142719-06-0

Basic information

• Product Name: methyl 2,3,4-tri-O-benzyl-6-O-(4-methoxybenzyl)-α-D-glucopyranoside
• Synonyms: methyl 2,3,4-tri-O-benzyl-6-O-(4-methoxybenzyl)-α-D-glucopyranoside
• CAS NO: 142719-06-0
• Molecular Weight: 584.709
• Mol File: 142719-06-0.mol

Chemical Properties

• CAS DataBase Reference: methyl 2,3,4-tri-O-benzyl-6-O-(4-methoxybenzyl)-α-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 2,3,4-tri-O-benzyl-6-O-(4-methoxybenzyl)-α-D-glucopyranoside(142719-06-0)
• EPA Substance Registry System: methyl 2,3,4-tri-O-benzyl-6-O-(4-methoxybenzyl)-α-D-glucopyranoside(142719-06-0)

Safety Data

• Hazardous Substances Data: 142719-06-0(Hazardous Substances Data)

Upstream product

• 53008-65-4 methyl 2,3,4-tri-O-benzyl-D-glucopyranoside 
• 89238-99-3 O-(4-methoxybenzyl)-trichloroacetimidate 
• 105-13-5 4-Methoxybenzyl alcohol 
• 1450734-54-9 4-methoxybenzyl N-phenyl-2,2,2-trifluoroacetimidate 
• 824-94-2 p-methoxybenzyl chloride 

Downstream Products

• 1338712-10-9 methyl 2,3,4-tri-O-benzyl-6-O-(2,3,4-tri-O-benzoyl-6-O-pentenoyl-β-D-glucopyranosyl)-α-D-glucopyranoside 
• 128503-39-9 methyl 2,3,4-tri-O-benzoyl-6-O-(2,3,4,6-tetra-O-benzoyl-D-glucopyranosyl)-α-D-glucopyranoside 
• 53008-65-4 methyl 2,3,4-tri-O-benzyl-D-glucopyranoside 
• 176168-90-4 1-anhydro-2,3-bis-O-benzyl-α-D-glucopyranoside 

Relevant articles and documents

P-Methoxybenzyl-N-phenyl-2,2,2-trifluoroacetimidate: A versatile reagent for mild acid catalyzed etherification

PMB-NPTFA 1a is a new month bench stable and powerful reagent for the formation of PMB ethers. Several alcohols were protected in high yields and short reaction times, using low reagent loading and small catalytic amounts of Bi(OTf)3. The mild

Reverse orthogonal strategy for oligosaccharide synthesis

Herein, we report the invention of a novel expeditious concept for oligosaccharide synthesis. Unlike the classic orthogonal strategy based on leaving groups, the reverse approach is based on orthogonal protecting groups, herein p-methoxybenzyl and 4-pentenoyl, which allows for efficient oligosaccharide assembly in the reverse direction.