3055-46-7

Usage

Chemical Properties

White Crystalline Solid

Upstream product

• 67-56-1 methanol 
• 7512-17-6 N-Acetyl-D-glucosamine 
• 10036-64-3 N-acetyl-D-glucosamine 
• 75-36-5 acetyl chloride 
• 1078691-95-8 (+)-D-glucosamine hydrochloride 
• 72-87-7 N-acetyl-D-glucosamine 

Downstream Products

• 88295-36-7 1-O-Methyl-2-N-acetylamino-2-deoxy-4,6-O-benzyliden-α,β-D-glucopyranosid 
• 2771-48-4 methyl 2-acetamido-3,4,6-O-triacetyl-2-deoxy-β-D-glucopyranoside 
• 2595-39-3 methyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-α-D-glucopyranoside 
• 3006-60-8 Acetic acid (2R,3R,4R,5S,6R)-2,5-diacetoxy-6-acetoxymethyl-3-acetylamino-tetrahydro-pyran-4-yl ester 
• 87038-18-4 methyl 2-acetylamido-4,6-O-benzylidene-2-deoxy-β-D-glucopyranoside 
• 6619-02-9 methyl N-acetyl-2-amino-4,6-O-benzylidene-2-deoxy-α-D-glucopyranoside 
• 154125-86-7 methyl 2-deoxy-3,4,6-tri-O-benzyl-2-(N-acetylamino)-α-D-glucopyranoside 
• 375824-36-5 methyl 2-acetamido-2-deoxy-6-O-p-tolylsulfonyl-β-D-glucopyranoside 
• 53756-24-4 ((2R,3S,4R,5R,6S)-5-acetamido-3,4-dihydroxy-6-methoxytetrahydro-2H-pyran-2-yl)methyl 4-methylbenzenesulfonate 
• 1370587-63-5 methyl 2-acetamido-3,6-di-O-benzoyl-2-deoxy-β-D-xylo-hexapyranoside-4-ulose 
• 1370586-83-6 methyl 2-acetamido-3,6-di-O-benzoyl-2-deoxy-α-D-xylo-hexapyranosid-4-ulose 
• 1370586-92-7 methyl 2-acetamido-3,4,6-tri-O-benzoyl-2-deoxy-α-D-glucopyranoside 
• 176690-90-7 methyl 2-acetamido-3,6-di-O-benzoyl-2-deoxy-β-D-glucopyranoside 
• 269065-36-3 methyl 2-acetamido-3,6-di-O-benzoyl-2-deoxy-α-D-glucopyranoside 

Relevant academic research and scientific papers

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Synthetic development of sugar amino acid oligomers towards novel podophyllotoxin analogues

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Ultrasonication-Assisted Synthesis of a d-Glucosamine-Based β-CD Inclusion Complex and Its Application as an Aqueous Heterogeneous Organocatalytic System

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Ring-Opening Reactions of the N-4-Nosyl Hough-Richardson Aziridine with Nitrogen Nucleophiles

Dinosylated α-d-glucopyranoside was directly transformed into α-d-altropyranosides via in situ formed N-4-nosyl Hough-Richardson aziridine with nitrogen nucleophiles under mild conditions in fair to excellent yields. The scope of the aziridine ring-opening reaction was substantially broadened contrary to the conventional methods introducing solely the azide anion at high temperatures. If necessary, the N-4-nosyl Hough-Richardson aziridine can be isolated by filtration in a very good yield and high purity.

N-acetylgalactosamine green synthetic method

The present invention discloses a N-acetylgalactosamine green synthetic method. According to the method, N-acetylglucosamine as a raw material is successively condensed with an alcohol and pivaloyl chloride, and then N-acetylgalactosamine can be obtained

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Synthetic heparin pentasaccharides

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Glucosamine-based primary amines as organocatalysts for the asymmetric aldol reaction

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Oligo-Aminosaccharide compound

An oligo-aminosaccharide compound formed by binding 3 to 6 saccharides, such as 2,6-diamino-2,6-dideoxy-α-(1→4)-D-glucopyranose oligomers, or a salt thereof, which has high affinity to a double-stranded nucleic acid.

Synthesis and characterization of d-glucosamine-derived low molecular weight gelators

Carbohydrate-based low molecular weight gelators are an interesting class of molecules with many potential applications. Previously, we have found that certain esters and carbamates of 4,6-O-benzylidene-α-d-methyl- glucopyranoside are low molecular weight