210423-90-8

Basic information

• Product Name: 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-1-O-[p-(n-decanamido)benzyl]-β-D-glucopyranoside
• Synonyms: 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-1-O-[p-(n-decanamido)benzyl]-β-D-glucopyranoside
• CAS NO: 210423-90-8
• Molecular Weight: 452.461
• Mol File: 210423-90-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-1-O-[p-(n-decanamido)benzyl]-β-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-1-O-[p-(n-decanamido)benzyl]-β-D-glucopyranoside(210423-90-8)
• EPA Substance Registry System: 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-1-O-[p-(n-decanamido)benzyl]-β-D-glucopyranoside(210423-90-8)

Safety Data

• Hazardous Substances Data: 210423-90-8(Hazardous Substances Data)

Upstream product

• 158979-46-5 nitrobenzyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranoside 
• 619-73-8 4-nitrobenzyl chloride 
• 10378-06-0 2-methyl-(3,4,6-tri-O-acetyl-1,2-dideoxy-α-D-glucopyranoso)[1,2-d]-2-oxazoline 
• 3068-34-6 Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-chloro-tetrahydro-pyran-4-yl ester 

Downstream Products

• 1421930-95-1 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-1-O-(p-[(3R)-3-methoxydecanamido]benzyl)-β-D-glucopyranoside 
• 1421930-92-8 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-1-O-(p-[(3R)-3-hydroxydecanamido]benzyl)-β-D-glucopyranoside 
• 1421930-90-6 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-1-O-[p-(n-decanamido)benzyl]-β-D-glucopyranoside 
• 158979-50-1 6-Acryloylamino-hexanoic acid [4-((2R,3R,4R,5S,6R)-3-acetylamino-4,5-dihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yloxymethyl)-phenyl]-amide 
• 158979-48-7 Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-[4-(6-acryloylamino-hexanoylamino)-benzyloxy]-tetrahydro-pyran-4-yl ester 
• 158979-47-6 Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-(4-acryloylamino-benzyloxy)-tetrahydro-pyran-4-yl ester 

Relevant articles and documents

Synthesis and modification of spacered glycosides of N-acetylglucosamine

From glucosaminyl chloride peracetate, in the presence of HgI2, we have obtained β-p-nitrobenzyl-, β-ω-chloro-and β-ω-azido-spacered glycosides of N-acetylglucosamine (NAG) with spacers of different lengths and chemical natures. The correspondi

Chemoenzymatic oligosaccharide synthesis on a soluble polymeric carrier

A facile and efficient method for the chemical and enzymatic syntheses of oligosaccharides using a new type of soluble polymeric sugar acceptor substrate is described. The water soluble glycopolymers having N-acetyl-D- glucosamine (GlcNAc) branches derive