3055-51-4

Basic information

• Product Name: BENZYL 2-ACETAMIDO-2-DEOXY-§-D-GLUCOPYRANOSIDE
• Synonyms: BENZYL 2-ACETAMIDO-2-DEOXY-§-D-GLUCOPYRANOSIDE
• CAS NO: 3055-51-4
• Molecular Formula: C₁₅H₂₁NO₆
• Molecular Weight: 311.33
• Mol File: 3055-51-4.mol
• Article Data: 37

Chemical Properties

• Melting Point: 183 °C
• Boiling Point: 594.9±50.0 °C(Predicted)
• Appearance: /
• Density: 1.34±0.1 g/cm3(Predicted)
• PKA: 12.98±0.70(Predicted)
• CAS DataBase Reference: BENZYL 2-ACETAMIDO-2-DEOXY-§-D-GLUCOPYRANOSIDE(CAS DataBase Reference)
• NIST Chemistry Reference: BENZYL 2-ACETAMIDO-2-DEOXY-§-D-GLUCOPYRANOSIDE(3055-51-4)
• EPA Substance Registry System: BENZYL 2-ACETAMIDO-2-DEOXY-§-D-GLUCOPYRANOSIDE(3055-51-4)

Safety Data

• Hazardous Substances Data: 3055-51-4(Hazardous Substances Data)

Upstream product

• 117177-19-2 2-methyl-(1,2-dideoxy-5,6-O-isopropylidene-α-D-glucofurano)-<2,1-d>-2-oxazoline 
• 100-51-6 benzyl alcohol 
• 1040191-33-0 N'-(2-acetamido-2-deoxy-β-D-glucopyranosyl)-p-toluenesulfono-hydrazide 
• 7512-17-6 N-Acetyl-D-glucosamine 
• 1078691-95-8 (+)-D-glucosamine hydrochloride 
• 100-39-0 benzyl bromide 
• 10036-64-3 N-acetyl-D-glucosamine 
• 74034-09-6 2-acetamido-1,5-anhydro-4,6-O-benzylidene-2-deoxy-D-glucitol 
• 4710-88-7 3,4,6-tri-O-acetyl-2-amino-2-deoxy-α-D-glucopyranosyl bromide hydrobromide 
• 62098-31-1 benzyl 3,4,6-tri-O-acetyl-2-amino-2-deoxy-β-D-glucopyranoside 
• 3068-34-6 Acetic acid (2R,3S,4R,5R,6R)-3-acetoxy-2-acetoxymethyl-5-acetylamino-6-chloro-tetrahydro-pyran-4-yl ester 
• 3006-60-8 2-acetamido-1,3,4,6-tetra-O-acetyl-2-deoxy-β-D-glucopyranose 
• 51533-00-7 2-acetylamino-3,4,6-triacetyl-2-deoxy-α-D-glucopyranosyl bromide 
• 5432-46-2 1,3,4,6-tetra-O-acetyl-D-glucosamine hydrochloride 

Downstream Products

• 40656-45-9 benzyl 2-acetamido-6-bromo-2,6-dideoxy-α-D-glucopyranoside 
• 13343-63-0 benzyl 4,6-O-benzylidene-2-acetylamino-2-deoxy-α-D-glucopyranoside 
• 120903-68-6 N-[(2S,3R,4R,5S,6R)-2-Benzyloxy-6-(tert-butyl-dimethyl-silanyloxymethyl)-4,5-dihydroxy-tetrahydro-pyran-3-yl]-acetamide 
• 176167-78-5 benzyl 2-acetamido-3,6-di-O-benzoyl-β-D-allopyranoside 
• 13320-00-8 benzyl 2-acetamido-3-O-acetyl-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside 
• 189683-17-8 Acetic acid (2S,3S,4R,5R,6S)-4,5-diacetoxy-2-((2R,3S,4R,5R,6R)-3-acetylamino-2-benzyloxy-5-hydroxy-6-hydroxymethyl-tetrahydro-pyran-4-ylsulfanyl)-6-methyl-tetrahydro-pyran-3-yl ester 
• 19374-64-2 N-((4aR,6R,7R,8S,8aS)-6-Benzyloxy-8-hydroxy-2-phenyl-hexahydro-pyrano[3,2-d][1,3]dioxin-7-yl)-acetamide 
• 14040-20-1 benzyl 2-acetamido-3-O-benzyl-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside 
• 62867-63-4 benzyl 2-acetamido-2-deoxy-3,6-di-O-benzyl-β-D-glucopyranoside 
• 62867-64-5 benzyl 2-acetamido-4-O-(2-O-acetyl-3,4,6-tri-O-benzyl-β-D-glucopyranosyl)-3,6-di-O-benzyl-2-deoxy-β-D-glucopyranoside 
• 120903-74-4 N-Benzyl-N-((1S,2R,3S,6S)-2,3-bis-benzyloxy-6-hydroxy-4-oxo-cyclohexyl)-acetamide 
• 120903-73-3 N-Benzyl-N-((2S,3R,4R,5S)-2,4,5-tris-benzyloxy-6-methylene-tetrahydro-pyran-3-yl)-acetamide 
• 120903-72-2 N-Benzyl-N-((2S,3R,4R,5S,6S)-2,4,5-tris-benzyloxy-6-iodomethyl-tetrahydro-pyran-3-yl)-acetamide 

Relevant articles and documents

Synthesis of Bacterial-Derived Peptidoglycan Cross-Linked Fragments

Peptidoglycan (PG) is the core structural motif of the bacterial cell wall. Fragments released from the PG serve as fundamental recognition elements for the immune system. The structure of the PG, however, encompasses a variety of chemical modifications among different bacterial species. Here, the applicability of organic synthetic methods to address this chemical diversity is explored, and the synthesis of cross-linked PG fragments, carrying biologically relevant amino acid modifications and peptide cross-linkages, is presented using solution and solid phase approaches.

Synthesis of lipo-chitooligosaccharide analogues and their interaction with LYR3, a high affinity binding protein for Nod factors and Myc-LCOs

Lipo-chitotetrasaccharide analogues where one central GlcNAc residue was replaced by a triazole unit have been synthesized from a derivative obtained by chitin depolymerization and a functionalized N-acetyl-glucosamine via the copper-catalyzed azide-alkyn

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6-Sulfo-6-deoxy-D-glucosamine (GlcN6S), 6-sulfo-6-deoxy-D-glucosaminitol (ADGS) and their N-acetyl and methyl ester derivatives have been synthesized and tested as inhibitors of enzymes catalyzing reactions of the UDP-GlcNAc pathway in bacteria and yeasts