615564-29-9

Basic information

• Product Name: 4-methoxybenzyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside
• Synonyms: 4-methoxybenzyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside
• CAS NO: 615564-29-9
• Molecular Weight: 660.807
• Mol File: 615564-29-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 4-methoxybenzyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: 4-methoxybenzyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside(615564-29-9)
• EPA Substance Registry System: 4-methoxybenzyl 2,3,4,6-tetra-O-benzyl-α-D-glucopyranoside(615564-29-9)

Safety Data

• Hazardous Substances Data: 615564-29-9(Hazardous Substances Data)

Upstream product

• 74808-09-6 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl trichloroacetimidate 
• 105-13-5 4-Methoxybenzyl alcohol 
• 80300-30-7 1-O-acetyl-2,3,4,6-tetra-O-benzyl-D-glucopyranose 

Downstream Products

• 615564-31-3 (2R,3R,4R,5R,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-((2R,3R,4S,5R,6R)-3,4,5-tris-benzyloxy-6-benzyloxymethyl-tetrahydro-pyran-2-yloxy)-tetrahydro-pyran-3-ol 
• 99-20-7 TREHALOSE 

Relevant articles and documents

Electron-deficient pyridinium salts/thiourea cooperative catalyzed O-glycosylation via activation of O-glycosyl trichloroacetimidate donors

The glycosylation of O-glycosyl trichloroacetimidate donors using a synergistic catalytic system of electron-deficient pyridinium salts/aryl thiourea derivatives at room temperature is demonstrated. The acidity of the adduct formed by the 1, 2-addition of

Formation of 1,1-α, α-glycosidic bonds by intramolecular aglycone delivery. A convergent synthesis of trehalose

(Matrix presented) We report a new synthesis of trehalose analogs that involves the use of intramolecular aglycone delivery for stereoselective formation of the 1,1-α,α-glycosidic bond. The glycosylation reaction afforded the desired isomer exclusively and in good yield.