154125-86-7

Basic information

• Product Name: methyl 2-deoxy-3,4,6-tri-O-benzyl-2-(N-acetylamino)-α-D-glucopyranoside
• Synonyms: methyl 2-deoxy-3,4,6-tri-O-benzyl-2-(N-acetylamino)-α-D-glucopyranoside
• CAS NO: 154125-86-7
• Molecular Weight: 505.611
• Mol File: 154125-86-7.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: methyl 2-deoxy-3,4,6-tri-O-benzyl-2-(N-acetylamino)-α-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2-deoxy-3,4,6-tri-O-benzyl-2-(N-acetylamino)-α-D-glucopyranoside(154125-86-7)
• EPA Substance Registry System: methyl 2-deoxy-3,4,6-tri-O-benzyl-2-(N-acetylamino)-α-D-glucopyranoside(154125-86-7)

Safety Data

• Hazardous Substances Data: 154125-86-7(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 154125-89-0 2-acetamido-1,5-anhydro-1-azi-3,4,6-tri-O-benzyl-2-deoxy-D-glucitol 
• 100-44-7 benzyl chloride 
• 6082-04-8 methyl 2-acetylamido-2-deoxy-D-glucoside 
• 100-39-0 benzyl bromide 
• 3055-46-7 methyl N-acetyl-D-glucosamine 
• 7512-17-6 N-Acetyl-D-glucosamine 

Downstream Products

• 1262427-24-6 methyl 3,4,6-O-tri-benzyl-2-deoxy-2-N-(2,2,3,3,4,4,4-heptafluorobutanoyl)-α-D-glucopyranose 
• 1423122-13-7 C₃₈H₄₈N₂O₈ 
• 242142-78-5 methyl 2-[(tert-butoxycarbonyl)amino]-3,4,6-tri-O-benzyl-2-deoxy-α-D-glucopyranoside 
• 242142-78-5 Methyl 2-amino-3,4,6-tri-O-benzyl-2-deoxy-α-D-glucopyranoside 
• 960008-71-3 methyl 2-deoxy-3,4,6-tri-O-benzyl-2-(N-acetyl-N-tert-butyloxycarbonylamino)-α-D-glucopyranoside 
• 175875-14-6 methyl 2--3,4,6-tri-O-benzyl-2-deoxy-α-D-glucopyranoside 

Relevant articles and documents

Efficient syntheses of methyl 2-amino-2-deoxy-3,4,6-tri-o-benzyl-α-D-glucopyranoside and its 2-tert-butoxycarbonylamino- and 2-methylamino derivatives from N-acetyl-D-glucosamine

The synthesis of the title compounds started with N-acetylglucosamine which was converted into the corresponding methyl glycoside and O-protected with benzyl groups. Subsequent N-protection as its N-BOC-N-acetyl derivative and sequential removal of the N-

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

Glucosamine derivatives have been synthesized starting from commercially available N-acetyl-D-glucosamine/glucosamine hydrochloride and have been employed successfully as efficient organocatalysts for the direct asymmetric aldol reaction between cyclohexa

26. A 1H-NMR spectroscopic investigation of the conformation of the acetamido group in some derivatives of N-acetyl-D-allosamine and -D-glucosamine

The population of the conformations obtained by rotation around the C(2)-N and the N-C(O) bonds of AllNAc, GlcNAc, and GlcNMeAc derivatives was investigated by 1H-NMR spectroscopy. The AllNAc-derived α -D- and β -D-pyranosides 4-7, the AllNAc d