158349-18-9

Basic information

• Product Name: 2,3,4,6-tetra-O-benzyl-D-galactonamide
• Synonyms: 2,3,4,6-tetra-O-benzyl-D-galactonamide
• CAS NO: 158349-18-9
• Molecular Weight: 555.671
• Mol File: 158349-18-9.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: 2,3,4,6-tetra-O-benzyl-D-galactonamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2,3,4,6-tetra-O-benzyl-D-galactonamide(158349-18-9)
• EPA Substance Registry System: 2,3,4,6-tetra-O-benzyl-D-galactonamide(158349-18-9)

Safety Data

• Hazardous Substances Data: 158349-18-9(Hazardous Substances Data)

Upstream product

• 214490-83-2 α,β-allyloxy-2,3,4,6-tetra-O-benzyl-d-galactose 
• 2595-07-5 allyl D-galactopyranoside 
• 10257-28-0 D-Galactose 
• 108-24-7 acetic anhydride 
• 6386-24-9 2,3,4,6-tetra-O-benzyl-D-galactopyranose 
• 82598-84-3 2,3,4,6-tetra-O-benzyl-D-galactonolactone 

Downstream Products

• 1438996-96-3 3,5-dibenzyloxy-6-benzyloxymethyl-2-pyridone 
• 158349-22-5 5-hydroxy-2,3,4,6-tetra-O-benzyl-δ-lactam 
• 158349-25-8 (3R,4S,5S,6R)-3,4,5-tris(benzyloxy)-6-((benzyloxy)methyl)piperidin-2-one 
• 570384-83-7 2-Nitro-N-((2S,3R,4S,5R)-2,3,4,6-tetrakis-benzyloxy-5-hydroxy-hexyl)-benzenesulfonamide 
• 570385-02-3 (2S,3S,4R,5S)-3,4,5-Tris-benzyloxy-2-benzyloxymethyl-1-(2-nitro-benzenesulfonyl)-piperidine 
• 570384-64-4 (2R,3S,4R,5S)-6-Amino-1,3,4,5-tetrakis-benzyloxy-hexan-2-ol 

Relevant articles and documents

An unusual synthesis of 2-pyridone and 3,5-dihydroxypyridine from a carbohydrate

An unusual aromatization to perbenzylated 3,5-dihydroxy-6-(hydroxymethyl)- 2-pyridone was demonstrated utilizing sugar lactam, under strong basic conditions, derived from d-Galactose. 2-Pyridone was efficiently converted into a pharmaceutically relevant s

Direct oxidative amidation of aldoses by iodine in ammonia water

Aldopentoses, aldohexoses and the benzylated derivatives reacted with iodine in ammonia water at room temperature to give their corresponding saccharide amides in high yields. The reactions proceeded with oxidation of the aldose hemiacetals by iodine to g

Glycosylidene carbenes: Part 32: Reaction of glycosylidene diaziridines with acylating and sulfonylating agents

Acylation and sulfonylation of the N,N'-unsubstituted glucosylidenespirodiaziridines 1A/1B 95:5 with Ac2O, BzCl, FmocCl, TsCl, (naphthalen-2-yl)sulfonyl, and (2,4,6-triisopropylphenyl)sulfonyl chloride, and concomitant rearrangement gave the ac