 - 1466 (2011/08/22)

For the investigation of glycosidases, and for the construction of glycan arrays the p-nitrophenyl- and p-aminophenyl glycosides of mucin O-glycan core structures 1-7 and the 2,6-ST-antigen have been chemically synthesized using d-galactose as a precursor for GalNAc residues. GlcNAc residues have partly been introduced using a 4,6-di-O-benzoyl-2,3-N,O-oxazolidinone-protected donor, which allowed deprotection of the formed di- and tri-saccharides in one step using sodium methoxide.

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