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

• 492-61-5 β-D-glucose 
• 100-39-0 benzyl bromide 
• 27851-29-2 benzyl 2,3,4-tri-O-benzyl-D-glucopyranoside 
• 1492828-89-3 benzyl 2,2,2-trifluoro-N-(4-nitrophenyl)acetimidate 
• 100-51-6 benzyl alcohol 
• 80300-30-7 1-O-acetyl-2,3,4,6-tetra-O-benzyl-D-glucopyranose 
• 4291-69-4 2,3,4,6-Tetra-O-benzyl-D-glucopyranose 
• 84799-77-9 methyl 2,3,4,6-tetra-O-benzyl-D-glucopyranoside 
• 74808-09-6 2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl trichloroacetimidate 
• 1927-62-4 tetrahydro-2-(benzyloxy)-2H-pyran 
• 53691-70-6 4,6-O-isopropylidene-D-glucopyranose 
• 1194045-30-1 but-2-ynyl 2,3,4,6-tetra-O-benzyl-β-D-galactopyranoside 
• 3866-62-4 2,3,4,6-tetrakis-O-(phenylmethyl)-1-O-acetyl-α-D-galactopyranose 
• 53081-30-4 tetra-O-benzyl-α-D-galactosyl bromide 

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 
• 1393113-98-8 C₃₈H₄₀O₉ 
• 61277-58-5 ((2R,3R,4S,5R)-3,4,5,6-tetraki s(benzyloxy)tetrahydro-2H-pyran-2-yl)methanol 
• 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 
• 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

New class of alkynyl glycoside analogues as tyrosinase inhibitors

A new series of alkynyl glycoside analogues were designed and synthesized from cheap and a commercially available sugar by introduction of various alkynyl and alkyl groups at C-1 and C-6 positions of the sugar ring. The inhibitory abilities of alkynyl gly

Direct dehydrative glycosylation catalyzed by diphenylammonium triflate

Methods for direct dehydrative glycosylations of carbohydrate hemiacetals catalyzed by diphenylammonium triflate under microwave irradiation are described. Both armed and disarmed glycosyl-C1-hemiacetal donors were efficiently glycosylated in moderate to excellent yields without the need for any drying agents and stoichiometric additives. This method has been successfully applied to a solid-phase glycosylation.

β-Selective Glycosylation by Using O-Aryl-Protected Glycosyl Donors

New glycosyl donors have been developed that contained several para-substituted O-aryl protecting groups and their stereoselectivity for the glycosylation reaction was evaluated. A highly β-selective glycosylation reaction was achieved by using thioglycosides that were protected by 4-nitrophenyl (NP) groups, which were introduced by using the corresponding diaryliodonium triflate. Analysis of the stereoselectivities of several glycosyl donors indicated that the β-glycosides were obtained through an SN2-type displacement from the corresponding α-glycosyl triflate. The NP group could be removed by reduction of the nitro group and acylation, followed by oxidation with ceric ammonium nitrate (CAN).