738518-26-8

Basic information

• Product Name: Benzyl 2-Amino-2-deoxy-α-D-galactopyranoside
• Synonyms: Benzyl 2-Amino-2-deoxy-α-D-galactopyranoside;PhenylMethyl 2-AMino-2-deoxy-α-D-galactopyranoside;Benzyl 2-amino-2-deoxy-a-D-galactopyranoside
• CAS NO: 738518-26-8
• Molecular Formula: C13H19NO5
• Molecular Weight: 269.29366
• Product Categories: Aromatics;Carbohydrates & Derivatives
• Mol File: 738518-26-8.mol
• Article Data: 15

Chemical Properties

• Appearance: /
• Solubility: Methanol
• CAS DataBase Reference: Benzyl 2-Amino-2-deoxy-α-D-galactopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: Benzyl 2-Amino-2-deoxy-α-D-galactopyranoside(738518-26-8)
• EPA Substance Registry System: Benzyl 2-Amino-2-deoxy-α-D-galactopyranoside(738518-26-8)

Safety Data

• Hazardous Substances Data: 738518-26-8(Hazardous Substances Data)

Upstream product

• 112146-85-7 benzyl 2-deoxy-2-<(4,4-dimethyl-2,6-dioxocyclohexylidenemethyl)amino>-α-D-glucopyranoside 
• 13343-62-9 benzyl 2-acetamido-2-deoxy-α-D-glucopyranoside 
• 221687-36-1 benzyl 2-deoxy-2-[1-(1,3-dimethyl-2,4,6(1H,3H,5H)-trioxopyrimidin-5-ylidene)phenylmethylamino]-α-D-glucopyranoside 
• 109-73-9 N-butylamine 
• 95451-81-3 Benzyl-2-azido-2-desoxy-α-D-mannoopyranosid 
• 95451-93-7 3,4,6-Tri-O-acetyl-2-azido-2-deoxy-α-D-mannopyranosyl bromide 
• 68733-20-0 1,3,4,6-tetra-O-acetyl-2-azido-2-deoxy-α-D-mannopyranoside 
• 95451-80-2 Benzyl-3,4,6-tri-O-acetyl-2-azido-2-desoxy-α-D-mannopyranosid 
• 100-51-6 benzyl alcohol 
• 2873-29-2 D-glucal triacetate 
• 22323-61-1 Methyl 3,4,6-tri-O-methyl-β-D-galactopyranoside 
• 110911-55-2 Methyl 2-O-allyl-3,4,6-tri-O-methyl-β-D-galactopyranoside 
• 110911-48-3 methyl-2-O-(N-imidazolylsulfonyl)-3,4,6-tri-O-methyl-β-D-galactopyranoside 
• 80035-31-0 benzyl 2-phthalimido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranoside 

Downstream Products

• 117701-85-6 ((2S,3R,4R,5S,6R)-4,5-Diacetoxy-6-acetoxymethyl-2-benzyloxy-tetrahydro-pyran-3-yl)-trimethyl-ammonium; bromide 
• 110911-57-4 benzyl-2-acetamido-3,4,6-tri-O-acetyl-2-desoxy-α-D-talopyranoside 
• 10375-65-2 benzyl 3,4,6-tri-O-acetyl-2-acetylamino-2-deoxy-α-D-glucopyranoside 
• 10375-65-2 benzyl 2-acetamido-3,4,6-tri-O-acetyl-2-deoxy-β-D-glucopyranoside 

Relevant articles and documents

Anti-cancer properties and catalytic oxidation of sulfides based on vanadium(V) complexes of unprotected sugar-based Schiff-base ligands

In this article, benzyl 2-deoxy-2-salicylideneamino-α-D-glucopyranoside (H2SalHGlc), a sugar-based Schiff-base ligand, as well as four of its derivatives including H2Sal5-BrGlc, H2Sal3,5-tBu/sup

Direct glycosylation of unprotected and unactivated sugars using bismuth nitrate pentahydrate

Bi(NO3)3, a low-cost, mild, and environmentally green catalyst, has been successfully utilized for Fischer glycosylation for the synthesis of alkyl/aryl glycopyranosides by reacting unprotected sugars, namely, D-glucose, L-rhamnose, D-galactose, D-arabinose, and N-acetyl-D-glucosamine with various alcohols in good to excellent yields. The glycosides were formed with high α-selectivity. Further, an expedient separation of α- and β-glycosides using silver nitrate-impregnated silica gel flash liquid chromatography has been developed.

Cross-functionalities of Bacillus deacetylases involved in bacillithiol biosynthesis and bacillithiol-S-conjugate detoxification pathways

BshB, a key enzyme in bacillithiol biosynthesis, hydrolyses the acetyl group from N-acetylglucosamine malate to generate glucosamine malate. In Bacillus anthracis, BA1557 has been identified as the N-acetylglucosamine malate deacetylase (BshB); however, a