67890-29-3

Basic information

• Product Name: benzyl 2,3,4,6-tetra-O-benzyl-β-D-gluco-pyranoside
• Synonyms: benzyl 2,3,4,6-tetra-O-benzyl-β-D-gluco-pyranoside
• CAS NO: 67890-29-3
• Molecular Weight: 630.781
• Mol File: 67890-29-3.mol
• Article Data: 37

Chemical Properties

• CAS DataBase Reference: benzyl 2,3,4,6-tetra-O-benzyl-β-D-gluco-pyranoside(CAS DataBase Reference)
• NIST Chemistry Reference: benzyl 2,3,4,6-tetra-O-benzyl-β-D-gluco-pyranoside(67890-29-3)
• EPA Substance Registry System: benzyl 2,3,4,6-tetra-O-benzyl-β-D-gluco-pyranoside(67890-29-3)

Safety Data

• Hazardous Substances Data: 67890-29-3(Hazardous Substances Data)

Upstream product

• 100-44-7 benzyl chloride 
• 10343-13-2 benzyl-2,3,4,6-tetra-O-acetyl-β-D-glucopyranoside 
• 84799-77-9 methyl 2,3,4,6-tetra-O-benzyl-D-glucopyranoside 
• 4291-69-4 2,3,4,6-Tetra-O-benzyl-D-glucopyranose 
• 74808-09-6 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl trichloroacetimidate 
• 100-51-6 benzyl alcohol 
• 211678-08-9 p-methylphenyl 2,3,4,6-tetra-O-benzyl-1-thio-β-D-galactopyranoside 
• 100-39-0 benzyl bromide 
• 4304-12-5 benzyl β-D-galactopyranoside 
• 572-09-8 2,3,4,6-tetra-O-acetyl-D-glucopyranosyl bromide 
• 604-69-3 β-D-glucose pentaacetate 
• 53691-70-6 4,6-O-isopropylidene-D-glucopyranose 
• 80300-30-7 1-O-acetyl-2,3,4,6-tetra-O-benzyl-D-glucopyranose 
• 1927-62-4 tetrahydro-2-(benzyloxy)-2H-pyran 

Downstream Products

• 35094-65-6 1,6-di-O-acetyl-2,3,4-tri-O-benzyl-β-D-glucopyranoside 
• 4356-77-8 acetyl 6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranoside 
• 566905-73-5 benzyl 2,3,4-tri-O-benzyl-β-D-glucopyranoside 6-(hydrogen succinate) 
• 6564-72-3 2,3,4,6-tetra-O-benzyl-D-glucopyranose 
• 59531-24-7 2,3,4,6-tetra-O-benzyl-D-glucopyranoside 
• 85339-00-0 benzyl-6-O-acetyl-2,3,4-tri-O-benzyl-α-D-glucopyranoside 
• 27851-30-5 benzyl 6-O-acetyl-2,3,4-tri-O-benzyl-β-D-gluco-pyranoside 
• 61277-58-5 ((2R,3R,4S,5R)-3,4,5,6-tetraki s(benzyloxy)tetrahydro-2H-pyran-2-yl)methanol 
• 1393113-98-8 C₃₈H₄₀O₉ 
• 27851-29-2 benzyl 2,3,4-tri-O-benzyl-D-glucopyranoside 
• 4291-69-4 2,3,4,6-Tetra-O-benzyl-D-glucopyranose 
• 4132-31-4 penta‐O‐benzyl-α-D‐glucopyranoside 
• 6386-24-9 2,3,4,6-tetra-O-benzyl-D-galactopyranose 

Relevant articles and documents

Synthesis of photolabile group protected anomeric acetals and its application in carbohydrate synthesis with the assistance of continuous flow photo-reactor

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An Unexpected FeCl 3/C-Catalyzed β-Stereoselective Glycosylation in the Presence of the C(2)-Benzyl Group

An efficient and completely β-stereoselective glycosylation that did not rely on neighboring group participation is described using 2-20 molpercent FeCl 3 /C as the catalyst and benzylated propargyl glycosides as the donors to reach yields up to 96percent under mild condition. With an octatomic-ring intermediate at the α-face of FeCl 3 /C with alkyne of propargyl glycosides, a panel of aglycones comprising aliphatic, alicyclic, unsaturated alcohols, halogenated alcohols, and phenols with different substitution were examined successfully for the exclusive β-stereoselective glycosylation reaction.